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See Latest ArticlesNon-lethal neonatal neuromuscular variant of glycogenosis type IV with novel GBE1 mutations
Muscle & Nerve, 10/20/09
Fernandez C et al. – The authors report a recent case of the severe congenital variant of glycogen storage disease type IV with prolonged survival. The patient was found to be a compound heterozygote for two novel mutations, a missense mutation in exon 5 (p.H188P, c.563A>C) and a severe mutation in intron 5 (c.691+2T>C).
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Transient Ischemic Attack after Tissue Plasminogen Activator: Aborted Stroke or Unnecessary Stroke Therapy
Cerebrovascular Diseases, 11/10/09
Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
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Neurological symptoms in patients with biopsy proven celiac disease
Movement Disorders, 11/03/09
Today in Neuropathy/Myopathy...keeping you current
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Amitriptyline vs. pregabalin in painful diabetic neuropathy: a randomized double blind clinical trial
Diabetic Medicine, 10/01/09
Accuracy of Monofilament Testing to Diagnose Peripheral Neuropathy: A Systematic Review
Annals of Family Medicine, 11/10/09
Distinct subtypes of myelitis in systemic lupus erythematosus
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