Planté-Bordeneuve V - Search Results

1

Nerve granulomas and vasculitis in sarcoid peripheral neuropathy: a clinicopathological study of 11 patients.

Said G, Lacroix C, Planté-Bordeneuve V, Le Page L, Pico F, Presles O, Senant J, Remy P, Rondepierre P, Mallecourt J. Said G, et al. Brain. 2002 Feb;125(Pt 2):264-75. doi: 10.1093/brain/awf027. Brain. 2002. PMID: 11844727

2

A multicentric study of the disease risks and first manifestations in hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis.

Planté-Bordeneuve V, Gorram F, Olsson M, Anan I, Mazzeo A, Gentile L, Cisneros-Barroso E, Gonzalez-Moreno J, Losada I, Waddington-Cruz M, Pinto LF, Parman Y, Fanen P, Alarcon F, Nuel G. Planté-Bordeneuve V, et al. Amyloid. 2023 Sep;30(3):313-320. doi: 10.1080/13506129.2023.2178891. Epub 2023 Feb 21. Amyloid. 2023. PMID: 36994840

3

Peduncular 'rubral' tremor and dopaminergic denervation: a PET study.

Remy P, de Recondo A, Defer G, Loc'h C, Amarenco P, Planté-Bordeneuve V, Dao-Castellana MH, Bendriem B, Crouzel C, Clanet M, et al. Remy P, et al. Neurology. 1995 Mar;45(3 Pt 1):472-7. doi: 10.1212/wnl.45.3.472. Neurology. 1995. PMID: 7898699

4

A clinical and genetic study of familial cases of Parkinson's disease.

Planté-Bordeneuve V, Taussig D, Thomas F, Ziégler M, Said G. Planté-Bordeneuve V, et al. J Neurol Sci. 1995 Nov;133(1-2):164-72. doi: 10.1016/0022-510x(95)00190-d. J Neurol Sci. 1995. PMID: 8583221 Clinical Trial.

5

Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.

Planté-Bordeneuve V, Taussig D, Thomas F, Said G, Wood NW, Marsden CD, Harding AE. Planté-Bordeneuve V, et al. Neurology. 1997 Jun;48(6):1589-93. doi: 10.1212/wnl.48.6.1589. Neurology. 1997. PMID: 9191771

6

Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathy.

Planté-Bordeneuve V, Lalu T, Misrahi M, Reilly MM, Adams D, Lacroix C, Said G. Planté-Bordeneuve V, et al. Neurology. 1998 Sep;51(3):708-14. doi: 10.1212/wnl.51.3.708. Neurology. 1998. PMID: 9748014

7

Recessive inheritance of a new point mutation of the PMP22 gene in Dejerine-Sottas disease.

Parman Y, Planté-Bordeneuve V, Guiochon-Mantel A, Eraksoy M, Said G. Parman Y, et al. Ann Neurol. 1999 Apr;45(4):518-22. doi: 10.1002/1531-8249(199904)45:4<518::aid-ana15>3.0.co;2-u. Ann Neurol. 1999. PMID: 10211478

8

The Roussy-Lévy family: from the original description to the gene.

Planté-Bordeneuve V, Guiochon-Mantel A, Lacroix C, Lapresle J, Said G. Planté-Bordeneuve V, et al. Ann Neurol. 1999 Nov;46(5):770-3. doi: 10.1002/1531-8249(199911)46:5<770::aid-ana13>3.0.co;2-u. Ann Neurol. 1999. PMID: 10553995

9

Transthyretin related familial amyloid polyneuropathy.

Planté-Bordeneuve V, Said G. Planté-Bordeneuve V, et al. Curr Opin Neurol. 2000 Oct;13(5):569-73. doi: 10.1097/00019052-200010000-00011. Curr Opin Neurol. 2000. PMID: 11073365 Review.

10

The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases.

Planté-Bordeneuve V, Parman Y, Guiochon-Mantel A, Alj Y, Deymeer F, Serdaroglu P, Eraksoy M, Said G. Planté-Bordeneuve V, et al. J Neurol. 2001 Sep;248(9):795-803. doi: 10.1007/s004150170096. J Neurol. 2001. PMID: 11596785

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