Showing results (171-180 of 381) with videos related to
Sort By:
Pageof 39
International 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 NegreteThrombosis and Haemostasis|October 28, 1987
Modification of an amidolytic heparin assay to express protein-bound heparin and to correct for the effect of antithrombin III concentrationS G Lyon, E C Lasser, R SteinCell 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 KorbuttThe 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