FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Sophie Valleix

Research Profile

Disorders

Concepts & Ideas

Pedigree

Physiology

Procedures

Anatomy

Cornea

Chemicals & Drugs

Geographic Areas

France

Genes & Molecular Sequences

Dominant Genes

Co-author Network

Publications

TOP 3
Sophie Valleix; Julie A Vrana; david adams; Mathieu Boimard; Martino Bolognesi; Frank Bridoux; Marc Delpech; Ahmet Dogan; Julian D Gillmore; Sofia Giorgetti; Jean-Michel Goujon; Philip N Hawkins; Corinne Lacombe; Catherine Lacroix; Pierre Lozeron; Thierry Maisonobe; Palma P Mangione; Brigitte Nedelec; Mark B Pepys; Violaine Planté-Bordeneuve; Riccardo Porcari; Stefano Ricagno; Monica Stoppini; Jason D Theis; Guy Touchard; Vittorio Bellotti
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.
Antoine P Brézin; Marc Delpech; Brigitte Nedelec; Pierre-Raphael Rothschild; Amandine Barjol; Sophie Valleix
A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features.
Gilles Grateau; Sophie Valleix; patrice callard
[Multisystemic amyloidosis in 2007].

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Sophie Valleix (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Sophie Valleix; Julie A Vrana; david adams; Mathieu Boimard; Martino Bolognesi; Frank Bridoux; Marc Delpech; Ahmet Dogan; Julian D Gillmore; Sofia Giorgetti; Jean-Michel Goujon; Philip N Hawkins; Corinne Lacombe; Catherine Lacroix; Pierre Lozeron; Thierry Maisonobe; Palma P Mangione; Brigitte Nedelec; Mark B Pepys; Violaine Planté-Bordeneuve; Riccardo Porcari; Stefano Ricagno; Monica Stoppini; Jason D Theis; Guy Touchard; Vittorio Bellotti
Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.
The New England journal of medicine 2012;366(24):2276-83.
2011: Antoine P Brézin; Marc Delpech; Brigitte Nedelec; Pierre-Raphael Rothschild; Amandine Barjol; Sophie Valleix
A new VCAN/versican splice acceptor site mutation in a French Wagner family associated with vascular and inflammatory ocular features.
Molecular vision 2011;17():1669-78.
2007: Gilles Grateau; Sophie Valleix; patrice callard
[Multisystemic amyloidosis in 2007].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 2007;28(5):281-3.
2006: Sophie Valleix; Florence Niel; Brigitte Nedelec; Marie-Paule Algros; Claire Schwartz; Bernard Delbosc; Marc Delpech; Bernadette Kantelip
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.
American journal of human genetics 2006;79(2):358-64.
2006: Brigitte Granel; Sophie Valleix; Jacques Serratrice; Patrick Chérin; Antonio Texeira; Patrick Disdier; Pierre-Jean Weiller; Gilles Grateau
Lysozyme amyloidosis: report of 4 cases and a review of the literature.
Medicine 2006;85(1):66-73.
2006: Sophie Valleix; Brigitte Nedelec; Florence Rigaudiere; Paul Dighiero; Yves Pouliquen; Gilles Renard; Jean-François Le Gargasson; Marc Delpech
H244R VSX1 is associated with selective cone ON bipolar cell dysfunction and macular degeneration in a PPCD family.
Investigative ophthalmology & visual science 2006;47(1):48-54.
2005: Brigitte Granel; Jacques Serratrice; Patrick Disdier; Pierre-Jean Weiller; Sophie Valleix; Gilles Grateau; Dominique Droz
Underdiagnosed amyloidosis: amyloidosis of lysozyme variant.
The American journal of medicine 2005;118(3):321-2.
2003: Florence Niel; Pierre Ellies; Paul Dighiero; Jeannette Soria; Celia Sabbagh; Chankannira San; Gilles Renard; Marc Delpech; Sophie Valleix
Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophy.
Investigative ophthalmology & visual science 2003;44(7):2949-53.
2002: Nadine Magy; Sophie Valleix; Gilles Grateau; Marie-Paule Algros; Romain Guillemain; Bernadette Kantelip; Marc Delpech; Jean-Louis Dupond
Transthyretin mutation (TTRGly47Ala) associated with familial amyloid polyneuropathy in a French family.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2002;9(4):272-5.
2002: Sophie Valleix; Christine Vinciguerra; Jean-Maurice Lavergne; Marco Leuer; Marc Delpech; Claude Negrier
Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A.
Blood 2002;100(8):3034-6.
2002: Brigitte Granel; Jacques Serratrice; Sophie Valleix; Gilles Grateau; Dominique Droz; Jacques Lafon; Marie-Christine Sault; Bernard Chaudier; Patrick Disdier; René Laugier; Marc Delpech; Pierre-Jean Weiller
A family with gastrointestinal amyloidosis associated with variant lysozyme.
