Neuromuscular Disorders A Comprehensive Review with Illustrative Cases /

• Κύριοι συγγραφείς: Khadilkar, Satish V. (Συγγραφέας, http://id.loc.gov/vocabulary/relators/aut), Yadav, Rakhil S. (http://id.loc.gov/vocabulary/relators/aut), Patel, Bhagyadhan A. (http://id.loc.gov/vocabulary/relators/aut)
• Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
• Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
• Γλώσσα: English
• Έκδοση: Singapore : Springer Singapore : Imprint: Springer, 2018.
• Έκδοση: 1st ed. 2018.
• Θέματα: Neurology .; Neurology.

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 investigat...

Πίνακας περιεχομένων:

• 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-Barré 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.