NEUROMUSCULAR DISEASE CENTER  

Washington University School of Medicine, St. Louis, MO

Overview, Search, Index, Links, Pathology, Molecules, Syndromes, New
Muscle, NMJ, Nerve, Spinal, Ataxia, Antibody & Biopsy, Patient Info



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Limb Girdle MDImmune MyopathiesNMJ DisordersMotor Neuron DisordersMyopathy + AntibodiesNerve DDxDemyelinating PNImmune Axonal NeuropathiesMuscle ProteinsMyelin ProteinsAxon TypesDystrophinopathiesMitochondrial DisordersCMTCIDPMuscle DDx


SEARCH: Neuromuscular


  Neuromuscular Fellowship
    July 2002

 
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  New or Revised Pages
 
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DISORDERS & SYNDROMES
Myopathy   Neuropathy      
NM Junction   Motor Neuron
Spinal cord   Cerebellar
SYNDROMES:   Neuromuscular; CNS
 
INDEXES
Alphabetical index  

Texts
On-line
Search Neuromuscular
Molecular & Cellular
Pathology & Illustrations
Laboratory testing: Antibodies
 
NEUROMUSCULAR EVALUATION
General principles
Outline for
residents & students
Disease patterns: Wallet WebSites
Evaluations: Clinical; Laboratory
 
ANTIBODY TESTING
GM1 ganglioside    Sulfatide MAG
GALOP Hu Decorin (BJ)   Other
Neuromuscular Clinical Laboratory
 
NEUROMUSCULAR DIVISION
Personnel and Overview      
Working late
Clinical Laboratory
Biopsies: Muscle & Nerve
Neurology: Directory
School of Medicine
BJC Health System
 

LINKS

  External
 
  Patient information
 
  Links in text
    OMIM Inheritance in Man (OMIM)
    Expasy SWISS-PROT: Proteins


 
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Alan Pestronk, MD
WebSite Author
Send comments to:
pestronk@kids.wustl.edu


ALSO SEE:
    Neurology Department
    DISCLAIMER! & Praise
    Evaluation form




NEW or REVISED

June
B12 deficiency
Churg-Strauss
MG: Ocular
SPG 17 (Silver syndrome)
May
Ataxia: CoQ10 deficiency
b-Enolase
Bulbo-spinal muscular atrophy
Cardiomyopathy
  CMH6
  Hypertrophic
CIDP: Variants
Distal motor axons
EMG: Partial denervation
Goldberg-Shprintzen
HMG CoA synthase deficiency
HNPP
Hypo-K+ periodic paralysis
K+ channels: KCNJ2
Macrophagic myofasciitis
MAG neuropathy
Migrant sensory neuritis
Muscle-Eye-Brain disorders
Muscles: Focal enlargement
Myopathy + Excess autophagy
Neuralgic amyotrophy
Neuroacanthocytosis
Periodic paralysis
  Andersen syndrome
  Comparative features
POEMS syndrome
Neuropathy + Respiratory failure
  Lethal neonatal axonal
  Infantile axonal
Rod myopathy: Pathology
Receptors
  Adenosine
  ATP
  Purine (P2)
Sensory neuronopathy: Anti-Hu
SPG15
Tangier disease
VLCAD, myopathic type
April
Adrenomyeloneuropathy
Ataxia + Intellectual deterioration
Cl- channels: Disorders
Congenital MD + rigid spine
Connective tissue disease
  Scleroderma
  Vasculitis
Episodic ataxia 2
Erythromelalgia
Ethylene glycol
Motor neuron Disorders
  Differential Diagnosis
  Distal HMN 7
HIBM + Respiratory failure
Immunomodulation
  Treatment strategies
LGMD 2A
Miller Fisher syndrome
Multifocal motor neuropathy
Neuralgic amyotrophy
POEMS syndrome
Potassium channels: KCNK type
Scapular winging
Search
SPG2
Sports & Occupations
Strychnine
Tomaculae
Wallerian degeneration

l 1996-2001 Revisions


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