NEUROMUSCULAR DISEASE CENTER   Washington University School of Medicine, St. Louis, MO
	or Revised Active clinical trials External links Patient information Reference Links Biochemistry topics Inheritance in Man (OMIM) Search ; New Swiss protein data base Swiss enzyme data base MEDLINE M	Neuromuscular, Spinal & Cerebellar Disorders and Syndromes: Disorders: History, Exam, & Lab Myopathy | NM Junction Polyneuropathy | Motor Neuron CNS: Spinal Cord | Cerebellar Syndromes: Neuromuscular | CNS Molecular & Cellular classifications Pathology & Illustrations INDEX: Alphabetical SEARCH: The Neurology Website Neuromuscular Evaluation: Guides History & Examination Laboratory testing Neuromuscular Disease: Patterns Wallet WebSites Autoantibody Testing: Guidelines GM1 ganglioside | Sulfatide | MAG GALOP | Hu | Decorin (BJ) | Other Neuromuscular Clinical Laboratory Neuromuscular Division Personnel and Overview Clinical Laboratory

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WebSite Author: Alan Pestronk, MD Send comments and ideas for revisions or new topics to: pestronk@kids.wustl.edu

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January Amyloidoma Ataxia: Dominant Bulbo-Spinal Muscular Atrophy Carpal tunnel syndrome: Childhood CMT & deafness (Recessive) Congenital myopathy: Mitochondrial Structure Cranial nerve anatomy 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 DNA repeat disorders FK506 (Tacrolimus) Hopkins' syndrome K+ channels: KCNQ type Myasthenia gravis: Associated disorders Myopathies with tubular aggregates Oculopharyngeal muscular dystrophy

December Absent muscles: Holt-Oram B12 deficiency CMT2 Emery-Dreifuss muscular dystrophy Inflammatory & immune myopathies Anti-decorin (BJ antigen) Focal myositis Graft-vs-Host disease Granulomas: Etiology Mitochondrial disorders Myasthenia Gravis: Immune; Clinical Pathology Neonatal perifascicular myopathy Refsum's syndromes Wallet WebSite: Myopathy 1996-1997 Revisions

November ALS: Recessive syndromes AP Ca++ channels: P-type & SCA6 Desmin storage myopathies DNA repeat sequences: CAG Epidural lipomatosis Geniospasm Illustrations & Pathology Becker muscular dystrophy Denervation: Ongoing Dermatomyositis Glycogen metabolic pathways Inflammation: Cell patterns Inflammatory myopathy Lipid storage Muscle fiber structure & contraction Myotonic dystrophy Phosphorylase deficiency Inflammatory & immune myopathies Ion channels Diagrams K+ channels & disorders Na+ channels & disorders Multicore disease Thermosensitive neuropathy Tick paralysis Ubiquitin & Protein degradation