Pr Violaine PLANTE-BORDENEUVE

Results: 38

1.
Tafamidis for transthyretin familial amyloid polyneuropathy: A randomized, controlled trial.
Coelho T, Maia LF, Martins da Silva A, Waddington Cruz M, Planté-Bordeneuve V, Lozeron P, Suhr OB, Campistol JM, Conceição IM, Schmidt HH, Trigo P, Kelly JW, Labaudinière R, Chan J, Packman J, Wilson A, Grogan DR.
Neurology
. 2012 Aug 21;79(8):785-92. Epub 2012 Jul 25.
PMID: 22843282
[PubMed - in process]
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2.
A brief compound test for assessment of autonomic and sensory-motor dysfunction in familial amyloid polyneuropathy.
Denier C, Ducot B, Husson H, Lozeron P, Adams D, Meyer L, Said G, Planté-Bordeneuve V.
J Neurol
. 2007 Dec;254(12):1684-8. Epub 2007 Dec 14.
PMID: 18074076
[PubMed - indexed for MEDLINE]
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3.
Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients.
Olsson M, Hellman U, Planté-Bordeneuve V, Jonasson J, Lång K, Suhr OB.
Clin Genet
. 2009 Feb;75(2):163-8. Epub 2008 Nov 1.
PMID: 19018796
[PubMed - indexed for MEDLINE]
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4.
On the origin of the transthyretin Val30Met familial amyloid polyneuropathy.
Zaros C, Genin E, Hellman U, Saporta MA, Languille L, Wadington-Cruz M, Suhr O, Misrahi M, Planté-Bordeneuve V.
Ann Hum Genet
. 2008 Jul;72(Pt 4):478-84. Epub 2008 May 5.
PMID: 18460047
[PubMed - indexed for MEDLINE]
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5.
Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population.
Hellman U, Alarcon F, Lundgren HE, Suhr OB, Bonaiti-Pellié C, Planté-Bordeneuve V.
Amyloid
. 2008 Sep;15(3):181-6.
PMID: 18925456
[PubMed - indexed for MEDLINE]
Free PMC Article
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6.
TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?
Bonaïti B, Olsson M, Hellman U, Suhr O, Bonaïti-Pellié C, Planté-Bordeneuve V.
Eur J Hum Genet. 2010 Aug;18(8):948-52. Epub 2010 Mar 17.
PMID: 20234390
[PubMed - indexed for MEDLINE]
Free PMC Article
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7.
A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers.
Olsson M, Norgren N, Obayashi K, Plante-Bordeneuve V, Suhr OB, Cederquist K, Jonasson J.
BMC Med Genet
. 2010 Sep 14;11:130.
PMID: 20840742
[PubMed - indexed for MEDLINE]
Free PMC Article
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8.
PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history.
Alarcon F, Bourgain C, Gauthier-Villars M, Planté-Bordeneuve V, Stoppa-Lyonnet D, Bonaïti-Pellié C.
Genet Epidemiol
. 2009 Jul;33(5):379-85.
PMID: 19089844
[PubMed - indexed for MEDLINE]
Free PMC Article
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9.
Familial amyloid polyneuropathy.
Planté-Bordeneuve V, Said G.
Lancet Neurol. 2011 Dec;10(12):1086-97. Review.
PMID: 22094129
[PubMed - indexed for MEDLINE]
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10.
Transthyretin related familial amyloid polyneuropathy.
Planté-Bordeneuve V, Said G.
Curr Opin Neurol
. 2000 Oct;13(5):569-73. Review.
PMID: 11073365
[PubMed - indexed for MEDLINE]
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11.
Penetrance estimation of TTR familial amyloid polyneuropathy (type I) in Brazilian families.
Saporta MA, Zaros C, Cruz MW, André C, Misrahi M, Bonaïti-Pellié C, Planté-Bordeneuve V.
Eur J Neurol. 2009 Mar;16(3):337-41.
PMID: 19364362
[PubMed - indexed for MEDLINE]
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12.
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.
Neurology
. 1998 Sep;51(3):708-14.
