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Nicole Ravisé

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Alexandre Chojnowski; Nicole Ravisé; Corinne Bachelin; Christel Depienne; Merle Ruberg; Bernard Brugg; Jocelyn Laporte; Anne Baron-Van Evercooren; Eric LeGuern
Silencing of the Charcot-Marie-Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells.
Hamid Azzedine; Nicole Ravisé; Christophe Verny; A Gabrëels-Festen; M Lammens; Djamel Grid; Jean-Michel Vallat; Garry Durosier; Jan Senderek; S Nouioua; Tarik Hamadouche; Ahmed Bouhouche; Angele Guilbot; Claudia Stendel; Merle Ruberg; Alexis Brice; Nazha Birouk; Odile Dubourg; Meriem Tazir; Eric LeGuern
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.
Christophe Verny; Nicole Ravisé; Anne-Louise Leutenegger; F Pouplard; Odile Dubourg; Sandrine Tardieu; Frédéric Dubas; Alexis Brice; Emmanuelle Genin; Eric LeGuern
Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family.

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All Publications

2007: Alexandre Chojnowski; Nicole Ravisé; Corinne Bachelin; Christel Depienne; Merle Ruberg; Bernard Brugg; Jocelyn Laporte; Anne Baron-Van Evercooren; Eric LeGuern
Silencing of the Charcot-Marie-Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells.
Neurobiology of disease 2007;26(2):323-31.
2006: Hamid Azzedine; Nicole Ravisé; Christophe Verny; A Gabrëels-Festen; M Lammens; Djamel Grid; Jean-Michel Vallat; Garry Durosier; Jan Senderek; S Nouioua; Tarik Hamadouche; Ahmed Bouhouche; Angele Guilbot; Claudia Stendel; Merle Ruberg; Alexis Brice; Nazha Birouk; Odile Dubourg; Meriem Tazir; Eric LeGuern
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.
Neurology 2006;67(4):602-6.
2004: Christophe Verny; Nicole Ravisé; Anne-Louise Leutenegger; F Pouplard; Odile Dubourg; Sandrine Tardieu; Frédéric Dubas; Alexis Brice; Emmanuelle Genin; Eric LeGuern
Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family.
Neurology 2004;63(8):1527-9.
2003: Nicole Ravisé; Odile Dubourg; Sandrine Tardieu; Françoise Aurias; Monique Mercadiel; Philippe Coullin; Merle Ruberg; Martin Catala; Sylvie Lesourd; Alexis Brice; Eric LeGuern
Rapid detection of 17p11.2 rearrangements by FISH without cell culture (direct FISH, DFISH): a prospective study of 130 patients with inherited peripheral neuropathies.
American journal of medical genetics. Part A 2003;118A(1):43-8.
2001: Anne-Sophie Lebre; L Jamot; Junko Takahashi; Nathalie Spassky; corinne leprince; Nicole Ravisé; Cecilia Zander; Hiroto Fujigasaki; P Kussel-Andermann; Charles Duyckaerts; Jacques Camonis; Alexis Brice
Ataxin-7 interacts with a Cbl-associated protein that it recruits into neuronal intranuclear inclusions.
Human molecular genetics 2001;10(11):1201-13.
2001: Angele Guilbot; A Williams; Nicole Ravisé; Christophe Verny; Alexis Brice; Diane L Sherman; Peter J Brophy; Eric LeGuern; Valérie Delague; Corinne Bareil; André Mégarbané; Mireille Claustres
A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease.
Human molecular genetics 2001;10(4):415-21.
1999: Angele Guilbot; Nicole Ravisé; Ahmed Bouhouche; Philippe Coullin; Nazha Birouk; Thierry Maisonobe; Thierry Kuntzer; C Vial; Djamel Grid; Alexis Brice; Eric LeGuern
Genetic, cytogenetic and physical refinement of the autosomal recessive CMT linked to 5q31-q33: exclusion of candidate genes including EGR1.
European journal of human genetics : EJHG 1999;7(8):849-59.
1999: Angele Guilbot; M Kessali; Nicole Ravisé; Tarik Hammadouche; Ahmed Bouhouche; Thierry Maisonobe; Djamel Grid; Alexis Brice; Eric LeGuern
