DIT arquivo atualizado em dez 2012 para ebook definitivo

Chapter 1 		Neuromuscular Anatomy and FunctionChapter 2		Neurological Evaluation and Ancillary TestsChapter 3		Therapy in Neuromuscular DiseasesCase 1	Carpal Tunnel Syndrome in an Elderly Woman Likely from Rheumatoid Arthritis and the Use of a WalkerCase 2	A Uremic Patient with a Shunt-Related Ischemic Monomelic Neuropathy Later Diagnosed with Carpal Tunnel Syndrome from Beta-2 Microglobulin AccumulationCase 3	A Diabetic with Peripheral Neuropathy and Carpal Tunnel Syndrome Who Later Developed DysautonomiaCase 4		Martin Gruber and Anastomosis and Carpal Tunnel SyndromeCase 5	Traumatic Median Neuropathy at the Elbow Mimicking Anterior Interossei SyndromeCase 6		Pronator Teres SyndromeCase 7		Ulnar Entrapment at the ElbowCase 8		Ulnar Neuropathy at the Wrist from a Ganglion CystCase 9		Focal Myositis Causing Radial NeuropathyCase 10	Musculoskeletal Neuropathy from Compression During Positioning for Back SurgeryCase 11	Acute Brachial NeuritisCase 12	Lower Trunk Plexopathy and Horner's Syndrome from LymphomaCase 13 	Radiation PlexopathyCase 14	Suprascapular NeuropathyCase 15	C6 Radiculopathy with Motor Deficits from Herpes Zoster			Case 16	C5 Radiculopathy from a Ruptured DiscCase 17	C7 Radiculopathy from a Herniated DiscCase 18	L4 Radiculopathy from a Disc Herniation and Peroneal EntrapmentCase 19	S1 RadiculopathyCase 20	L5 Radiculopathy and an Accessory Peroneal NerveCase 21	L2 Radiculopathy from Tumor InvasionCase 22	Demylinating Lumbosacral Radiculoneuropathy in a DiabeticCase 23	Cauda Equina Syndrome from Spinal StenosisCase 24	Sciatic Neurofibroma Mimicking Tarsal Tunnel SyndromeCase 25	Femoral Neuropathy from a Hematoma from AngiographyCase 26	Carcinomatous Lumbosacral PlexopathyCase 27	Meralgia ParestheticaCase 28	Lumbosacral Ependymoma Mimicking a Motor Neuron DiseaseCase 29	Acute Facial NeuropathyCase 30	Neurosarcoidosis Presenting with Bilateral Vi and Vii Nerve PalsiesCase 31	A Patient with Als Presenting with Head DropCase 32	Man in the Barrel SyndromeCase 33	Benign Focal Amyotrophy or Monomelic AmyotrophyCase 34	Post-Myelopathy AmyotrophyCase 35	Tethered Cord Syndrome Causing Muscle Pseudohypertrophy from Partial DenervationCase 36	Kennedy's DiseaseCase 37	Machado-Joseph DiseaseCase 38	Infantile Spinal Muscular AtrophyCase 39	Guillain Barre Syndrome with Central DemyelinationCase 40	Acute Inflammatory Polyneuropathy in an HIV Positive PersonCase 41	Miller Fisher SyndromeCase 42	Ciguatera PoisoningCase 43	Acute Quadriplegic Polyneuropathy from PorphyriaCase 44	Critical Illness MyopathyCase 45	Pernicious Anemia Presenting with Hand Numbness in a Patient with Cervical SpondylosisCase 46	Pernicious Anemia Manifesting with Weakness and Abnormal GaitCase 47	Chronic Inflammatory Demyelinating PolyneuropathyCase 48	Chronic Inflammatory Demyelinating Polyneuropathy withAsymmetric Presentation in a Patient with a Monoclonal Gammopathy Case 49	Purely Motor Chronic Inflammatory Demyelinating PolyneuropathyCase 