Planté-Bordeneuve V - Search Results

1

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.

2

Amylo-AFFECT-QOL, a self-reported questionnaire to assess health-related quality of life and to determine the prognosis in cardiac amyloidosis.

Kharoubi M, Bézard M, Broussier A, Galat A, Gounot R, Poullot E, Molinier-Frenkel V, Fanen P, Funalot B, Itti E, Lemonnier F, Sing Chadha GD, Guendouz S, Mallet S, Zaroui A, Audard V, Audureau E, Le Corvoisier P, Hittinger L, Planté Bordeneuve V, Lefaucheur JP, Amiot A, Bequignon E, Bartier S, Leroy V, Teiger E, Oghina S, Damy T. Kharoubi M, et al. Front Cardiovasc Med. 2023 Mar 14;10:1124660. doi: 10.3389/fcvm.2023.1124660. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 36998975 Free PMC article.

3

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

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

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

127 results

Search Page

Filters