Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pascale Trioche, Eberschweiler"'
Autor:
François Petit, Philippe Labrune, Alix Mollet Boudjemline, Pascale Trioche Eberschweiler, Vincent Gajdos, Aurélie Hubert-Buron
Publikováno v:
La Presse Médicale. 37:1172-1177
Hepatic glycogen storage diseases are rare inherited conditions affecting glycogen metabolism. During the last twenty years, medical progress has allowed children who used to die before they reached the age of ten years to reach adulthood. It is impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2713979df0bb71c30025f41c74951f5f
https://doi.org/10.1016/j.lpm.2007.09.023
https://doi.org/10.1016/j.lpm.2007.09.023
Autor:
Pascale Trioche-Eberschweiler, Philippe Labrune, Alix Mollet-Boudjemline, David Fallik, Laurence Weiss, Laurence Foix-L’Helias
Publikováno v:
Acta Paediatrica. 94:1158-1161
UNLABELLED An adolescent was hospitalized for recurring abdominal pains, which had previously led to appendicectomy. Laboratory data finally led to the diagnosis of hereditary angioneurotic oedema, after several hypotheses had been raised and ruled o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3597d345cae50087b61074a3b608249
https://doi.org/10.1111/j.1651-2227.2005.tb02064.x
https://doi.org/10.1111/j.1651-2227.2005.tb02064.x
Autor:
François Petit, Pascale Trioche Eberschweiler, Alix Mollet Boudjemline, Christine Vianey-Saban, Monique Piraud, Roseline Froissart, Philippe Labrune, Vincent Gajdos, Aurélie Hubert-Buron
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2011, 6 (1), pp.27. ⟨10.1186/1750-1172-6-27⟩
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 27 (2011)
Orphanet Journal of Rare Diseases, BioMed Central, 2011, 6 (1), pp.27. ⟨10.1186/1750-1172-6-27⟩
Orphanet Journal of Rare Diseases, Vol 6, Iss 1, p 27 (2011)
Glucose-6-phosphatase deficiency (G6P deficiency), or glycogen storage disease type I (GSDI), is a group of inherited metabolic diseases, including types Ia and Ib, characterized by poor tolerance to fasting, growth retardation and hepatomegaly resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e0f15c2fe3c29e5b28c1542b8bbd8ee
https://doi.org/10.1186/1750-1172-6-27
https://doi.org/10.1186/1750-1172-6-27
Autor:
Philippe, Labrune, Pascale Trioche, Eberschweiler, Alix Mollet, Boudjemline, Aurélie, Hubert-Buron, François, Petit, Vincent, Gajdos
Publikováno v:
Presse medicale (Paris, France : 1983). 37(7-8)
Hepatic glycogen storage diseases are rare inherited conditions affecting glycogen metabolism. During the last twenty years, medical progress has allowed children who used to die before they reached the age of ten years to reach adulthood. It is impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::445228fb88c195d490e4849339ba9f7f
https://pubmed.ncbi.nlm.nih.gov/18313893
https://pubmed.ncbi.nlm.nih.gov/18313893
Autor:
Laurence, Foix-L'Hélias, Laurence, Weiss, Alix, Mollet-Boudjemline, David, Fallik, Pascale, Trioche-Eberschweiler, Philippe, Labrune
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 94(8)
An adolescent was hospitalized for recurring abdominal pains, which had previously led to appendicectomy. Laboratory data finally led to the diagnosis of hereditary angioneurotic oedema, after several hypotheses had been raised and ruled out.Angioneu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7aaf780caaaa66c6f005d48382edccd
https://pubmed.ncbi.nlm.nih.gov/16188868
https://pubmed.ncbi.nlm.nih.gov/16188868