50	Subacute Inflammatory Demyelinating Polyneuropathy in a DiabeticCase 51	Demyelinating Neuropathy Associated with MAG AntibodiesCase 52	Hereditary Demyelinating Polyneuropathy with Multiple SclerosisCase 53	Inflammatory Polyneuropathy after Bariatric SurgeryCase 54	Diabetic AmyotrophyCase 55	Diabetic Amyotrophy/Mononeuritis Multiplex in the Upper ExtremitiesCase 56	Diabetic Muscle InfarctCase 57	Uremic NeuropathyCase 58	(A) Demyelinating Charcot-Marie-Tooth Disease (B) Axonal Charcot-Marie-Tooth DiseaseCase 59	Hereditary Polyneuropathy with Liability to Pressure Palsy Presenting with Bilateral Median Neuropathy after Snow SkiingCase 60	Hereditary Neuropathy with Liability to Pressure Palsy Presenting with a FootdropCase 61	Mononeuritis Multiplex from Vasculitic NeuropathyCase 62	Vasculitic Neuropathy from Rheumatoid ArthritisCase 63	Wegener's Granulomatosis and Peripheral NeuropathyCase 64	Neurolymphomatosis Presenting with Mononeuritis MultiplexCase 65	Paraneoplastic GanglioneuritisCase 66	Familial Amyloid NeuropathyCase 67	Amiodarone NeuropathyCase 68	Myasthenia Gravis Presenting with Difficulty SwallowingCase 69	Familial Myasthenia Gravis with Recurrence after ThymectomyCase 70	Eaton Lambert Myasthenic Syndrome Secondary to Small Cell Carcinoma of the LungCase 71	Eaton Lambert Myasthenic Syndrome in a Patient with Hypothyroidism and Later Uterine CarcinomaCase 72	Slow Channel Congenital Myasthenic SyndromeCase 73	Hypokalemic Periodic ParalysisCase 73	Thyrotoxic Periodic ParalysisCase 74	Becker's Muscular Dystrophy Presenting with Large MusclesCase 75	A Manifest Carrier of Muscular DystrophyCase 76	Distal Muscular Dystrophy from Dysferlin DeficiencyCase 77	Oculopharyngeal Muscular DystrophyCase 78	Facioscapulohumeral Muscular DystrophyCase 79	Merosin Deficient Congenital Muscular DystrophyCase 80	Central Core Disease Manifesting with Progressive Weakness in an AdultCase 81	Mitochondrial Disease Manifests as Progressive External Ophthalmoplegia Mimicking Myasthenia GravisCase 82	Mitochondrial Myopathy with Prominent Neck LipomaCase 83	Rhabdomyolysis in a Patient with Myophosphorylase DeficiencyCase 84	Adult Onset Acid Maltase DeficiencyCase 85	Myoglobinuria from a Viral Infection as the First Manifestation of Carnitine Palmitoyltransferase (Cpt) Deficiency in An AdultCase 86	Proximal Weakness from Beta-2 Microglobulin Accumulation in a Uremic PatientCase 87	Hypothyroid MyopathyCase 88	Hypoparathyroid MyopathyCase 89	Dermatomyositis in a Mother and Her SonCase 90	Polymyositis and Myoadenylate Deaminase Deficiency (Double Trouble?)Case 91	Inclusion Body MyositisCase 92	Inclusion Body Myositis in a Young HIV Positive PersonCase 93	Eosinophilic FascitisCase 94	Bent Spine SyndromeCase 95	A Case of Stiff Person Syndrome and Myasthenia GravisCase 96	Cramp Fasciculation Syndrome from a Chronic, Predominantly Motor NeuronopathyCase 97	Myotonic CongenitaCase 98	Schwartz-Jampel SyndromeCase 99	TetanyCase 100	Proximal Myotonic MyopathyCase 101 	Acquired Rippling Muscle Disease