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Revue Neurologique|November 7, 2006
[The diagnosis and management of familial amyloid polyneuropathy]V Planté-BordeneuveHandbook of Clinical Neurology|August 13, 2013
Transthyretin familial amyloid polyneuropathyV Planté-Bordeneuve, P KerschenCurrent Opinion in Neurology|November 10, 2000
Transthyretin related familial amyloid polyneuropathyV Planté-Bordeneuve, G SaidPresse Medicale (Paris, France : 1983)|March 1, 1997
[Atypical familial parkinsonian syndromes. Parkinson diseases or specific entities?]D Taussig, V Planté-BordeneuveJournal of the Neurological Sciences|November 1, 1995
A clinical and genetic study of familial cases of Parkinson's diseaseV Planté-Bordeneuve, D Taussig, F Thomas, et al.Annals of Neurology|April 22, 1999
Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas diseaseY Parman, V Planté-Bordeneuve, A Guiochon-Mantel, et al.Annals of Neurology|November 30, 1999
The Roussy-Lévy family: from the original description to the geneV Planté-Bordeneuve, A Guiochon-Mantel, C Lacroix, et al.Clinical Genetics|November 21, 2008
Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patientsM Olsson, U Hellman, V Planté-Bordeneuve, et al.Neurology|August 19, 2007
Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP)V Planté-Bordeneuve, A Ferreira, T Lalu, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994
Debrisoquine hydroxylase gene polymorphism in familial Parkinson's diseaseV Planté-Bordeneuve, M B Davis, D M Maraganore, et al.Pageof 3