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Pediatric Dermatology|September 1, 1994
Sweet syndrome as the presenting manifestation of chronic granulomatous disease in an infantD Sedel, P Huguet, C Lebbe, et al.Archives Francaises De Pediatrie|March 1, 1990
[Sclerosing cholangitis revealing histiocytosis X]I Neveu, P Labrune, P Huguet, et al.Pediatric Cardiology|July 1, 1991
Cardiomyopathy in glycogen-storage disease type III: clinical and echographic study of 18 patientsP Labrune, P Huguet, M OdievreJournal of Inherited Metabolic Disease|January 1, 1992
In vivo 13C-NMR evaluation of glycogen content in a patient with glycogen storage diseaseP Labrune, P Jehenson, A Syrota, et al.Journal of Medical Genetics|August 1, 1992
Progressive vitiligo, mental retardation, facial dysmorphism, and urethral duplication without chromosomal breakage or immunodeficiencyP Labrune, R Assathiany, D Penso, et al.Archives Francaises De Pediatrie|November 1, 1988
[Long-term course of hepatic glycogenosis. A retrospective study of 76 cases]L de Parscau, P Guibaud, P Labrune, et al.Journal of Inherited Metabolic Disease|October 13, 2001
Partial effect of bromocriptine on lactose and galactose synthesis in a pregnant woman heterozygous for galactosaemiaM Odièvre, M Brivet, M F Rivière, et al.Archives Francaises De Pediatrie|November 1, 1989
[Intermittent intracranial hypertension revealing a tumor of the cervical spine]V Toulemonde, P Labrune, C Sainte Rose, et al.Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1995
Failure of cefotaxime treatment in two children with meningitis caused by highly penicillin-resistant Streptococcus pneumoniaeM Guibert, H Chahime, J Petit, et al.Journal of Pediatric Gastroenterology and Nutrition|March 1, 1997
Hepatocellular adenomas in glycogen storage disease type I and III: a series of 43 patients and review of the literatureP Labrune, P Trioche, I Duvaltier, et al.Pageof 18