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The first edition won first prize in Anaesthesia in the 2019 BMA Medical Book Awards!Here's what the reviewers said:"It is so easy to pick up and check things, and the illustrations and drawing instructions have allowed me to do my own drawings and learn how to label them."This new edition has been thoroughly revised and updated, and continues to provide you with simple instructions on how to draw and interpret the crucial anatomy you need for your anaesthetic training. Covers all the relevant anatomy in:Head, neck and neuro – from Circle of Willis to cervical plexusVertebral column – from the spinal cord to the sacrumCardiac – coronary arteries and venous drainage of the heartAirway and respiratory – from airway sensation to the diaphragmAbdomen – from the abdominal aorta to the nephron, via a TAP blockLimbs – from blood vessels in the arms to the ankle, via the femoral canalFor the majority of sections, in addition to a simple drawing and detailed explanation, there are also step-by-step illustrations to show you how to draw the anatomy yourself – taking some of the stress out of potential viva questions!

This book covers the key techniques that can be employed in any lab with access to cell imaging equipment, even if it does not currently specialize in imaging. It focuses on live cell imaging and light microscopy applications, but is equally relevant to the imaging of fixed specimens.

Whole genome amplification generates microgram quantities of genomic DNA starting from a sample of as little as a few femtograms and so is a vital technique when sample material is limited, as well as for high-throughput assays. Whole Genome Amplification: Methods Express is a comprehensive up-to-date laboratory manual for this key technique. It provides detailed step-by-step protocols as well as hints and tips for success and troubleshooting, taking readers through all aspects of whole genome amplification. This book is an essential practical guide for any researcher currently using PCR for genomic amplification or who wishes to do so in future.

Proteomics: Methods Express identifies the most powerful new technologies and presents them in a way that allows their robust implementation. The focus is on proteomic methods and strategies that are reliable and of general applicability. Each chapter presents descriptions of what can, and cannot, be achieved with the relevant procedures so that readers can make informed judgments prior to establishing the methods in-house. Every chapter discusses the merits and limitations of various approaches then provides tried-and-tested protocols with hints and tips for success and troubleshooting for when things go wrong.

DNA Microarrays: Methods Express covers the very latest in DNA microarray technology, with a clear focus on how these techniques can be used in the lab to gain the very best results. The authors are from some of the leading laboratories in the field and write with real authority on the latest methodology. Every chapter provides detailed step-by-step protocols with valuable hints and tips for success, as well as giving typical experimental results and selected literature citations. This book is a 'must have' manual for researchers in all fields of biology, medicine and agriculture.

Whole genome amplification generates microgram quantities of genomic DNA starting from a sample of as little as a few femtograms and so is a vital technique when sample material is limited, as well as for high-throughput assays.Whole Genome Amplification: Methods Express is a comprehensive up-to-date laboratory manual for this key technique. It provides detailed step-by-step protocols as well as hints and tips for success and troubleshooting, taking readers through all aspects of whole genome amplification. This book is an essential practical guide for any researcher currently using PCR for genomic amplification or who wishes to do so in future.

Proteomics: Methods Express identifies the most powerful new technologies and presents them in a way that allows their robust implementation.The focus is on proteomic methods and strategies that are reliable and of general applicability. Each chapter presents descriptions of what can, and cannot, be achieved with the relevant procedures so that readers can make informed judgments prior to establishing the methods in-house.Every chapter discusses the merits and limitations of various approaches then provides tried-and-tested protocols with hints and tips for success and troubleshooting for when things go wrong.

DNA Microarrays: Methods Express covers the very latest in DNA microarray technology, with a clear focus on how these techniques can be used in the lab to gain the very best results. The authors are from some of the leading laboratories in the field and write with real authority on the latest methodology. Every chapter provides detailed step-by-step protocols with valuable hints and tips for success, as well as giving typical experimental results and selected literature citations.This book is a 'must have' manual for researchers in all fields of biology, medicine and agriculture.

Bioinformatics: Methods Express is unique. It is a book on bioinformatics that makes sense to non-bioinformaticians.Bioinformatics: Methods Express helps you answer common questions such as: *what else is similar to my gene?*does this protein have any transmembrane regions?*how do I visualize an alignment between these DNAs?*where can I find specific transcription factor sequences?The book provides the clear advice and explicit protocols that non-bioinformaticians need in order to understand what to do - and how to avoid common pitfalls. Each chapter guides you through the major databases and tools with worked examples - all accompanied by sample data files available online.Topics covered include:*data access*sequence searches and alignments*identification and annotation of features*the transcriptome*protein structure and function*comparisons and phylogenyBioinformatics: Methods Express is a comprehensive manual for all wet-bench scientists who need to use bioinformatics - from postgraduate student to principal investigator.www.scionpublishing.com/bioinformatics contains comprehensive datasets which allow the reader to practise the techniques described in the book.

