Bettina Balint – författare

The neurologic subspecialty of Movement Disorders is complicated with many different entities, making the differential diagnosis difficult. One of the most important aspects of these different entities is their visual appearance. Still photographs do not give sufficient information, but videos like the ones included in this volume can provide dimension, context, and critical information. The variety of visual appearances is wide and seeing many videos is necessary to develop skill in making a diagnosis. Involuntary movements are even more complicated and the adage "seeing is believing" has never been more true. Despite this, few books include videos portraying involuntary movements.Involuntary Movements: Classification and Video Atlas pairs descriptions of the clinical features of various involuntary movements with video depictions of the involuntary movements in action. In a unique approach, this book considers two aspects of the diagnosis of involuntary movements: the phenomenology - as depicted in approximately 200 video supplements - and the etiology. The book also discusses the current consensus on the classification, pathophysiology, and treatment of each involuntary movement.

The Dystonias is a new title introduced under the Contemporary Neurology Series defining the key features of one of the most frequently misdiagnosed of all movement disorders. This volume provides a comprehensive practical clinical resource that addresses how to recognize the many types of dystonia, how they are diagnosed and evaluated, and the currently available medical and surgical treatments. The dystonias are a heterogeneous group of disorders characterized by excessive muscle contractions leading to abnormal postures and movements. The clinical manifestations of dystonias are quite varied. The dystonias may emerge at any age from infancy through late adulthood, they may affect muscles in nearly any region of the body alone or in various combinations, they may occur without other clinical problems, or they may be combined with other neurological or systemic disorders. There are many causes for dystonia too, both acquired and inherited. The chapters explore the clinical manifestations and causes which are quite varied for all age groups. Among adults, the most common syndromes affect a single body region such as the neck (cervical dystonia or torticollis), craniofacial region (blepharospasm or oromandibular dystonia), one limb (writer's cramp or foot dystonia), the larynx (laryngeal dystonia or spasmodic dysphonia), or another region. For adults, most cases are idiopathic, and a cause cannot be found despite extensive workup. For children, dystonia often spreads to involve a broader region of the body, and a cause is more likely to be discovered. The most common syndromes among children include cerebral palsy or genetic disorders where dystonia may occur in isolation or combined with other clinical problems. The Dystonias will be the most useful guide for both pediatric and adult neurologists, as well as specialists in rehabilitation medicine or physiotherapy. This book will also be valuable for neurosurgeons, ophthalmologists, otolaryngologists, developmentalists, rehab specialists and physiotherapists.

The Dystonias is a new title introduced under the Contemporary Neurology Series defining the key features of one of the most frequently misdiagnosed of all movement disorders. This volume provides a comprehensive practical clinical resource that addresses how to recognize the many types of dystonia, how they are diagnosed and evaluated, and the currently available medical and surgical treatments. The dystonias are a heterogeneous group of disorders characterized by excessive muscle contractions leading to abnormal postures and movements. The clinical manifestations of dystonias are quite varied. The dystonias may emerge at any age from infancy through late adulthood, they may affect muscles in nearly any region of the body alone or in various combinations, they may occur without other clinical problems, or they may be combined with other neurological or systemic disorders. There are many causes for dystonia too, both acquired and inherited. The chapters explore the clinical manifestations and causes which are quite varied for all age groups. Among adults, the most common syndromes affect a single body region such as the neck (cervical dystonia or torticollis), craniofacial region (blepharospasm or oromandibular dystonia), one limb (writer's cramp or foot dystonia), the larynx (laryngeal dystonia or spasmodic dysphonia), or another region. For adults, most cases are idiopathic, and a cause cannot be found despite extensive workup. For children, dystonia often spreads to involve a broader region of the body, and a cause is more likely to be discovered. The most common syndromes among children include cerebral palsy or genetic disorders where dystonia may occur in isolation or combined with other clinical problems. The Dystonias will be the most useful guide for both pediatric and adult neurologists, as well as specialists in rehabilitation medicine or physiotherapy. This book will also be valuable for neurosurgeons, ophthalmologists, otolaryngologists, developmentalists, rehab specialists and physiotherapists.

The Dystonias is a new title introduced under the Contemporary Neurology Series defining the key features of one of the most frequently misdiagnosed of all movement disorders. This volume provides a comprehensive practical clinical resource that addresses how to recognize the many types of dystonia, how they are diagnosed and evaluated, and the currently available medical and surgical treatments. The dystonias are a heterogeneous group of disorders characterized by excessive muscle contractions leading to abnormal postures and movements. The clinical manifestations of dystonias are quite varied. The dystonias may emerge at any age from infancy through late adulthood, they may affect muscles in nearly any region of the body alone or in various combinations, they may occur without other clinical problems, or they may be combined with other neurological or systemic disorders. There are many causes for dystonia too, both acquired and inherited. The chapters explore the clinical manifestations and causes which are quite varied for all age groups. Among adults, the most common syndromes affect a single body region such as the neck (cervical dystonia or torticollis), craniofacial region (blepharospasm or oromandibular dystonia), one limb (writer's cramp or foot dystonia), the larynx (laryngeal dystonia or spasmodic dysphonia), or another region. For adults, most cases are idiopathic, and a cause cannot be found despite extensive workup. For children, dystonia often spreads to involve a broader region of the body, and a cause is more likely to be discovered. The most common syndromes among children include cerebral palsy or genetic disorders where dystonia may occur in isolation or combined with other clinical problems. The Dystonias will be the most useful guide for both pediatric and adult neurologists, as well as specialists in rehabilitation medicine or physiotherapy. This book will also be valuable for neurosurgeons, ophthalmologists, otolaryngologists, developmentalists, rehab specialists and physiotherapists.

Experienced neurologists work fast. They take a brief history, perform a short examination (if that), and make an accurate diagnosis. Traditionally such skill stems from experience but diagnostic expertise can be taught. This approach is the core philosophy of Instant Neurological Diagnosis.First published in 2016, Instant Neurological Diagnosis quickly became a must-have for the practicing neurologist looking to acquire the expertise to make rapid diagnoses. This best-selling guide became an indispensable source of diagnostic clues, starting from a patient's appearance all the way down to a directed clinical examination. In this completely revised and updated resource, the authors continue to provide a one-of-a-kind work that illustrates unique neurologic cases with their specific signs and clues, without revealing the actual diagnosis. Reinforced with over 200 videos, every trade secret ('Handle') the authors know is listed in the relevant chapters along with warning messages termed 'Red Flags'. With the aid of these powerful diagnostic shortcuts, the reader is guided rapidly toward the correct conclusion.

Experienced neurologists work fast. They take a brief history, perform a short examination (if that), and make an accurate diagnosis. Traditionally such skill stems from experience but diagnostic expertise can be taught. This approach is the core philosophy of Instant Neurological Diagnosis.First published in 2016, Instant Neurological Diagnosis quickly became a must-have for the practicing neurologist looking to acquire the expertise to make rapid diagnoses. This best-selling guide became an indispensable source of diagnostic clues, starting from a patient's appearance all the way down to a directed clinical examination. In this completely revised and updated resource, the authors continue to provide a one-of-a-kind work that illustrates unique neurologic cases with their specific signs and clues, without revealing the actual diagnosis. Reinforced with over 200 videos, every trade secret ('Handle') the authors know is listed in the relevant chapters along with warning messages termed 'Red Flags'. With the aid of these powerful diagnostic shortcuts, the reader is guided rapidly toward the correct conclusion.