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Annals of the Rheumatic Diseases|August 7, 2004
Scoring of radiographic progression in randomised clinical trials in ankylosing spondylitis: a preference for paired reading orderA Wanders, R Landewé, A Spoorenberg, et al.Pediatrics|September 5, 2006
Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levelsMichaela Liebig, Ina Schymik, Martina Mueller, et al.Human Mutation|May 2, 2000
Molecular basis of very long chain acyl-CoA dehydrogenase deficiency in three Israeli patients: identification of a complex mutant allele with P65L and K247Q mutations, the former being an exonic mutation causing exon 3 skippingH Watanabe, K E Orii, T Fukao, et al.Saudi Medical Journal|December 18, 2001
Carnitine palmityl transferase I deficiencyA I Al-Aqeel, M S Rashed, J P Ruiter, et al.European Journal of Cancer (Oxford, England : 1990)|August 31, 2001
UFT and leucovorin in first-line chemotherapy for patients with metastatic gastric cancer. An Early Clinical Studies Group (ECSG)/European Organization for Research Treatment of Cancer (EORTC) phase II trialA Ravaud, M Borner, J H Schellens, et al.Tumori|May 3, 2011
Serum beta-HCG and CA-125 as tumor markers in a patient with osteosarcoma: case reportDavid S Boss, Hilary Glen, Jos H Beijnen, et al.Transplant International : Official Journal of the European Society for Organ Transplantation|June 24, 2011
Prompt reversal of a severe complement activation by eculizumab in a patient undergoing intentional ABO-incompatible pancreas and kidney transplantationAli-Reza Biglarnia, Bo Nilsson, Thomas Nilsson, et al.Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assemblyY Matsuzono, N Kinoshita, S Tamura, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 29, 1999
Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: clinical, biochemical, and pathological studies on three subjects with this recently identified disorder of mitochondrial beta-oxidationM J Bennett, S D Spotswood, K F Ross, et al.Journal of Inherited Metabolic Disease|January 1, 1992
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defectR J Wanders, C W van Roermund, W Lageweg, et al.Pageof 133