Getting into GP Training is a practical guide for anyone planning to become a GP and so looking to enrol in a GP Specialty Training Programme.Uniquely, this book covers all stages of the application process, from the initial longlisting and application to a General Practice Deanery (Stage 1), through the computer-based tests at Stage 2, the selection tests at Stage 3, and allocation to a Deanery (Stage 4).Written by an author who has recently been through the whole application process himself, this book includes full practice papers for the Stage 2 and 3 exams. It is packed full of hints and tips for all stages of the application process to help the reader succeed in the application process and enter the training programme of their choice.

This book covers the key techniques that can be employed in any lab with access to cell imaging equipment, even if they do not currently specialize in imaging. It focuses on live cell imaging and light microscopy applications, but is equally relevant to the imaging of fixed specimens.

This glycobiology book is truly unique. Produced to commemorate the 80th birthday of Nathan Sharon, Glycobiology is an essential reference tool for anyone working in the field. Most research review volumes are narrowly focused. This book is different. It is a state-of-the-art fully comprehensive review volume covering a deliberately wide spectrum of work in this important field. With 28 chapters, covering over 350 pages, this title describes the latest research findings - from chemistry to biology and from pure science to industrial and medical applications.The book is written by world-class researchers and brings the reader fully up-to-date with the latest advances and forward thinking. All the major areas of glycobiology are covered including the synthesis of carbohydrates and glycoconjugates, their structural and functional analysis, carbohydrate binding proteins, carbohydrate modifying enzymes, and the applications of glycobiology research in medicine and industry. All active researchers in the glycosciences will value access to this important research compendium whether it be in the local library or in the lab.

PCR is the most widely used technique in molecular biology. New PCR variants offering substantial benefits to existing protocols appear on a frequent basis. PCR: Methods Express describes the very latest PCR-based methodologies and approaches to provide the most up-to-date practical advice on how to tackle a broad range of biological problems including:*real time qRT-PCR*rapid generation of gene targeting constructs*PCR multiplexes*PCR-based mutagenesis*identification of microdeletions and microduplications*DNA methylation analysis*forensic genetic DNA typing*genotyping*identification of mutations in single cells*whole genome amplification*diagnosis of infectious diseases*inverse PCR-based RFLPThis book is a comprehensive research guide; every chapter discusses the merits and limitations of the available approaches and then provides fully-proven protocols with hints and tips for success. PCR: Methods Express is an essential laboratory manual for researchers in all life science fields and at all levels, from postgraduate student to principal investigator.

This fully-revised edition of Haematology is written in an approachable style that focuses on improving understanding and encourages students to think around the subject. The numerous illustrations and defined learning objectives are designed to aid effective learning, while the many 'fast facts' boxes broaden the interest and perspective of the material. Further reading lists and website information guide students to more detailed coverage if required. This book will be useful for undergraduate and postgraduate students of haematology, as well as medical students and those embarking on higher professional qualifications. From reviews:'...This haematology textbook seems to achieve the impossible: it is short in length, broad in scope and yet does not restrict itself to basic facts. Its other great strength is an extremely readable, clear and consistent prose. This makes it stand out from textbooks compiled by editors but where different authors contribute each chapter...'Royal College of Pathologists Bulletin number 157, January 2012

There have been a number of significant changes in transfusion science in the last five to ten years and this second edition of Transfusion Science covers these in some detail.* A new chapter introduces readers to the current applications of emerging techniques in transfusion science.* Platelet immune disorders and haemolytic anaemias are now covered.* The need for leucodepletion and methods for pathogen reduction are described.* The latest nomenclature for blood group genes has been adopted.* Current practice in blood group serology is reviewed.* Recent legislative changes for quality assurance in transfusion in the UK are now also covered.Case studies and colour photographs are now provided to illustrate concepts and to aid understanding, and a revised series of self-assessment questions and learning outcomes are also provided.An understanding of transfusion science is vital for all biomedical science students. Transfusion Science, second edition, explains all the basic principles alongside descriptions of the applications now possible as a result of modern analytical techniques. This book is essential reading for all students studying courses on transfusion and transplantation.

