Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Valayanopoulos Vassili"'
Autor:
Stirnemann Jérôme, Vigan Marie, Hamroun Dalil, Heraoui Djazia, Rossi-Semerano Linda, Berger Marc G, Rose Christian, Camou Fabrice, de Roux-Serratrice Christine, Grosbois Bernard, Kaminsky Pierre, Robert Alain, Caillaud Catherine, Froissart Roselyne, Levade Thierry, Masseau Agathe, Mignot Cyril, Sedel Frédéric, Dobbelaere Dries, Vanier Marie T, Valayanopoulos Vassili, Fain Olivier, Fantin Bruno, de Villemeur Thierry, Mentré France, Belmatoug Nadia
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 77 (2012)
Abstract Background Clinical features, complications and treatments of Gaucher’s disease (GD), a rare autosomal–recessive disorder due to a confirmed lysosomal enzyme (glucocerebrosidase) deficiency, are described. Methods All patients with known
Externí odkaz:
https://doaj.org/article/d6f365a1e786437fa298ec7657985b69
Autor:
Boddaert, Nathalie, Ribeiro, Maria, Touati, Guy, Mention, Karine, Valayanopoulos, Vassili, Nihoul-Fékété, Claire, Brunelle, Francis, de Lonlay, Pascale
Publikováno v:
Médecine/Sciences; November 2005, Vol. 21 Issue: 11 p981-986, 6p
Autor:
Boddaert N; Service de radiologie pédiatrique, ERM 0205, Hôpital Necker Enfants-Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France. nathalie.boddaert@nck.ap-hop-paris.fr, Ribeiro M, Touati G, Mention K, Valayanopoulos V, Nihoul-Fékété C, Brunelle F, de Lonlay P
Publikováno v:
Medecine sciences : M/S [Med Sci (Paris)] 2005 Nov; Vol. 21 (11), pp. 981-6.