The autosomal recessive form of CMT disease linked to 5q31-q33.
Annals of the New York Academy of Sciences 1999;883():453-6.
1999: Angele Guilbot; M Kessali; Nicole Ravisé; Tarik Hammadouche; Ahmed Bouhouche; Thierry Maisonobe; Djamel Grid; Alexis Brice; Eric LeGuern
The autosomal recessive form of CMT disease linked to 5q31-q33.
Annals of the New York Academy of Sciences 1999;883():56-9.
1998: J Lopes; Nicole Ravisé; Antoon Vandenberghe; Francesc Palau; V Ionasescu; M Mayer; Nicolas Lévy; Nicholas W Wood; N Tachi; Pierre Bouche; Philippe Latour; Merle Ruberg; Alexis Brice; Eric LeGuern
Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination.
Human molecular genetics 1998;7(1):141-8.
1996: Eric LeGuern; Angele Guilbot; M Kessali; Nicole Ravisé; JP Tassin; Thierry Maisonobe; Djamel Grid; Alexis Brice
Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.
Human molecular genetics 1996;5(10):1685-8.
1996: Eric LeGuern; Riadh Gouider; Nicole Ravisé; J Lopes; Sandrine Tardieu; M Gugenheim; Nacer Abbas; Pierre Bouche; Yves Agid; Alexis Brice
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
Human molecular genetics 1996;5(1):103-6.
1995: Eric LeGuern; Riadh Gouider; J Lopes; Nacer Abbas; M Gugenheim; Sandrine Tardieu; Nicole Ravisé; Jean-Marc Léger; Jean-Michel Vallat; Pierre Bouche
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group.
Human molecular genetics 1995;4(9):1673-4.
1994: P Couillin; E Le Guern; A Vignal; C Fizames; Nicole Ravisé; D Delportes; I Reguigne; M F Rosier; C Junien; Veronica van Heyningen
Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic map.
Genomics 1994;21(2):379-87.
1994: Giovanni Stevanin; E Le Guern; Nicole Ravisé; H Chneiweiss; Alexandra Dürr; G Cancel; A Vignal; A L Boch; Merle Ruberg; C Penet
A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.
American journal of human genetics 1994;54(1):11-20.
1994: E Le Guern; Franck Sturtz; M Gugenheim; Riadh Gouider; C Bonnebouche; Nicole Ravisé; P M Gonnaud; Sandrine Tardieu; Pierre Bouche; G Chazot
Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP).
Cytogenetics and cell genetics 1994;65(4):261-4.
1992: Alexis Brice; Nicole Ravisé; Giovanni Stevanin; M Gugenheim; Pierre Bouche; C Penet; Yves Agid
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.
Journal of medical genetics 1992;29(11):807-12.
1991: P Couillin; R Mollicone; M C Grisard; A Gibaud; Nicole Ravisé; J Feingold; Rafael Oriol
Chromosome 11q localization of one of the three expected genes for the human alpha-3-fucosyltransferases, by somatic hybridization.
Cytogenetics and cell genetics 1991;56(2):108-11.
1989: P Couillin; M Azoulay; I Henry; Nicole Ravisé; M C Grisard; Cécile Jeanpierre; F Barichard; P Metezeau; Jean-Jacques Candelier; W Lewis
Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.
Human genetics 1989;82(2):171-8.
1987: P Couillin; Nicole Ravisé; J M Afoutou; R Chaïbi; M Azoulay; J Hors; J F Oury; J Boué; A Boué
[HLA and molar pregnancies (triploidies, hydatidiform moles and choriocarcinoma). Etiological and epidemiological study].
Annales de génétique 1987;30(4):197-208.
1986: P Couillin; Nicole Ravisé; J Hors; J Feingold; R Rappaport; F Kuttenn; A Boué
[HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population].
Pathologie-biologie 1986;34(6):789-94.
1985: P Couillin; J M Afoutou; O Faye; Nicole Ravisé; P Correa; A Boué
Androgenetic origin of African complete hydatidiform moles demonstrated by HLA markers.
Human genetics 1985;71(2):113-6.