Clinical Biochemistry, second edition, is essential reading for all students studying clinical biochemistry, especially those on biomedical science courses. The book concentrates on the areas of body function required for the maintenance of health. These include: inputcontrolprocessingtransport and storagedefence and output Each chapter provides an introduction to pathophysiology; how biochemical changes arise as a result of disease processes. The book also describes the important methods used in clinical biochemistry laboratories to show how biochemical changes are measured and how they change during disease. This edition has been substantially revised to incorporate the latest developments in genomics, proteomics and biosensors. The book also benefits from an improved design and layout to aid student understanding.

Protein expression is an increasingly important tool for research on gene function. What is needed is not just a lab manual providing established methods as well as the latest state-of-the-art protocols, but also clear advice on what expression system to choose when. Expression Systems: Methods Express uniquely fills this need. It covers expression across a broad range of systems, including the following:Baculovirus expression vectorsCHO cellsE. coliHEK293-EBNA1 cellsLactococcus lactis and other gram positive bacteriaS. cerevisiaeTransfected insect cellsPichia pastorisMammalian cells using BacMam virusesLentiviral vectorsWheat germ cell-free systemThe book takes the reader through how to make an informed choice of appropriate system, taking into account the protein target, the time involved, the ultimate use of the expressed protein, and the laboratory equipment required. It also provides step-by-step methods for each system. In addition, the book describes the optimisation of expression strategies, expression engineering using ribosome display, and how to select protein variants with improved expression.Every chapter discusses the merits and limitations of the approaches available, describes the key techniques in full practical detail, and provides sensible advice for immediate use at the bench.In summary, Expression Systems: Methods Express is a comprehensive laboratory manual and information resource for researchers at all levels, from postgraduate student to principal investigator.

Protein expression is an increasingly important tool for research on gene function. What is needed is not just a lab manual providing established methods as well as the latest state-of-the-art protocols, but also clear advice on what expression system to choose when. Expression Systems: Methods Express uniquely fills this need. It covers expression across a broad range of systems, including the following. *Baculovirus expression vectors*CHO cells* E. coli*HEK293-EBNA1 cells* Lactococcus lactis and other gram positive bacteria* S. cerevisiae*transfected insect cells* Pichia pastoris*mammalian cells using BacMam viruses*lentiviral vectors*wheat germ cell-free systemThe book takes the reader through how to make an informed choice of appropriate system, taking into account the protein target, the time involved, the ultimate use of the expressed protein, and the laboratory equipment required. It also provides step-by-step methods for each system. In addition, the book describes the optimisation of expression strategies, expression engineering using ribosome display, and how to select protein variants with improved expression. Every chapter discusses the merits and limitations of the approaches available, describes the key techniques in full practical detail, and provides sensible advice for immediate use at the bench. In summary, Expression Systems: Methods Express is a comprehensive laboratory manual and information resource for researchers at all levels, from postgraduate student to principal investigator.

Physics: A Student Companion offers readers a thorough overview of basic physics with rapid access to fundamental concepts and their derivations. Covering the core fields of mechanics and relativity, electromagnetism, waves and optics, quantum mechanics, and thermal physics, this book is an essential learning tool for students, as well as a handy reference for graduates and researchers in the physical sciences. The perfect companion to the mainstream physics textbooks, providing fast access to the essential material Highlights and consolidates the key equations, derivations, theories and concepts that are the fundamentals of your physics course Provides a structured outline of the core ideas, to be used alongside lecture notes and classes Offers an ideal reference for graduates and researchers in the physical sciencesInformal style –  written by a recent student specifically for students Notes are used to highlight the major equations, show where they come from and how they can be used and applied The aim is to consolidate understanding, not teach the basics from scratch If you are looking for a better option than digging through college textbooks for that forgotten something, reviewing material for an examination, or preparing for graduate entry, then Physics:  A Student Companion is the right book for you. From reviews:"Every undergraduate physicist ought to own a copy of this remarkable, unique and innovative textbook... I truly believe this textbook should be taken advantage of by all undergraduates, and I wish it had been published earlier in my undergraduate degree."Student Review, Times Higher Education, May 2012

