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pro vyhledávání: '"Alexandra, J. -F."'
Autor:
Lidove, O., Chauveheid, M.-P., Caillaud, C., Froissart, R., Benoist, L., Alamowitch, S., Doan, S., Szalat, R., Baumann, N., Alexandra, J.-F., Lavallée, P., Klein, I., Vuillemet, F., Sedel, F., Sacré, K., Samson, Y., Roullet, E., Papo, T.
Publikováno v:
International Journal of Clinical Practice
International Journal of Clinical Practice, 2009, 63 (11), pp.1663-7. ⟨10.1111/j.1742-1241.2009.02115.x⟩
International Journal of Clinical Practice, Wiley, 2009, 63 (11), pp.1663-7. ⟨10.1111/j.1742-1241.2009.02115.x⟩
International Journal of Clinical Practice, 2009, 63 (11), pp.1663-7. ⟨10.1111/j.1742-1241.2009.02115.x⟩
International Journal of Clinical Practice, Wiley, 2009, 63 (11), pp.1663-7. ⟨10.1111/j.1742-1241.2009.02115.x⟩
International audience; BACKGROUND: Fabry disease (OMIM 301 500) is an X-linked lysosomal storage disease. Neurological symptoms in Fabry disease mainly include stroke, acroparesthesia, cranial nerve palsies and autonomic dysfunction. We report on as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2f484f81e013e7afba24f9e74fc3e904
https://inria.hal.science/hal-00805397
https://inria.hal.science/hal-00805397