Yoshiro Wada

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder

Songya Pang, A. Campbell Clark, Eurico Camargo Neto et al. · Screening · 1993 · 161 citations

Developmental Anomaly, Adrenal Gland, Urology +9

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

Takayuki Ozawa, Masashi Tanaka, Hidekazu Ino et al. · Biochemical and Biophysical Research Communications · 1991 · 122 citations

Mitochondrial Myopathy, Mendelian Disorder, Point Mutations +9

Hereditary ceruloplasmin deficiency with hemosiderosis

Nobuhiko Okamoto, Shun‐ichi Wada, Toru Oga et al. · Human Genetics · 1996 · 104 citations

Down Syndrome, Genetic Disorder, Hematology +6

Vulnerability to Cerebral Hypoxic-Ischemic Insult in Neonatal but Not in Adult Rats Is in Parallel With Disruption of the Blood-Brain Barrier

Kanji Muramatsu, Atsuo Fukuda, Hajime Togari et al. · Stroke · 1997 · 101 citations

Cloning of the human erythropoietin receptor gene

CT Noguchi, KS Bae, Kazuo Chin et al. · Blood · 1991 · 86 citations · Full text