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Human Genetics|July 29, 2000
Statistical and mutational analysis of chronic granulomatous disease in Japan with special reference to gp91-phox and p22-phox deficiencyF Ishibashi, H Nunoi, F Endo, et al.Brain & Development|January 1, 1982
Sural nerve lesions in a case of hypertyrosinemiaY Origuchi, F Endo, A Kitano, et al.Pediatric Research|January 1, 1983
Chemotactic receptor of cord blood granulocytes to the synthesized chemotactic peptide N-formyl-methionyl-leucyl-phenylalanineH Nunoi, F Endo, S Chikazawa, et al.Helvetica Paediatrica Acta|May 1, 1986
Influence of the type of feeding on the presence of PIVKA-II in infantsJ Widdershoven, K Motohara, F Endo, et al.The Journal of Clinical Investigation|July 1, 1987
Altered kinetic properties of the branched-chain alpha-keto acid dehydrogenase complex due to mutation of the beta-subunit of the branched-chain alpha-keto acid decarboxylase (E1) component in lymphoblastoid cells derived from patients with maple syrup urine diseaseY Indo, A Kitano, F Endo, et al.Human Genetics|September 1, 1988
Maple syrup urine disease: a possible biochemical basis for the clinical heterogeneityY Indo, I Akaboshi, Y Nobukuni, et al.Human Molecular Genetics|February 13, 2001
Congenital insensitivity to pain with anhidrosis (CIPA): effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factorS Mardy, Y Miura, F Endo, et al.Pediatrics|July 1, 1989
Relationship of milk intake and vitamin K supplementation to vitamin K status in newbornsK Motohara, I Matsukane, F Endo, et al.Pediatric Research|April 1, 1985
Detection of vitamin K deficiency by use of an enzyme-linked immunosorbent assay for circulating abnormal prothrombinK Motohara, Y Kuroki, H Kan, et al.Pediatric Research|April 1, 1984
Hyperimmunoglobulin-E-associated recurrent infection syndrome accompanied by chemotactic inhibition of polymorphonuclear leukocytes and monocytesS Chikazawa, H Nunoi, F Endo, et al.Pageof 50