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Results: 2
DETECTION OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIESAMONG PATIENTS WITH ACUTE PAINLESS MONONEUROPATHY OR PLEXOPATHY
Authors: PAREYSON D SOLARI A TARONI F BOTTI S FALLICA E SCAIOLI V CIANO C SGHIRLANZONI A
Citation: D. Pareyson et al., DETECTION OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIESAMONG PATIENTS WITH ACUTE PAINLESS MONONEUROPATHY OR PLEXOPATHY, Muscle & nerve, 21(12), 1998, pp. 1686-1691
VERY MILD CHARCOT-MARIE-TOOTH-DISEASE IN PATIENTS HETEROZYGOUS FOR A LOSS-OF-FUNCTION MUTATION IN THE P-0 GENE
Authors: PAREYSON D MENICHELLA D BOTTI S SGHIRLANZONI A FALLICA E MORA M CIANO C SHY ME TARONI F
Citation: D. Pareyson et al., VERY MILD CHARCOT-MARIE-TOOTH-DISEASE IN PATIENTS HETEROZYGOUS FOR A LOSS-OF-FUNCTION MUTATION IN THE P-0 GENE, Neurology, 50(4), 1998, pp. 8003-8003
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