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Neuromuscular disordersa comprehensi...

Khadilkar, Satish V.

Neuromuscular disordersa comprehensive review with illustrative cases /

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Neuromuscular disordersby Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel.
其他題名:	a comprehensive review with illustrative cases /
作者:	Khadilkar, Satish V.
其他作者:	Yadav, Rakhil S.
出版者:	Singapore :Springer Singapore :2018.
面頁冊數:	xxxii, 534 p. :ill., digital ;24 cm.
Contained By:	Springer eBooks
標題:	Neuromuscular diseases.
電子資源:	http://dx.doi.org/10.1007/978-981-10-5361-0
ISBN:	9789811053610$q(electronic bk.)

Neuromuscular disordersa comprehensive review with illustrative cases /
Khadilkar, Satish V.

Neuromuscular disordersa comprehensive review with illustrative cases /[electronic resource] :by Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel. - Singapore :Springer Singapore :2018. - xxxii, 534 p. :ill., digital ;24 cm.

Neuromuscular Disorders: A clinical Approach -- Part I: Asymmetric motor weakness -- Motor Neuron Diseases [ALS] -- Hirayama disease and other focal amyotrophies -- Multifocal motor neuropathy -- Acute motor axonal neuropathy -- Facioscapulohumeral muscular dystrophy -- Progressive muscular atrophy -- Post-polio syndrome -- Part II: Symmetric proximal weakness -- Duchenne and Becker muscular dystrophies -- Spinal Muscular atrophy [SMA] -- Idiopathic Inflammatory myopathies -- Limb Girdle muscular Dystrophies [LGMDs] -- Congenital Myasthenic syndromes [CMS] -- Congenital muscular dystrophies -- Congenital myopathies -- Emery Dreifuss Muscular dystrophy -- Oculopharyngeal muscular dystrophy -- Part III: Symmetric distal weakness -- Myotonic dystrophies [DM] -- Distal myopathies -- Distal hereditary motor neuropathies -- Brown Vieletto Van Laere Syndrome -- Part IV: Fluctuating weakness -- Myasthenia Gravis [MG] -- Lambert Eaton Myasthenic Syndrome -- Periodic paralysis -- Part V: Exercise intolerance, muscle stiffness, cramps and contractures -- Metabolic myopathies -- Peripheral nerve hyperexcitability syndromes -- Non dystrophic myotonias -- Part VI: Asymmetric sensory motor weakness -- Individual neuropathies -- Vasculitic neuropathy -- Multifocal acquired demyelinating sensory and motor neuropathy -- Brachial plexopathies -- Lumbosacral plexopathies -- Compressive Radiculopathies -- Leprosy -- Hereditary neuropathy with pressure palsy -- Part VII: Symmetric sensory motor weakness -- Guillain-Barre syndrome -- Charcot-Marie-Tooth disease[CMT] -- Chronic Inflammatory Demyelinating Polyradiculoneuropathy -- X-linked Charcot Marie Tooth disease -- Other Hereditary neuropathies - 1 -- Other hereditary neuropathies - 2 -- Neuropathies secondary to systemic diseases -- Porphyrias -- Part VIII: Predominant sensory syndromes -- Sensory ganglionopathies -- Distal Acquired Demyelinating Symmetric neuropathy -- Paraproteinemic neuropathies -- Miller Fisher Syndrome.

This book provides a concise overview of the diagnosis and therapy of a wide variety of neuromuscular disorders, in tabulated form and with illustrative cases. Treating neuromuscular disorders calls for a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. Yet to date, there has been no single, compact book that offers all the relevant information related to the management of these disorders. This book fills that gap, presenting the state of the art in the field and addressing practical problems together with their solutions. Each chapter covers disorder characteristics, clinical differentiating points, relevant investigations and their interpretation, available genetic testing, best management approaches and counselling. Illustrative cases provide valuable insights, while extensive tables and illustrations mean that information can be rapidly found.

ISBN: 9789811053610$q(electronic bk.)

Standard No.: 10.1007/978-981-10-5361-0doiSubjects--Topical Terms:

281134
Neuromuscular diseases.

LC Class. No.: RC925.5

Dewey Class. No.: 616.744

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505 0 $a Neuromuscular Disorders: A clinical Approach -- Part I: Asymmetric motor weakness -- Motor Neuron Diseases [ALS] -- Hirayama disease and other focal amyotrophies -- Multifocal motor neuropathy -- Acute motor axonal neuropathy -- Facioscapulohumeral muscular dystrophy -- Progressive muscular atrophy -- Post-polio syndrome -- Part II: Symmetric proximal weakness -- Duchenne and Becker muscular dystrophies -- Spinal Muscular atrophy [SMA] -- Idiopathic Inflammatory myopathies -- Limb Girdle muscular Dystrophies [LGMDs] -- Congenital Myasthenic syndromes [CMS] -- Congenital muscular dystrophies -- Congenital myopathies -- Emery Dreifuss Muscular dystrophy -- Oculopharyngeal muscular dystrophy -- Part III: Symmetric distal weakness -- Myotonic dystrophies [DM] -- Distal myopathies -- Distal hereditary motor neuropathies -- Brown Vieletto Van Laere Syndrome -- Part IV: Fluctuating weakness -- Myasthenia Gravis [MG] -- Lambert Eaton Myasthenic Syndrome -- Periodic paralysis -- Part V: Exercise intolerance, muscle stiffness, cramps and contractures -- Metabolic myopathies -- Peripheral nerve hyperexcitability syndromes -- Non dystrophic myotonias -- Part VI: Asymmetric sensory motor weakness -- Individual neuropathies -- Vasculitic neuropathy -- Multifocal acquired demyelinating sensory and motor neuropathy -- Brachial plexopathies -- Lumbosacral plexopathies -- Compressive Radiculopathies -- Leprosy -- Hereditary neuropathy with pressure palsy -- Part VII: Symmetric sensory motor weakness -- Guillain-Barre syndrome -- Charcot-Marie-Tooth disease[CMT] -- Chronic Inflammatory Demyelinating Polyradiculoneuropathy -- X-linked Charcot Marie Tooth disease -- Other Hereditary neuropathies - 1 -- Other hereditary neuropathies - 2 -- Neuropathies secondary to systemic diseases -- Porphyrias -- Part VIII: Predominant sensory syndromes -- Sensory ganglionopathies -- Distal Acquired Demyelinating Symmetric neuropathy -- Paraproteinemic neuropathies -- Miller Fisher Syndrome.
520 $a This book provides a concise overview of the diagnosis and therapy of a wide variety of neuromuscular disorders, in tabulated form and with illustrative cases. Treating neuromuscular disorders calls for a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. Yet to date, there has been no single, compact book that offers all the relevant information related to the management of these disorders. This book fills that gap, presenting the state of the art in the field and addressing practical problems together with their solutions. Each chapter covers disorder characteristics, clinical differentiating points, relevant investigations and their interpretation, available genetic testing, best management approaches and counselling. Illustrative cases provide valuable insights, while extensive tables and illustrations mean that information can be rapidly found.
650 0 $a Neuromuscular diseases. $3 281134
650 0 $a Amyotrophic lateral sclerosis. $3 482141
650 0 $a Duchenne muscular dystrophy. $3 803809
650 0 $a Spinal muscular atrophy. $3 784070
650 1 4 $a Medicine & Public Health. $3 273799
650 2 4 $a Neurology. $3 211583
700 1 $a Yadav, Rakhil S. $3 803807
700 1 $a Patel, Bhagyadhan A. $3 803808
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