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Neuroradiology|April 17, 1999
High-intensity basal ganglia lesions on T1-weighted images in two toddlers with elevated blood manganese with portosystemic shuntsK Ihara, T Hijii, R Kuromaru, et al.Acta Geneticae Medicae Et Gemellologiae|January 1, 1992
Monozygotic twins with discordant sexK Kurosawa, R Kuromaru, K Imaizumi, et al.Clinical Endocrinology|June 6, 2007
The Leu544Ile polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiencyK Ihara, M Inuo, R Kuromaru, et al.Journal of Inherited Metabolic Disease|September 10, 2005
A case of hyperinsulinism/hyperammonaemia syndrome with reduced carbamoyl-phosphate synthetase-1 activity in liver: a pitfall in enzymatic diagnosis for hyperammonaemiaK Ihara, K Miyako, M Ishimura, et al.Genes and Immunity|April 18, 2002
Association study between CD30 and CD30 ligand genes and type 1 diabetes in the Japanese populationS Ahmed, K Ihara, W M Bassuny, et al.Immunogenetics|October 31, 2001
Association studies of CTLA-4, CD28, and ICOS gene polymorphisms with type 1 diabetes in the Japanese populationK Ihara, S Ahmed, F Nakao, et al.Human Genetics|February 1, 1997
The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patientsA Nishiyori, M Yoshino, H Kato, et al.Pageof 2