Based on their extensive experience of clinical work, the authors emphasize the practical issues related to the healthcare of individuals and families. Genetics for the Health Sciences takes an holistic approach, from preconception to adulthood, and addresses the false notion that clinical genetics is of relevance only to those who are planning a family.The book enables nurses, midwives, genetic counselors and doctors to apply the general principles of genetics in their routine clinical practice.As well as discussing the basic principles, Genetics for the Health Sciences also describes the latest technologies and shows how these can be applied to clinical practice.This is an essential text which helps all those in clinical healthcare understand the genetics they need in their professional roles. It is also an ideal coursebook for students in the healthcare professions seeking an understanding of core genetic principles and how these are applied in practice.Reviews:'The text is a compact, concise presentation of the basic concepts in genetics science and the impact of genetics across the lifespan. The organization of the text increases its usefulness to clinicians as each specialty area could easily locate the information most pertinent to their work...The text is well illustrated throughout, again providing summarized information that is easily accessed. An especially helpful feature of this text is the presence of multiple case studies in each chapter, making this text particularly useful for teaching. I think faculty teaching students in advanced practice nursing programs and allied health courses would find this text a succinct addition to their course. However, I could also see this text being useful in RN preparation curriculum. It could easily be a text that would carry over for several specialty areas and provide additional material specific to genetics in each area.Genetics for Health Sciences: A Handbook for Clinical Healthcare  is a welcome addition to the rather sparse choices available for presenting genetics content in clinical practice curriculum.Rebekah Hamilton, ISONG, June 2010'Tremendous progress in recent years has shaped the field of medical genetics, which continues to expand to involve almost every aspect of human health. Hence, it is necessary for every healthcare professional to acquire a basic understanding of this science. This is clearly the objective of this well-edited and structured book by Skirton and Patch in its second updated edition. The authors' considerable experience in genetics, through direct clinical practice in addition to organisational and academic roles, can be appreciated in the practical aspect of their writing. The book starts with useful definitions and alerts the reader to the wide applicability of genetics through clinical cases, raising questions that are answered and discussed when relevant in later chapters. Important aspects of genetic counselling, from basic skills such as risk estimation using family trees to more complex ones related to effective ethical communication with the clients in the light of their needs and the different models of counselling, are then discussed in two chapters. However, given their intrinsic function in medical genetics, these issues are also efficiently tackled in the clinical cases outlined in each chapter. The authors then describe important scientific concepts and techniques that are necessary for a good clinical understanding of genetics. Although this section may seem short, the additional resources provided at the end are very useful. Likewise, for all topics covered in the book, the updated links provided serve as a handy catalogue for the health professional seeking extra information. Next, the concepts and techniques described in the first part of the book are applied directly to common genetic conditions and issues faced by different age groups, from prenatal care to older adulthood in separate chapters. This organisation puts into perspective the importance of genetics in different medical specialities and settings. This book, with its concise yet comprehensive explanation of a complex rapidly growing field, should prove to be a valuable resource for a diverse audience of health professionals, including midwives, nurses and physicians, who confront genetic issues during their daily practice without being specialists in medical genetics.'Nadine Taleb, Journal of Medical Genetics'When first asked to write this book review I thought to myself how it would be important to give a rounded report on both the book’s strengths and weaknesses. After reading the book, however, I realised that it is difficult to find weaknesses.The authors, Heather Skirton and Christine Patch, between them have over 30 years of experience in clinical genetics.  Their experience of explaining genetics in their professional roles shines through in the way they have written the book.  They make complex genetic principles interesting and understandable. The book does not baffle or patronise.The book is easily navigated. It is broken down into clear chapters that are ordered in a pleasingly logical way. The first chapter 'sets the scene' by introducing the reader to important concepts related to genetic health care including issues such as ethical practice, the different forms of genetic testing and the impact of genetic conditions on families. The next chapters then discuss the family tree, counselling issues, genetic science and public health genetics. The remaining chapters then explore the core topics relating to particular life stages from preconception to older adulthood. It engages the reader from the start when it introduces seven ‘core’ families that reappear throughout the book to highlight a number of key issues.The text is peppered with clear illustrations, useful step by step guides, practical checklists, and test yourself sections making the book lively and dynamic. The test yourself sections make the book student friendly and would also make good teaching aids to lecturers and tutors. At the start of the book there is a list of helpful websites and at the end of each chapter there is a list of resources for those who wish to extend their knowledge.One of the main strengths of this book is its refreshingly practical approach. All too often books can be written in a way in which it is difficult for the reader to transfer the knowledge that they have gained into their day-to-day practice. The introduction states that 'the aim of this book is to enable those in healthcare to update their knowledge on topics related to genetics and genomics that have an impact in their daily work and apply it usefully in patient care'. Given the fact that genetics has increasingly become a core component in a number of specialties, one would think that meeting this aim for all would be a tall order. This book however eloquently does so using case examples and key practice points boxes throughout to demonstrate the clinical application of the topic under discussion. Another of the book’s main strengths is the way in which it promotes individualised care by enabling the reader to consider the impact of genetic conditions from the patients’ point of view.Genetics for the Health Sciences brings genetics into common healthcare settings. It is highly recommended as an essential text for health care professionals in roles across all specialties. It is also recommended to students, lecturers, social scientists; to anyone who has an interest in genetics and wishes to extend their knowledge. It is a joy to read and could be read from cover to cover.'Helen Thistlewood, Medical Genetics'Genetics is at the forefront of medicine and nurses are expected to have a basic understanding of the subject.This handbook is well written and the authors do a good job of making this complex topic understandable.The book lists prenatal, childhood and adult genetic conditions that may involve testing and counselling.Genetic services, types of genetic testing and the impact of genetic conditions on families are discussed in depth, and case studies highlight the emotional and psychological needs of patients and their families. Guidelines for drawing family trees and practical examples of risk assessment are well explained. The perspective of the patient regarding risk and lay knowledge is also considered... All departments should have a copy of this book on their shelves.'Audrey Ardern-Jones, Nursing Standard

