Bashar Katirji – författare

Continuing the unique case-based learning approach to fill the gap between theory and practice, the third edition of Electromyography in Clinical Practice addresses the advances in neuromuscular medicine, including anterior horn cell disorders, peripheral neuropathies, neuromuscular junction disorders, and myopathies. It is the perfect resource for neurologists, physiatrists, neurosurgeons, orthopedic surgeons, rheumatologists, physical therapists, and pain management specialists, neuromuscular and clinical neurophysiology fellows, as well as the resident, trainee, and medical student interested in the diagnosis and management of the most common disorders encountered in the EMG lab.The book is divided into two major parts; the first an introduction to clinical electromyography and the second is separated into 27 case studies. The cases focus on localized disorders in the lower and upper extremities and end with a selection of generalized disorders. Each case begins with a detailed, tabulated, EMG study, followed by several questions, and a detailed analysis of the study, then takes into account patient history, the physical examination, EMG Neurologists, physiatrists (Physical Medicine andrpen the rehabilitation), Trainees (Neurology and Physical Medicine

Electromyography in Clinical Practice, now in its fourth edition, provides case-based learning of clinical Electromyography (EMG) with a main mission of reducing the gap between theory and practice in the fields of electrodiagnostic (EDX) and neuromuscular medicine. The book format includes four detailed introductory chapters that acquaint the discipline and scope of the EDX Examination. This includes chapters on nerve conduction studies (NCS), needle EMG, specialized EDX testing, and EDX findings in neuromuscular disorders. The second part of the book includes comprehensive presentations of 36 cases that encompass the most common disorders encountered in the EMG laboratory and are presented in a similar layout. These are classified into focal disorders of the lower and upper extremities, cranial nerve disorders and generalized neuromuscular disorders. The book focuses on problem solving through analysis of the data obtained on NCS and needle EMG. This is meant to mimic a bedside analysis of data, like what occurs regularly in the EMG laboratory. The exact values obtained on NCS and specialized tests, and findings on needle EMG are analysed in detail. A differential and final diagnoses are then made. This is followed by a comprehensive discussion of the clinical and EDX findings of the disorder.This text is an ideal book for physicians interested in learning and mastering the clinical practice of clinical EMG. This includes mostly specialists in the fields of neuromuscular medicine, neurology, and physical medicine and rehabilitation, but also include orthopedists, hand surgeons, neurosurgeons, spine surgeons, rheumatologist and pain management specialists.

The only case-based guide to electromyography-back in a fully revised and updated New Edition! This practical resource examines how to approach, diagnose, and manage the most commonly encoun-tered disorders in the EMG laboratory. Based on actual cases, it correlates patient history, physical exam, EMG findings, relevant anatomy, treatment, and follow-up to help readers sharpen their clinical problem-solving skills. New cases have been added, and every case includes the latest advances in knowledge and technique.

The only review book currently available in this complex field, Neuromuscular and Electrodiagnostic Medicine Board Review is an all-in-one, must-have resource for preparing for the neuromuscular and electrodiagnostic medicine, neurology, clinical neurophysiology and physical medicine and rehabilitation board exams. Focused, high-yield content is provided in a concise, readable manner without exhaustive or unnecessary detail, helping you make the most of your study time and efficiently prepare for exams and clinical practice.

Comprehensive, thoroughly updated, and expanded, Neuromuscular Disorders in Clinical Practice, Second Edition encompasses all disorders of the peripheral nervous system, covering all aspects of neuromuscular diseases from diagnosis to treatment.  Mirroring the first book, this two-volume edition is divided into two parts.  Part one discusses the approach to neuromuscular disorders, covering principles and basics, neuromuscular investigations, and assessment and treatment of neurological disorders.  Part two then addresses the complete range of specific neuromuscular diseases: neuronopathies, peripheral neuropathies, neuromuscular junction disorders, muscle ion channel disorders, myopathies, and miscellaneous neuromuscular disorders and syndromes.  Neuromuscular Disorders in Clinical Practice, Second Edition is intended to serve as a comprehensive text for both novice and experienced practitioners.  General neurologists as well as specialists in neuromuscular medicine andtrainees in neuromuscular medicine, clinical neurophysiology and electromyography should find this book inclusive, comprehensive, practical and highly clinically focused.  Additionally, specialists in physical medicine and rehabilitation, rheumatology, neurosurgery, and orthopedics will find the book of great value in their practice.

Comprehensive, thoroughly updated, and expanded, Neuromuscular Disorders in Clinical Practice, Second Edition encompasses all disorders of the peripheral nervous system, covering all aspects of neuromuscular diseases from diagnosis to treatment.

This comprehensive title covers all of the broad aspects of stiff-person spectrum disorders (SPSD), ranging from clinical features and laboratory investigations to the basic scientific roles of neuroimmunology and genetics that aid clinicians in understanding the pathogenesis of this disorder.Organized across 15 chapters, this highly practical book begins with a thorough account of the history and clinical phenomenology of SPSD.  Subsequent chapters then delve into the differential diagnoses of the disorder, as well as its electrophysiology, immunopathogenesis, and neurochemistry. Following this is an analysis of each subtype of SPSD including classic stiff-person syndrome and its variants, correlations between clinical phenotypes and antibodies, as well as SPSD in the pediatric population. Finally, the book concludes with an examination of the various SPSD diagnostic approaches, treatments, and potential emergencies seen in clinical practice.Developed by a renowned multidisciplinary authorship, Stiff-Person Syndrome and Related Disorders is an indispensable contribution to the clinical literature and will be of great interest to both clinicians and basic science researchers.