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Journal of Human Genetics|June 11, 1998
Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complexM Tsuruta, H Mitsubuchi, S Mardy, et al.
Internal Medicine (Tokyo, Japan)|November 1, 1995
Occurrence of Graves' disease during retreatment with interferon-alpha 2a for chronic hepatitis CM Wada, W Hiraizumi, M Fujimoto, et al.
Pediatric Research|July 1, 1997
The effect of carnitine on ketogenesis in perfused livers from juvenile visceral steatosis mice with systemic carnitine deficiencyT Nakajima, M Horiuchi, H Yamanaka, et al.
The American Journal of Gastroenterology|November 1, 1994
Simultaneous occurrence of adenomas in stomach, duodenal bulb, and colon: disappearance of gastric and duodenal adenomas during oral administration of 5'-deoxy-5-fluorouridineM Wada, H Jin, A Kinugasa, et al.
Pediatric Research|May 1, 1984
Enzyme defect in a case of tyrosinemia type I, acute formN Furukawa, A Kinugasa, T Seo, et al.
Acta Paediatrica Scandinavica|January 1, 1991
Alloimmune neonatal neutropenia in monozygous twins. High-dose intravenous gammaglobulin therapyN Yoshida, T Shikata, S Sudo, et al.
Pediatric Diabetes|March 16, 2004
The Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT): initial aims and impact of the family history of type 1 diabetes mellitus in Japanese childrenN Matsuura, Y Yokota, K Kazahari, et al.
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