Human Genetics 2e begins by describing basic human genetics, introduces the variety of techniques available for disease diagnosis and details how these are used in the lab, before concluding with information on prenatal diagnosis, genetic counselling and ethical considerations. As such, the book is the ideal handbook for biomedical science students and for anyone working in a diagnostic genetics lab. This second edition has been comprehensively rewritten to take into account the major changes in recent years, particularly with regard to human molecular genetics:greater coverage of recently identified genes and their role in diseaseupdated to include an expanded section on breast cancerexpanded description of epigenetics including methylation and acetylationupdated to include all the latest diagnostic tools: QF-PCR, MLPA, RT-PCR, microarrays, etc.more on the impact of genetics on society; ethics and dilemmasfull colour photographs have been included to allow readers to see real laboratory results If you need to know the difference between SNPs and CNVs, when to use QF–PCR or microarrays, or wondered which screening method to use for mutation detection, then you need to read this book. Reviews:"This revised edition of Human Genetics covers an impressive variety of topics within the field, and would certainly be suitable for an audience ranging from basic science undergraduates to people working within genetics in the medical profession...The material in this book is clearly laid out, and provides a comprehensive overview of the subject. The explicit list of learning objectives at the start of each chapter will be valued by students and teachers alike, and the explanatory sentence or two after each one provides a quick reference to the key take-home messages. Within the text, important facts and definitions are highlighted in boxes, and reinforced by straightforward and logical figures. The authors acknowledge that this is an introductory text, but also provide key references to further reading, enabling readers to easily expand their knowledge in specific areas of interest, yet achieving a fundamental grasp of the areas being presented. This further reading, along with the incredibly valuable self-assessment questions, will allow students to identify and address the limits of their knowledge.The emphasis on genetic disorders throughout the book will make it relevant to those studying the science of human genetics, but also to medical students throughout their studies. The glossary of disorders at the end of the book provides an excellent quick reference point, and the comprehensive list of internet sites directs the reader to many other well recognised resources for further information. In the age of information overload via the internet, such a list is incredibly valuable for helping students assess the quality of the information they are retrieving from online sources...This book will appeal to anyone with an interest in human genetics, particularly those approaching the subject from the point of view of a diagnostic laboratory."Dr Sally Chappell, IJMEG, April 2010"Advances in genetics are continually being made, and Human Genetics provides an overview of up to date practice within this field. It reviews the basics of DNA, different modes of inheritance and gene function. This volume takes the reader through the different techniques used in both molecular genetics and cytogenetic laboratories, concluding with the clinical aspects of genetics. All aspects are clearly explained using diagrams and photographs to achieve clarity and promote understanding.This book acts as a good reference and revision guide for those working in the genetics field or for those new to genetics. It would also be useful to undergraduates in biomedical sciences, providing a quick reference guide to complement other text books in the field of genetics, which individually study the different areas outlined in Human Genetics in more detail.Human Genetics is easily navigated with clear chapters broken down into individual sections. It allows the reader to dip in and out of the book as required, yet at the same time, ensures that each area can be studied in more detail. The quick reference guide of conditions at the back of the book will be of particular value for clinicians. It not only gives a brief outline of the clinical aspects of the different conditions, but it also clearly states which laboratory techniques are used in the diagnosis of each condition. This will be invaluable for any clinician requesting testing, but unsure exactly which test is needed, and therefore uncertain as to what sample should be taken from the patient. Although this book provides an overview, it does, however, point the reader in the right direction to find more information on each individual area both through further reading and internet resources.The chapter on mechanisms of disease may not be new to scientists, but for those working in the clinical field without a strong science background these concepts may be fairly new to them. Human Genetics will aid in their understanding of different conditions, and the reports issued enabling them to translate this in a clear manner to patients.Throughout the book clear illustrations are used to clarify the techniques described and complement the text. It is particularly helpful to have ‘true to life’ pictures when the authors have described certain techniques, such as raw DNA sequence information as well as some of the cancer genetics techniques. These can only be truly understood by seeing a realistic output of the data to be analysed.The book is clearly written from a scientific perspective and, although it touches on some of the aspects of clinical genetics, it is important to realise that this is only very brief. This is the weaker side of the book, and so anyone in the clinical field would certainly need to be exploring clinical issues further, particularly in relation to complex family issues and the psychosocial aspects of genetic counselling.This book would be a useful text for those studying biomedical sciences or a Masters course in genetic counselling. Although there is no great depth to the book, and students will need to look elsewhere for more comprehensive texts on particular aspects, it does bring together the laboratory and clinical aspects of genetics. It also traces the path from the original discussion with a patient, through sample extraction to the laboratory techniques as well as exploring the mechanisms underlying the origin of the relevant genetic changes."C. Kirwan, Human Genetics, vol. 128, August 2010"In order to evaluate a book one should know its intended audience. The preface to this book says that it, as was the first edition, should be relevant to first year undergraduates and newcomers to the medical profession; it is intended as an introduction to human genetics, to supplement other basic textbooks. The implication that the reader should already have a grounding in basic genetics is well founded. I doubt that the introductory chapters on cytogenetics (which gets into exons and introns) and molecular genetics would be understood without a previous grasp of the relation between the DNA triplet sequence  in a gene with the amino-acid sequence of the corresponding protein. The authors have done a commendable job of updating the remarkable advances in molecular genetics of the past few years, ranging from new epigenetic insights, through automated techniques for high through-put screening, to the use of microarrays in molecular cytogenetics. But scanning of the volume suggests that it would be more suitably directed to laboratory, rather than clinical geneticists. There is, for example,  a full page box listing the constituents of a culture medium, more suited to a lab manual than a text book. Nowhere does the book list the credentials of the authors, but a Google search reveals that Dr Davies is Head of Laboratories at the Southmead Hospital, Bristol, UK. Laboratory geneticists should find the sections on molecular cytogenetics (FISH, CGH), molecular genetics (Southern blotting, PCR), cancer genetics, and prenatal diagnosis particularly useful. Clinical geneticists may appreciate them as a source of information about what lies behind the reports of molecular diagnoses they receive from the laboratories. Clinical geneticists would be better off to turn to one of the other texts recommended at the ends of each chapter. Multifactorial inheritance gets short shrift, having only a few sentences in a section entitled “Gradation of Inheritance”. And multifactorial conditions are not in the list of reasons for referral  to genetic services – presumably because they usually do not engender requisitions for laboratory tests. The chapter on genetic counseling does not mention the use of empirical recurrence risks in genetic counseling, or include anything about its psychodynamics. There are remarkably few typographical errors (I only found one), and a few unclear or incorrect statements. The colored illustrations are of good quality, and some are beautiful, including that on the cover, but the black and white ones need some improvement. In recognition of our increasing predilection for abbreviations, the book begins with a useful two and a half page list of them."F. Clarke Fraser, American Journal of Medical Genetics, Part A, July 2010