PMID: 9748014
[PubMed - indexed for MEDLINE]
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13.
Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP).
Planté-Bordeneuve V, Ferreira A, Lalu T, Zaros C, Lacroix C, Adams D, Said G.
Neurology
. 2007 Aug 14;69(7):693-8.
PMID: 17698792
[PubMed - indexed for MEDLINE]
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14.
Discordant expression of familial amyloid polyneuropathy in monozygotic Brazilian twins.
Saporta MA, Plante-Bordeneuve V, Misrahi M, Cruz MW.
Amyloid. 2009 Mar;16(1):38-41.
PMID: 19291513
[PubMed - indexed for MEDLINE]
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15.
A clinical and genetic study of familial cases of Parkinson's disease.
Planté-Bordeneuve V, Taussig D, Thomas F, Ziégler M, Said G.
J Neurol Sci
. 1995 Nov;133(1-2):164-72.
PMID: 8583221
[PubMed - indexed for MEDLINE]
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16.
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.
Brain. 2002 Feb;125(Pt 2):264-75.
PMID: 11844727
[PubMed - indexed for MEDLINE]
Free Article
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17.
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.
J Neurol
. 2001 Sep;248(9):795-803.
PMID: 11596785
[PubMed - indexed for MEDLINE]
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18.
Clinicopathological aspects of the neuropathy of neurogastrointestinal encephalomyopathy (MNGIE) in four patients including two with a Charcot-Marie-Tooth presentation.
Said G, Lacroix C, Planté-Bordeneuve V, Messing B, Slama A, Crenn P, Nivelon-Chevallier A, Bedenne L, Soichot P, Manceau E, Rigaud D, Guiochon-Mantel A, Matuchansky C.
J Neurol
. 2005 Jun;252(6):655-62. Epub 2005 Mar 7.
PMID: 15742109
[PubMed - indexed for MEDLINE]
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19.
Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.
Plante-Bordeneuve V, Said G.
Muscle Nerve
. 2002 Nov;26(5):608-21. Review.
PMID: 12402282
[PubMed - indexed for MEDLINE]
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20.
Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndrome.
Slama A, Lacroix C, Plante-Bordeneuve V, Lombès A, Conti M, Reimund JM, Auxenfants E, Crenn P, Laforêt P, Joannard A, Seguy D, Pillant H, Joly P, Haut S, Messing B, Said G, Legrand A, Guiochon-Mantel A.
Mol Genet Metab
. 2005 Apr;84(4):326-31. Epub 2005 Jan 24.
PMID: 15781193
[PubMed - indexed for MEDLINE]
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21.
The Roussy-Lévy family: from the original description to the gene.
Planté-Bordeneuve V, Guiochon-Mantel A, Lacroix C, Lapresle J, Said G.
Ann Neurol. 1999 Nov;46(5):770-3.
PMID: 10553995
[PubMed - indexed for MEDLINE]
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22.
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.
Neurology
. 1997 Jun;48(6):1589-93.
PMID: 9191771
[PubMed - indexed for MEDLINE]
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23.
[Atypical familial parkinsonian syndromes. Parkinson diseases or specific entities?].
Taussig D, Planté-Bordeneuve V.
Presse Med
. 1997 Mar 1;26(6):290-6. Review. French.
PMID: 9122134
[PubMed - indexed for MEDLINE]
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24.
Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.
Planté-Bordeneuve V, Davis MB, Maraganore DM, Marsden CD, Harding AE.
J Neurol Neurosurg Psychiatry
. 1994 Aug;57(8):911-3.
PMID: 8057112
[PubMed - indexed for MEDLINE]
Free PMC Article
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25.
Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease.
Planté-Bordeneuve V, Davis MB, Maraganore DM, Marsden CD, Harding AE.
Mov Disord
. 1994 May;9(3):337-9.
PMID: 7913740
[PubMed - indexed for MEDLINE]
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26.
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.
Ann Neurol
. 1999 Apr;45(4):518-22.
PMID: 10211478
[PubMed - indexed for MEDLINE]
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27.
CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.
