Severe Hypoglycemia in a Nondiabetic Old Woman Treated with a Single Oral Dose of Hydroxychloroquine for Covid-19

Autor: Dina Selma Zekry Berger, Christine De Roux Serratrice, Davide Moro, Giacomo Gastaldi

Publikováno v: Journal of Geriatric Medicine and Gerontology, Vol. 6, No 2 (2020) P. 091

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cf5d59d225159c60f894fa6fe9cbfe3
https://doi.org/10.23937/2469-5858/1510091

The French Gaucher's disease registry: clinical characteristics, complications and treatment of 562 patients

Autor: Christine de Roux-Serratrice, Jérôme Stirnemann, Dries Dobbelaere, Bernard Grosbois, Olivier Fain, Fabrice Camou, Thierry Levade, Agathe Masseau, Vassili Valayanopoulos, Djazia Heraoui, Marc G. Berger, Bruno Fantin, Marie T. Vanier, Cyril Mignot, Linda Rossi-Semerano, Catherine Caillaud, Christian Rose, Nadia Belmatoug, Alain Robert, Frédéric Sedel, Marie Vigan, P. Kaminsky, Thierry Billette de Villemeur, Dalil Hamroun, Roselyne Froissart

Publikováno v: Orphanet Journal of Rare Diseases, Vol. 7 (2012) P. 77
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2012, 7 (1), pp.77. ⟨10.1186/1750-1172-7-77⟩
Orphanet Journal of Rare Diseases, 2012, 7 (1), pp.77. ⟨10.1186/1750-1172-7-77⟩
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 77 (2012)
Orphanet Journal of Rare Diseases, BioMed Central, 2012, 7 (1), pp.77. 〈10.1186/1750-1172-7-77〉

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 GD, livi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c631ddefd5e55795095ec12e5238f0b7
https://archive-ouverte.unige.ch/unige:78658

Esophageal web in Zinsser-Engman-Cole-Fanconi disease

Autor: Patrick Disdier, Jacques Serratrice, Pierre Jean Weiller, Brigitte Granel, Jean-Marc Escoffier, Christine de Roux-Serratrice

Publikováno v: Gastrointestinal endoscopy. 52(4)

Zinsser-Engman-Cole-Fanconi disease (ZECF) or dyskeratosis congenita (DC) is a rare, genetic, X chromosome–linked recessive disorder characterized by skin changes, progressive bone-marrow failure, and a predisposition to develop certain malignancie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea017235615dd31fee83834e4fd84f92
https://pubmed.ncbi.nlm.nih.gov/11023586