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Journal of Inherited Metabolic Disease|April 5, 2001
Congenital porto-left renal venous shunt as a cause of galactosaemiaN Mizoguchi, N Sakura, H Ono, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|June 12, 1999
Transient galactosemia detected by neonatal mass screeningH Ono, H Mawatari, N Mizoguchi, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|March 7, 2000
Delay of liver maturation as a cause of transient neonatal galactosemiaH Ono, H Mawatari, N Mizoguchi, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|November 21, 1998
Reversed-phase high-performance liquid chromatographic assay method for quantitating 6-mercaptopurine and its methylated and non-methylated metabolites in a single sampleH Mawatari, Y Kato, S Nishimura, et al.Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|January 5, 2000
Disodium cromoglycate use in children and adolescents with asthma: correlation between plasma concentrations and protective effects for various inhalation methodsY Kato, K Muraki, M Fujitaka, et al.British Journal of Clinical Pharmacology|July 27, 1999
Plasma concentrations of disodium cromoglycate after various inhalation methods in healthy subjectsY Kato, K Muraki, M Fujitaka, et al.The Journal of Clinical Investigation|March 1, 1988
Defect in biosynthesis of mitochondrial acetoacetyl-coenzyme A thiolase in cultured fibroblasts from a boy with 3-ketothiolase deficiencyS Yamaguchi, T Orii, N Sakura, et al.Acta Paediatrica Scandinavica|June 1, 1991
Asthma as the first presenting symptom of complex glycerol kinase deficiencyN Sakura, S Nishimura, N Kawahara, et al.Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|April 6, 2001
Significance of the eosinophil cationic protein/eosinophil count ratio in asthmatic patients: its relationship to disease severityM Fujitaka, H Kawaguchi, Y Kato, et al.The Tohoku Journal of Experimental Medicine|June 1, 1992
Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiencyS Yamaguchi, T Fukao, M Kano, et al.Pageof 349