Planté-Bordeneuve V, Bandmann O, Wenning G, Quinn NP, Daniel SE, Harding AE.
Mov Disord
. 1995 May;10(3):277-8.
PMID: 7651442
[PubMed - indexed for MEDLINE]
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28.
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.
Neurology. 1995 Mar;45(3 Pt 1):472-7.
PMID: 7898699
[PubMed - indexed for MEDLINE]
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29.
Impact of liver transplantation on cardiac autonomic denervation in familial amyloid polyneuropathy.
Delahaye N, Rouzet F, Sarda L, Tamas C, Dinanian S, Plante-Bordeneuve V, Adams D, Samuel D, Merlet P, Syrota A, Slama MS, Le Guludec D.
Medicine (Baltimore)
. 2006 Jul;85(4):229-38.
PMID: 16862048
[PubMed - indexed for MEDLINE]
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30.
TTR-familial amyloid polyneuropathy--neurological aspects.
Said G, Planté-Bordeneuve V.
Amyloid
. 2012 Jun;19 Suppl 1:25-7.
PMID: 22620963
[PubMed - in process]
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31.
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.
Valleix S, Gillmore JD, Bridoux F, Mangione PP, Dogan A, Nedelec B, Boimard M, Touchard G, Goujon JM, Lacombe C, Lozeron P, Adams D, Lacroix C, Maisonobe T, Planté-Bordeneuve V, Vrana JA, Theis JD, Giorgetti S, Porcari R, Ricagno S, Bolognesi M, Stoppini M, Delpech M, Pepys MB, Hawkins PN, Bellotti V.
N Engl J Med
. 2012 Jun 14;366(24):2276-83.
PMID: 22693999
[PubMed - indexed for MEDLINE]
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32.
Parent-of-origin effect in transthyretin related amyloid polyneuropathy.
Bonaïti B, Alarcon F, Bonaïti-Pellié C, Planté-Bordeneuve V.
Amyloid. 2009;16(3):149-50. No abstract available.
PMID: 19626480
[PubMed - indexed for MEDLINE]
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33.
Operative risks of domino liver transplantation for the FAP liver donor and the FAP liver recipient.
Azoulay D, Salloum C, Samuel D, Planté-Bordeneuve V.
Amyloid. 2012 Jun;19 Suppl 1:73-4.
PMID: 22620970
[PubMed - in process]
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34.
Genetic study of transthyretin amyloid neuropathies: carrier risks among French and Portuguese families.
Planté-Bordeneuve V, Carayol J, Ferreira A, Adams D, Clerget-Darpoux F, Misrahi M, Said G, Bonaïti-Pellié C.
J Med Genet
. 2003 Nov;40(11):e120. No abstract available.
PMID: 14627687
[PubMed - indexed for MEDLINE]
Free PMC Article
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35.
Familial amyloid polyneuropathy: a clinico-pathologic study.
Said G, Planté-Bordeneuve V.
J Neurol Sci
. 2009 Sep 15;284(1-2):149-54. Epub 2009 May 24.
PMID: 19467548
[PubMed - indexed for MEDLINE]
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36.
Marked systemic amyloid angiopathy in patients with val 107 transthyretin mutation.
Authier FJ, Lechapt-Zalcman E, Mussini JM, Plante-Bordeneuve V, Eizenbaum JF, Jacobson DR, Gherardi RK.
J Clin Neuromuscul Dis
. 1999 Dec;1(2):82-5.
PMID: 19078558
[PubMed - in process]
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37.
[The diagnosis and management of familial amyloid polyneuropathy].
Planté-Bordeneuve V.
Rev Neurol (Paris)
. 2006 Nov;162(11):1138-46. Review. French.
PMID: 17086153
[PubMed - indexed for MEDLINE]
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38.
Subacute sensory neuropathy associated with Hodgkin's disease.
Plante-Bordeneuve V, Baudrimont M, Gorin NC, Gherardi RK.
J Neurol Sci
. 1994 Feb;121(2):155-8.
PMID: 8158207
[PubMed - indexed for MEDLINE]
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