Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross‐over controlled trial in a rare disease von Gaillard, S., Dupuis‐Girod, S., Boutitie, F., Rivière, S., Morinière, S., Hatron, P.‐Y., Manfredi, G., Kaminsky, P., Capitaine, A.‐L., Roy, P., Gueyffier, F., Plauchu, H.

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Hereditary hemorrhagic telangiectasia: from molecular biology to patient care von DUPUIS‐GIROD, S., BAILLY, S., PLAUCHU, H.

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Immunological abnormalities associated with hereditary haemorrhagic telangiectasia von Guilhem, A., Malcus, C., Clarivet, B., Plauchu, H., Dupuis‐Girod, S.

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The new Ghent criteria for Marfan syndrome: what do they change? von Faivre, L, Collod-Beroud, G, Adès, L, Arbustini, E, Child, A, Callewaert, BL, Loeys, B, Binquet, C, Gautier, E, Mayer, K, Arslan-Kirchner, M, Grasso, M, Beroud, C, Hamroun, D, Bonithon-Kopp, C, Plauchu, H, Robinson, PN, De Backer, J, Coucke, P, Francke, U, Bouchot, O, Wolf, JE, Stheneur, C, Hanna, N, Detaint, D, De Paepe, A, Boileau, C, Jondeau, G

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Psychosocial quality of life in hereditary haemorrhagic telangiectasia patients von LOAËC, Marjorie, MORINIERE, Sylvain, HITIER, Martin, FERRANT, Ophélie, PLAUCHU, Henry, BABIN, Emmanuel

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Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands von Faivre, L, Collod-Beroud, G, Child, A, Callewaert, B, Loeys, B L, Binquet, C, Gautier, E, Arbustini, E, Mayer, K, Arslan-Kirchner, M, Stheneur, C, Kiotsekoglou, A, Comeglio, P, Marziliano, N, Halliday, D, Beroud, C, Bonithon-Kopp, C, Claustres, M, Plauchu, H, Robinson, P N, Adès, L, De Backer, J, Coucke, P, Francke, U, De Paepe, A, Boileau, C, Jondeau, G

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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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Connexin 26 gene linked to a dominant deafness von Denoyelle, Françoise, Lina-Granade, Genevieve, Plauchu, Henri, Bruzzone, Roberto, Chaïb, Hassan, Lévi-Acobas, Fabienne, Weil, Dominique, Petit, Christine

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What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome? von Coron, F., Rousseau, T., Jondeau, G., Gautier, E., Binquet, C., Gouya, L., Cusin, V., Odent, S., Dulac, Y., Plauchu, H., Collignon, P., Delrue, M.-A., Leheup, B., Joly, L., Huet, F., Thevenon, J., Mace, G., Cassini, C., Thauvin-Robinet, C., Wolf, J. E., Hanna, N., Sagot, P., Boileau, C., Faivre, L.

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Visceral manifestations in hereditary haemorrhagic telangiectasia type 2 von Abdalla, S A, Geisthoff, U W, Bonneau, D, Plauchu, H, McDonald, J, Kennedy, S, Faughnan, M E, Letarte, M

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Cancer patients who experienced diagnostic genetic testing for cancer susceptibility: Reactions and behavior after the disclosure of a positive test result von BONADONA, Valérie, SALTEL, Pierre, PUISIEUX, Alain, LASSET, Christine, DESSEIGNE, Francoise, MIGNOTTE, Hervé, SAURIN, Jean-Christophe, QING WANG, SINILNIKOVA, Olga, GIRAUD, Sophie, FREYER, Gilles, PLAUCHU, Henri

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STROKE FOLLOWING PULMONARY ARTERIOVENOUS FISTULA EMBOLIZATION IN A PATIENT WITH HHT von FELIX, S, JEANNIN, S, GOIZET, C, THAMBO, J. B, GIRAUD, S, PLAUCHU, H, MONTAUDON, M, SIBON, I

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International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia von Faughnan, M E, Palda, V A, Garcia-Tsao, G, Geisthoff, U W, McDonald, J, Proctor, D D, Spears, J, Brown, D H, Buscarini, E, Chesnutt, M S, Cottin, V, Ganguly, A, Gossage, J R, Guttmacher, A E, Hyland, R H, Kennedy, S J, Korzenik, J, Mager, J J, Ozanne, A P, Piccirillo, J F, Picus, D, Plauchu, H, Porteous, M E M, Pyeritz, R E, Ross, D A, Sabba, C, Swanson, K, Terry, P, Wallace, M C, Westermann, C J J, White, R I, Young, L H, Zarrabeitia, R

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A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q von Vincent, P., Plauchu, H., Hazan, J., Fauré, S., Weissenbach, J., Godet, J.

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Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia -- results of extensive screening von Buscarini, E, Danesino, C, Olivieri, C, Lupinacci, G, De Grazia, F, Reduzzi, L, Blotta, P, Gazzaniga, P, Pagella, F, Grosso, M, Pongiglione, G, Buscarini, L, Plauchu, H, Zambelli, A

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Infantile ascending hereditary spastic paralysis (IAHSP): Clinical features in 11 families von LESCA, G, EYMARD-PIERRE, E, BOESPFLUG-TANGUY, O, BERTINI, E, SANTORELLI, F. M, CUSMAI, R, DI CAPUA, M, VALENTE, E. M, ATTIA-SOBOL, J, PLAUCHU, H, LEUZZI, V, PONZONE, A

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Familial thoracic aortic aneurysm/dissection with patent ductus arteriosus: genetic arguments for a particular pathophysiological entity von Khau Van Kien, Philippe, Wolf, Jean-Eric, Mathieu, Flavie, Zhu, Limin, Salve, Nicolas, Lalande, Alain, Bonnet, Caroline, Lesca, Gaëtan, Plauchu, Henri, Dellinger, Arnaud, Nivelon-Chevallier, Annie, Brunotte, François, Jeunemaitre, Xavier

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Liver transplantation resolves the hyperdynamic circulation in hereditary hemorrhagic telangiectasia with hepatic involvement von Boillot, Olivier, Bianco, Francesco, Viale, Jean-Paul, Mion, Francois, Mechet, Isabelle, Gille, Danielle, Delaye, Jacques, Paliard, Pierre, Plauchu, Henri

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Mutation Analysis and Embryonic Expression of the HLXB9 Currarino Syndrome Gene von Hagan, D.M., Ross, A.J., Strachan, T., Lynch, S.A., Ruiz-Perez, V., Wang, Y.M., Scambler, P., Custard, E., Reardon, W., Hassan, S., Muenke, M., Nixon, P., Papapetrou, C., Winter, R.M., Edwards, Y., Morrison, K., Barrow, M., Cordier-Alex, M.P., Correia, P., Galvin-Parton, P.A., Gaskill, S., Gaskin, K.J., Garcia-Minaur, S., Gereige, R., Hayward, R., Homfray, T., McKeown, C., Murday, V., Plauchu, H., Shannon, N., Spitz, L., Lindsay, S.

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A Locus for Autosomal Dominant Colobomatous Microphthalmia Maps to Chromosome 15q12-q15 von Morlé, L., Bozon, M., Zech, J.-C., Alloisio, N., Raas-Rothschild, A., Philippe, C., Lambert, J.-C., Godet, J., Plauchu, H., Edery, P.

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