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MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2
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Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia
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CasprI/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.
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INTERMEDIATE SYNDROME DUE TO PROLONGED PARATHION POISONING.
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BECKER-TYPE MUSCULAR-DYSTROPHY - REPORT OF A FAMILY WITH ONE POSTMORTEM STUDY.
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Dermatomyositis with paracrystalline inclusions and polymicrogyria in two sisters
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Polymicrogyria and dermatomyositis in two sisters