Mariko Nakacho

Cytochrome P450 Oxidoreductase Deficiency: Identification and Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients

Maki Fukami, Gen Nishimura, Keiko Homma et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 114 citations

Life Sciences, Genetics, Molecular Genetics +17

Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter

Noriyuki Namba, Yuri Etani, Taichi Kitaoka et al. · European Journal of Pediatrics · 2007 · 89 citations

Medicine, Endocrinology, Genetics +16

Efficacy and Safety of Azathioprine and 6-Mercaptopurine in Japanese Pediatric Patients with Ulcerative Colitis: A Survey of the Japanese Society for Pediatric Inflammatory Bowel Disease

Hitoshi Tajiri, Tsuyoshi Tomomasa, Atsushi Yoden et al. · Digestion · 2008 · 28 citations

Medicine, Pediatrics, Pharmacotherapy +15

Cow's milk protein allergy presenting with Hirschsprung's disease–mimicking symptoms

Akio Kubota, Hisayoshi Kawahara, Hiroomi Okuyama et al. · Journal of Pediatric Surgery · 2006 · 19 citations

Life Sciences, Immunology, Pathobiology +10

Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment

Hironori Nagasaka, Haruki Komatsu, Ayano Inui et al. · Molecular Genetics and Metabolism · 2016 · 17 citations

Life Sciences, Biochemistry, Physiology +16