Radiological imaging is now accessible to a wide range of healthcare workers, many of whom are increasingly taking on extended roles. This book will equip all healthcare professionals, including medical students, chest physicians, radiographers and radiologists, with the techniques and knowledge required to interpret plain chest radiographs. It is not an exhaustive text, but concentrates on interpretive skills and pattern recognition – these help the reader to understand the pitfalls and spot the clues that will allow them to correctly interpret the chest X-rays they will encounter in their daily practice. The book features over 300 high quality images, along with a range of case story images designed to enable readers to test and develop their interpretation skills. Interpreting Chest X-Rays is a handy ready reference that will help you to avoid making errors interpreting chest X-rays and decide, for example:if a temporary pacing wire has been inserted correctlywhether the shadows you can see are real abnormalitiesif all chest tubes and lines are located appropriately in an ITU patientwhat further imaging may assist interpretation of an apparent abnormalitywhether a post-surgical chest is significantly abnormalwhat organism might be causing an infectionwhy a patient is short of breathwhether patient positioning accounts for an abnormal appearance on a chest X-raywhat impact radiographic technique has had on the appearance of pathology From reviews:'Interpreting Chest X-Rays is highly recommended for anyone wishing to acquire a basic yet relatively comprehensive approach to the chest radiograph. The book is affordable, and is particularly suited for trainees, including pulmonary medicine fellows, medical students on a radiology rotation, physicians' assistant students or nursing students on a critical care or pulmonary rotation, and first-year radiology residents on a thoracic radiology rotation. Dr. Stephen Ellis makes the difficult seem easy, with his instructive teaching style and helpful approach to the surprisingly difficult topic of chest radiography interpretation.'Clinical Pulmonary Medicine, November 2010'Interpreting Chest X-Rays is an excellent, simple book...[it] is reasonably priced and would be recommended to all healthcare professionals who are involved with the interpretation of plain chest radiographs.'RAD Magazine, December 2010'Interpreting Chest X-Rays was a delight to read and review. It is a concise text that covers the basics of chest radiography. This book would be perfect for the medical student, allied health care worker, or general physician.'American Journal of Roentgenology, May 2011

