Prevalence of Hemoplasma spp. positivity in potential feline blood donors and study of the association with selected clinical variables von Roels, Elodie, Debie, Chiara, Giraud, Sophie, Ferreira, Rui, Gommeren, Kris

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UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population von Romanet, Pauline, Mohamed, Amira, Giraud, Sophie, Odou, Marie-Françoise, North, Marie-Odile, Pertuit, Morgane, Pasmant, Eric, Coppin, Lucie, Guien, Céline, Calender, Alain, Borson-Chazot, Françoise, Béroud, Christophe, Goudet, Pierre, Barlier, Anne

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Genetic Testing in Pheochromocytoma or Functional Paraganglioma von AMAR, Laurence, BERTHERAT, Jérome, NICCOLI-SIRE, Patricia, RICHARD, Stéphane, ROHMER, Vincent, SADOUL, Jean-Louis, STROMPF, Laurence, SCHLUMBERGER, Martin, BERTAGNA, Xavier, PLOUIN, Pierre-Francois, JEUNEMAITRE, Xavier, GIMENEZ-ROQUEPLO, Anne-Paule, BAUDIN, Eric, AJZENBERG, Christiane, BRESSAC-DE PAILLERETS, Brigitte, CHABRE, Olivier, CHAMONTIN, Bernard, DELEMER, Brigitte, GIRAUD, Sophie, MURAT, Amaud

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Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia von Giraud, Sophie, Bardel, Claire, Dupuis-Girod, Sophie, Carette, Marie-France, Gilbert-Dussardier, Brigitte, Riviere, Sophie, Saurin, Jean-Christophe, Eyries, Mélanie, Patri, Sylvie, Decullier, Evelyne, Calender, Alain, Lesca, Gaëtan

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Genomic expression and single-nucleotide polymorphism profiling discriminates chromophobe renal cell carcinoma and oncocytoma von Tan, Min-Han, Wong, Chin Fong, Tan, Hwei Ling, Yang, Ximing J, Ditlev, Jonathon, Matsuda, Daisuke, Khoo, Sok Kean, Sugimura, Jun, Fujioka, Tomoaki, Furge, Kyle A, Kort, Eric, Giraud, Sophie, Ferlicot, Sophie, Vielh, Philippe, Amsellem-Ouazana, Delphine, Debré, Bernard, Flam, Thierry, Thiounn, Nicolas, Zerbib, Marc, Benoît, Gérard, Droupy, Stéphane, Molinié, Vincent, Vieillefond, Annick, Tan, Puay Hoon, Richard, Stéphane, Teh, Bin Tean

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Functional analysis of the BMP9 response of ALK1 mutants from HHT2 patients: a diagnostic tool for novel ACVRL1 mutations von Ricard, Nicolas, Bidart, Marie, Mallet, Christine, Lesca, Gaetan, Giraud, Sophie, Prudent, Renaud, Feige, Jean-Jacques, Bailly, Sabine

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Characterization of endolymphatic sac tumors and von Hippel-Lindau disease in the International Endolymphatic Sac Tumor Registry von Bausch, Birke, Wellner, Ulrich, Peyre, Mathieu, Boedeker, Carsten C., Hes, Frederik J., Anglani, Mariagiulia, de Campos, Jose M., Kanno, Hiroshi, Maher, Eamonn R., Krauss, Tobias, Sansó, Gabriela, Barontini, Marta, Letizia, Claudio, Hader, Claudia, Schiavi, Francesca, Zanoletti, Elisabetta, Suárez, Carlos, Offergeld, Christian, Malinoc, Angelica, Zschiedrich, Stefan, Glasker, Sven, Bobin, Serge, Sterkers, Olivier, Ba Huy, Patrice Tran, Giraud, Sophie, Links, Thera, Eng, Charis, Opocher, Giuseppe, Richard, Stephane, Neumann, Hartmut P. H.

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Genetic variants of Adam17 differentially regulate TGFβ signaling to modify vascular pathology in mice and humans von Kawasaki, Kyoko, Freimuth, Julia, Meyer, Dominique S., Lee, Marie M., Tochimoto-Okamoto, Akiko, Benzinou, Michael, Clermont, Frederic F., Wu, Gloria, Roy, Ritu, Letteboer, Tom G. W., van Amstel, Johannes Kristian Ploos, Giraud, Sophie, Dupuis-Girod, Sophie, Lesca, Gaeten, Westermann, Cornelius J. J., Coffey, Robert J., Akhurst, Rosemary J.

