Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Human Genetics|December 18, 1998
Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type IbK Ihara, R Kuromaru, T Hara
American Journal of Medical Genetics|May 8, 1999
Rubinstein-Taybi syndrome: a girl with a history of neuroblastoma and premature thelarcheK Ihara, R Kuromaru, M Takemoto, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 10, 2001
Hypothalamic hamartoma associated with an arachnoid cystS Nishio, T Morioka, Y Hamada, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Prevention of hypoglycaemia in a patient with type Ib glycogen storage disease by an amylase (alpha-glucosidase) inhibitorK Ihara, R Kuromaru, A Ryu, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 1, 1996
Body composition, atherogenic risk factors and apolipoproteins following growth hormone treatmentH M Hassan, H Kohno, R Kuromaru, et al.
Endocrine Journal|June 11, 2002
Long-term effect of growth hormone (GH) treatment on body composition in children with GH deficiencyR Kuromaru, H Kohno, N Ueyama, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Long-term prospective study of body composition and lipid profiles during and after growth hormone (GH) treatment in children with GH deficiency: gender-specific metabolic effectsR Kuromaru, H Kohno, N Ueyama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 12, 2001
Association between birthweight and body mass index at 3 years of ageT Tanaka, A Matsuzaki, R Kuromaru, et al.
Journal of Medical Systems|August 1, 1997
A simple WWW interface and quick response system-information query system for cross-sectional body dimensionsE Hanada, Y Kenjo, K Hatae, et al.
European Journal of Pediatrics|September 20, 1997
An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme: a carboxylase deficiency detected by newborn screening for maple syrup urine diseaseK Ihara, R Kuromaru, Y Inoue, et al.
Pageof 2