HIGHLY COMMENDED IN THE BMA MEDICAL BOOK AWARDS 2013!Clinical Skills Explained guides readers through the clinical skills typically required at medical school. Most clinical skills books are either brief 'checklist-type' books, or very detailed physical examination books. Clinical Skills Explained is different; it covers the topic concisely to fit in with the needs of the modern medical student, but also provides enough background knowledge to ensure the reader knows the why as well as the how. The book is written in a clear logical style and covers:history takingclinical examinationsstandard procedures Each chapter starts by providing a short step-by-step guide to what you need to do (the ideal aide-memoire) then describes the background knowledge and relevant pathophysiology before moving on to a systematic approach on how to tackle the skill at hand. At all stages the text is supported by clear full colour diagrams to reinforce understanding. The authors also provide quick reminder boxes covering:top tipsmedical guidelinesdifferential diagnosesdiagnostic indicators To test your understanding, each chapter ends with a series of clinical scenarios that are typical of the cases you will come up against. These encourage you to assess the key features, consider the likely diagnosis, and decide what questions you might ask, or further investigations you might request, to confirm your diagnosis.From reviews:"With a philosophy that there is more to learning clinical skills than following checklists, this book offers students a clear, concise manual from which they can learn clinical skills and procedures in a systematic manner; whilst developing an understanding of not only what they need to do and why they need to do it, but also learn to apply key elements of theory to patient presentation and examination findings to generate differential diagnoses... This book will be extremely useful for students in the early stages of their training. By integrating clinical skills information with core basic scientific knowledge, it allows students to apply theory to practice as they develop essential clinical skills and basic problem solving skills."International Journal of Clinical Skills, 2013

Whether you are a student of biomedicine or medicine, trainee, resident, or endocrinology fellow, Clinical Endocrinology provides you with the core information you need to understand this notoriously complex subject.The book describes the biochemistry, physiology, and anatomy that underpin clinical practice and then integrates genuine clinical cases to show the application of this basic science in diagnosis and treatment.Key features include:a flowing narrative that leads you through the basic scienceboxes that provide core reference informationadvanced boxes that provide additional material suitable for residents and fellowscase studies that link with the text and describe the presentation, diagnosis, and management of real patientsfurther clinical material that builds on the basic science and describes the causes of endocrine disorders, their clinical features, and treatment optionscoverage of the latest advances and discoveriesself-assessment questions to test understandingThe book is lavishly illustrated throughout with line drawings and clinical photographs.The authors, one a scientist and the other a clinician, guide you through the complexities of physiology and biochemistry so that you can understand the nature and management of endocrine pathologies. At all times they relate basic science to clinical medicine in a clear and lucid style that is both practical and clinically relevant.From reviews:"Clinical Endocrinology is very well written and beautifully illustrated."Lancet Diabetes Endocrinology, January 2013"All in all this is an excellent, essential textbook which does the job admirably in terms of synthesising the essence of human physiology and excreting a patient-centred approach to addressing the clinical manifestations of endocrine hypo- and hyper-function."The Endocrinologist, December 2013"This book would appeal particularly to medical students or endocrinologists in training... [It] provides a useful review of endocrinology in a comprehensive manner starting from basic science principles and ending with clinical applications."Doody's Notes, May 2013About the authors:Professor Saffron Whitehead is Professor of Endocrine Physiology at St George's Medical School, University of LondonDr John Miell is a Consultant Endocrinologist at University Hospital Lewisham, London