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Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network von Lesca, Gaëtan, Olivieri, Carla, Burnichon, Nelly, Pagella, Fabio, Carette, Marie-France, Gilbert-Dussardier, Brigitte, Goizet, Cyril, Roume, Joelle, Rabilloud, Muriel, Saurin, Jean-Christophe, Cottin, Vincent, Honnorat, Jerome, Coulet, Florence, Giraud, Sophie, Calender, Alain, Danesino, Cesare, Buscarini, Elisabetta, Plauchu, Henri

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Vitreoretinal Surgery for Severe Retinal Capillary Hemangiomas in Von Hippel–Lindau Disease von Gaudric, Alain, MD, Krivosic, Valérie, MD, Duguid, Graham, MD, FRCS, Massin, Pascale, MD, PhD, Giraud, Sophie, MD, PhD, Richard, Stéphane, MD, PhD

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new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene von Lim, Derek H.K, Rehal, Pauline K, Nahorski, Michael S, Macdonald, Fiona, Claessens, Tijs, Van Geel, Michel, Gijezen, Lieke, Gille, Johan J.P, Giraud, Sophie, Richard, Stephane, van Steensel, Maurice, Menko, Fred H, Maher, Eamonn R

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Birt-Hogg-Dubé syndrome: diagnosis and management von Menko, Fred H, Dr, van Steensel, Maurice AM, MD, Giraud, Sophie, MD, Friis-Hansen, Lennart, MD, Richard, Stéphane, Prof, Ungari, Silvana, MD, Nordenskjöld, Magnus, Prof, Hansen, Thomas vO, MSc, Solly, John, PhD, Maher, Eamonn R, Prof

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Hemorrhagic Hereditary Telangiectasia (Rendu-Osler Disease) and Infectious Diseases: An Underestimated Association von Girod, Sophie Dupuis, Giraud, Sophie, Decullier, Evelyne, Lesca, Gaetan, Cottin, Vincent, Faure, Frédéric, Merrot, Olivier, Saurin, Jean-Christophe, Cordier, Jean-François, Plauchu, Henri

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(Not) wanting to choose: outside agencies at work in assisted reproductive technology von Giraud, Anne-Sophie

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Familial Non-VHL Clear Cell (Conventional) Renal Cell Carcinoma: Clinical Features, Segregation Analysis, and Mutation Analysis of FLCN von WOODWARD, Emma R, RICKETTS, Christopher, ESCUDIER, Bernard, LATIF, Farida, RICHARD, Stéphane, MAHERL, Eamonn R, KILLICK, Pip, GAD, Sophie, MORRIS, M. R, KAVALIER, Fred, HODGSON, Shirleyv, GIRAUD, Sophie, BRESSAC-DE PAILLERETS, Brigitte, CHAPMAN, Cyril

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Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression von Klomp, Jeff A, Petillo, David, Niemi, Natalie M, Dykema, Karl J, Chen, Jindong, Yang, Ximing J, Sääf, Annika, Zickert, Peter, Aly, Markus, Bergerheim, Ulf, Nordenskjöld, Magnus, Gad, Sophie, Giraud, Sophie, Denoux, Yves, Yonneau, Laurent, Méjean, Arnaud, Vasiliu, Viorel, Richard, Stéphane, MacKeigan, Jeffrey P, Teh, Bin T, Furge, Kyle A

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Evaluation of previously nonscreened hereditary hemorrhagic telangiectasia patients shows frequent liver involvement and early cardiac consequences von Gincul, Rodica, Lesca, Gaetan, Gelas‐Dore, Bénédicte, Rollin, Nathalie, Barthelet, Martine, Dupuis‐Girod, Sophie, Pilleul, Franck, Giraud, Sophie, Plauchu, Henri, Saurin, Jean‐Christophe

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Natural History of Supratentorial Hemangioblastomas in von Hippel-Lindau Disease von Peyre, Matthieu, David, Philippe, Van Effenterre, Remy, François, Patrick, Thys, Myriam, Emery, Evelyne, Redondo, Aimée, Decq, Philippe, Aghakhani, Nozar, Parker, Fabrice, Tadié, Marc, Lacroix, Catherine, Bhangoo, Ranjeev, Giraud, Sophie, Richard, Stéphane

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High diagnostic and clinical impact of small-bowel capsule endoscopy in patients with hereditary hemorrhagic telangiectasia with overt digestive bleeding and/or severe anemia von Grève, Emilie, MD, Moussata, Driffa, MD, Gaudin, Jean Louis, MD, Lapalus, Marie-Georges, MD, Giraud, Sophie, MD, Dupuis-Girod, Sophie, MD, Calender, Alain, MD, PhD, Plauchu, Henri, MD, PhD, Saurin, Jean-Christophe, MD, PhD

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Intensity-dependent constitutional MLH1 promoter methylation leads to early onset of colorectal cancer by affecting both alleles von Auclair, Jessie, Vaissière, Thomas, Desseigne, Françoise, Lasset, Christine, Bonadona, Valérie, Giraud, Sophie, Saurin, Jean-Christophe, Joly, Marie-Odile, Leroux, Dominique, Faivre, Laurence, Audoynaud, Carole, Montmain, Gilles, Ruano, Eric, Herceg, Zdenko, Puisieux, Alain, Wang, Qing

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