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.