Catch up Biology 2e covers the basic principles and concepts in biology that you will need if you are studying medicine or a related subject, or one of the biomedical sciences. The book focuses on human biology and covers:the basic molecules of life, such as proteins, carbohydrates, nucleic acidscells, tissues and processes, including energy metabolism, cell division, epithelial and connective tissuesthe key mammalian systems, for example, homeostasis, the endocrine, respiratory and digestive systems.Throughout the book the authors highlight clinical examples so that you can see the relevance of basic biology to your course. The book also contains questions (and answers) so that you can test your understanding of the subject as you work through the book. This new edition features two new chapters on microorganisms and on genetic disease. Catch up Biology is the ideal book to refresh your understanding of the basic concepts of biology.

If you are about to study for a degree in the life or medical sciences, you will need to understand some core facts and concepts in chemistry. You do not need to be a budding chemist but you do need to be comfortable with chemical terms and principles.Catch up Chemistry, second edition, will bring you up to speed with the subject and will lay the foundations of chemistry in those topics that will underpin your studies, such as:the nature of atomic structure and molecular bonding the properties of biological molecules and macromoleculesthe gas laws the special properties of waterthermodynamic concepts in biologybiological transport mechanisms and transporters understanding reaction mechanisms and kineticsderiving energy from molecules At every stage the authors remind you of the relevance of this chemistry to your life or medical sciences course - this is not just chemistry for the sake of it. The book also contains a lot of questions (and answers), so that you can test your understanding at any time - it really does get easier with practice!

Catch Up Maths & Stats covers the core maths skills you will need on any life or medical sciences course including: working with fractions and powerspreparation of a dilution serieshow to calculate standard deviationusing and understanding graphsanalysing enzyme kineticschoosing the right statistical testOver 200 examples are provided to show the relevance and application of maths and stats to your course. This second edition also now provides further coverage of differentiation and integration alongside nearly 70 more questions and answers to help you test your understanding. Catch Up Maths & Statswill bring you up to speed in the shortest possible time, even if you didn't study maths at advanced level.

How to use CBT within a typical 10 minute consultation Using CBT in General Practice, second edition provides GPs with an overview of the basic principles of CBT and shows how these principles can be applied within a typical 10 minute consultation. The book is written in a user-friendly, interactive and practical style and focuses on realistic ways to make CBT work by helping patients to make positive changes to their lives. Key features of this second edition include:case examples to highlight how the techniques can be applied in practice for patients with particular problems or clinical conditions, such as coping with negative thoughtsproblem-solving sections describe how to manage time constraintsa new consultation model that can be used to implement CBT in general practicedetailed overviews of the major clinical psychological conditions that can be treated using CBT, such as panic, low self-esteem, and insomnia.Using CBT in General Practice uniquely provides the practical advice needed to implement CBT within the time constraints of a busy practice – it is therefore essential reading for all GPs, who must now offer CBT as a treatment option. As this is a practical manual and not just a book of theory, it will also appeal to other professionals involved in the management of patients with psychological problems such as practice nurses, health visitors, community psychiatric nurses, practice counsellors and palliative care doctors.

Anatomy and Physiology in Healthcare focuses on what healthcare students need to know about the biological principles which underpin the practice of healthcare.All healthcare students have to study anatomy and physiology. They often find it a challenging subject and struggle to see how the subject will link to their professional practice.This book is unique in that it integrates clinical cases with the essential biological facts to provide all students with a thorough understanding of how anatomy and physiology can be applied in healthcare.By using clinical cases throughout , the book helps the reader grasp the practical relevance of anatomy and physiology to decision-making and care delivery.The clinical cases have been carefully selected to reflect common conditions encountered in practice today, and the changing patterns of disease and healthcare.Clear high-quality full colour illustrations, links to appropriate web-based content, and self-assessment material make this the perfect, practical textbook for all healthcare students.Review:"This textbook presents anatomy and physiology in a fun and interactive way.... It is divided into 14 chapters and the way the authors have introduced the information gives it a modern twist. For example, instead of titling a chapter 'The reproductive system', it is called 'From one generation to the next'. ..... What works particularly well is the way the authors have used case studies that reflect the reality of the changing patterns of health and disease.... This book provides a good foundation in clinical application and it seeks to link theory to practice."; Nursing Standard, 27 September 2017, volume 32 number 5