NEUROMUSCULAR DISEASE CENTER
Washington University, St. Louis, MO  USA
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DISORDERS & SYNDROMES
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SYNDROMES:   NeuromuscularCNS
 
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NEUROMUSCULAR EVALUATION
General principles
Disease patterns: Wallet WebSites
Evaluations: ClinicalLaboratory
Biopsies: MuscleNerve  
Test forms: NerveMuscle +Antibody

ANTIBODY TESTING
Gangliosides: GM1GalNAc-GD1aGD1bGQ1b
Other: MAGGALOPHuDecorinSulfatide
Neuromuscular Clinical Laboratory: Test form
 
NEUROMUSCULAR DIVISION
OverviewPersonnel
Clinical LaboratoryTrials

New or Revised

April 2005
PEO: Dominant

March 2005
CMT 4A
CMT 4H
Complex regional pain
Cores: Pathology
Danon disease: Pathology
LGMD + Retardation
Marine (channel) toxins
  Brevetoxin
  Domoic acid
  Palytoxin
Multicore
  Pathology
  Syndromes
SPG 28

February 2005
CK High
CMT IA
Fasciitis
  Eosinophilic
  Spanish toxic oil
Gap junctions
Lymphoma
Polymyalgia rheumatica
SCA 26
SPG 6

January 2005
Ataxia + Upgaze palsy
Central hypoventilation
CMT: DIB
Congenital MD
  MDC1C
  Ullrich
Diabetic neuropathy
LGMD 1G
Myofibrillar myopathy
  ZASP
Myotonic dystrophy
  DM1 mechanisms
  DM2
Porphyria
SPG 3A
SPG 26
Tethered cord
Wallet websites
  Printable versions

1996-2005 Revisions

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Alan Pestronk, MD
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pestronka@neuro.wustl.edu
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