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Cell Transplantation|September 18, 2015
Optimization and Scale-up Isolation and Culture of Neonatal Porcine Islets: Potential for Clinical ApplicationCara Ellis, James G Lyon, Gregory S KorbuttArchives Francaises De Pediatrie|March 1, 1977
[Schilder's disease with adrenal insufficiency (adreno-leukodystrophy). Apropos of 5 cases]M O Livet, J L Chaussain, G LyonInternational Archives of Allergy and Applied Immunology|January 1, 1991
Alpha-2-macroglobulin-kallikrein complex: a temperature-sensitive mediator in contact-system-induced inflammation with a potential role in late and delayed hypersensitivity responsesE C Lasser, S G Lyon, S NegreteThe Pediatric Infectious Disease Journal|October 1, 1996
Serum alpha-interferon in lower respiratory tract infections of childrenF Moulin, J Raymond, J L Iniguez, et al.The Journal of Infectious Diseases|September 1, 1992
Absence of intrathecal synthesis of some interferon-alpha subtypes in bacterial meningitisJ Raymond, C Benichou, D de Boissieu, et al.Acta Paediatrica (Oslo, Norway : 1992)|August 12, 2004
Aicardi-Goutières syndrome: clinical and neuroradiological findings of 10 new casesG M H Abdel-Salam, M S Zaki, P Lebon, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]J M Pinard, C Marsac, E Barkaoui, et al.Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.Archives Francaises De Pediatrie|November 1, 1983
[Nosological aspects of epilepsia partialis continua in children]O Dulac, C Dravet, P Plouin, et al.Journal of Inherited Metabolic Disease|November 20, 1998
Diffuse leukodystrophy in an infant with cytochrome-c oxidase deficiencyJ P Harpey, D Heron, M Prudent, et al.Pageof 39