H. Watanabe

Treatment with OK-432 for persistent congenital chylothorax in newborn infants resistant to octreotide

Eiji Matsukuma, Yusuke Aoki, Miho Sakai et al. · Journal of Pediatric Surgery · 2009 · 40 citations

Newborn Infants, Pneumothorax, Pediatrics +7

A new Japanese case of succinyl‐CoA: 3‐ketoacid CoA‐transferase deficiency

Hiromi Sakazaki, Kyosuke Hirayama, SATOMI MURAKAMI et al. · Journal of Inherited Metabolic Disease · 1994 · 35 citations

Biochemistry, Genetic Disorder, New Japanese Case +4

Myopathic Form of Very-Long Chain Acyl-CoA Dehydrogenase Deficiency: Evidence for Temperature-Sensitive Mild Mutations in Both Mutant Alleles in a Japanese Girl

Toshiyuki Fukao, H. Watanabe, Kenji E. Orii et al. · Pediatric Research · 2001 · 33 citations · Full text

Biology, Mendelian Disorder, Genetic Disorder +11

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: Two pathogenic mutations, V133E and C456F, in Japanese siblings

Xiang‐Qian Song, Toshiyuki Fukao, H. Watanabe et al. · Human Mutation · 1998 · 25 citations

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency

Xiang‐Qian Song, Toshiyuki Fukao, Grant A. Mitchell et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1997 · 25 citations

Autoimmune Disease, Genetic Disorder, Genetics +9