Gastroenterology 2002;123(4):1346-9.
2002: Pierre Ellies; Gilles Renard; Sophie Valleix; Pierre-Yves Boelle; Paul Dighiero
Clinical outcome of eight BIGH3-linked corneal dystrophies.
Ophthalmology 2002;109(4):793-7.
2002: Sophie Valleix; Séverine Drunat; Jean-Baptiste Philit; Daniel Adoue; Jean-Charles Piette; Dominique Droz; Brigitte MacGregor; Denis Canet; Marc Delpech; Gilles Grateau
Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family.
Kidney international 2002;61(3):907-12.
2001: Emmanuel Ellie; Fabrice Camou; Anne Vital; C Rummens; Gilles Grateau; Marc Delpech; Sophie Valleix
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu).
Neurology 2001;57(1):135-7.
2001: Gilles Grateau; Sophie Valleix; Marc Delpech
[Hereditary amyloidosis].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 2001;22 Suppl 1():13s-15s.
2001: Paul Dighiero; Florence Niel; Pierre Ellies; François D'Hermies; Michèle Savoldelli; Gilles Renard; Marc Delpech; Sophie Valleix
Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene.
Ophthalmology 2001;108(4):818-23.
2000: R Favier; Jean-Maurice Lavergne; J M Costa; C Caron; Claudine Mazurier; M Viémont; Marc Delpech; Sophie Valleix
Unbalanced X-chromosome inactivation with a novel FVIII gene mutation resulting in severe hemophilia A in a female.
Blood 2000;96(13):4373-5.
2000: Paul Dighiero; Pierre Ellies; Sophie Valleix; François D'Hermies; Michèle Savoldelli; Yves Pouliquen; Jean-Marc Legeais; Gilles Renard
[Avellino dystrophy. Current diagnostic criteria].
Journal français d'ophtalmologie 2000;23(7):735-7.
2000: Paul Dighiero; Sophie Valleix; François D'Hermies; Séverine Drunat; Pierre Ellies; Michèle Savoldelli; Yves Pouliquen; Marc Delpech; Jean-Marc Legeais; Gilles Renard
Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L mutation of the BIGH3 gene.
Ophthalmology 2000;107(7):1353-7.
2000: Gilles Grateau; H Lebrazi; Sophie Valleix; E Hachulla; Marc Delpech; R Saïle
[Diagnostic strategy in amyloidosis].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 2000;21(6):517-23.
2000: Paul Dighiero; Séverine Drunat; François D'Hermies; Gilles Renard; Marc Delpech; Sophie Valleix
A novel variant of granular corneal dystrophy caused by association of 2 mutations in the TGFBI gene-R124L and DeltaT125-DeltaE126.
Archives of ophthalmology 2000;118(6):814-8.
2000: Paul Dighiero; Séverine Drunat; Pierre Ellies; François D'Hermies; Michèle Savoldelli; Jean-Marc Legeais; Gilles Renard; Marc Delpech; Gilles Grateau; Sophie Valleix
A new mutation (A546T) of the betaig-h3 gene responsible for a French lattice corneal dystrophy type IIIA.
American journal of ophthalmology 2000;129(2):248-51.
1999: Sophie Valleix; J C Jeanny; S Elsevier; Rajiv L Joshi; P Fayet; Danielle Bucchini; Marc Delpech
Expression of human F8B, a gene nested within the coagulation factor VIII gene, produces multiple eye defects and developmental alterations in chimeric and transgenic mice.
Human molecular genetics 1999;8(7):1291-301.
1997: Sophie Valleix; K Nafa; Natalie Stieltjes; M Viemont; Y Sultan; Jean-Claude Kaplan; Marc Delpech
Prevalence, male germ-line origin and new patterns of inversions in haemophilia A.
Annales de génétique 1997;40(1):35-40.
1995: Stylianos Antonarakis; Judith P. Rossiter; M Young; J Horst; P de Moerloose; S S Sommer; Rhett P Ketterling; Haig Kazazian ; Claude Négrier; Christine Vinciguerra; Jane Gitschier; Michel Goossens; Emmanuelle Girodon; N Ghanem; F Plassa; Jean-Maurice Lavergne; M Vidaud; J M Costa; Yves Laurian; S W Lin; S R Lin; M C Shen; David Lillicrap; S A Taylor; S Windsor; Sophie Valleix; Khedoudja Nafa; Y Sultan; Marc Delpech; C L Vnencak-Jones; J A Phillips; R C Ljung; E Koumbarelis; AE Gialeraki; Titika Mandalaki; P Vincent Jenkins; P W Collins; K John Pasi; Anne C Goodeve; Ian R Peake; F Eric Preston; Marianne Schwartz; E Scheibel; Jørgen Ingerslev; D N Cooper; D S Millar; V V Kakkar; F Giannelli; J A Naylor; E F Tizzano; Montserrat Baiget; M Domenech; Carme Altisent; J Tusell; M Beneyto; J I Lorenzo; Christine Gaucher; Claudine Mazurier; Kathelijne Peerlinck; Gert Matthijs; J J Cassiman; J Vermylen; Pier Giorgio Mori; M Acquila; Daniela Caprino; H Inaba
Factor VIII gene inversions in severe hemophilia A: results of an international consortium study.
Blood 1995;86(6):2206-12.