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

Medicine, Endocrinology, Pediatrics +16

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

Life Sciences, Genetics, Molecular Genetics +17

Hereditary ceruloplasmin deficiency with hemosiderosis

Nobuhiko Okamoto, Shun‐ichi Wada, Toru Oga et al. · Human Genetics · 1996 · 105 citations

Medicine, Genetics, Pathology +9

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 · 104 citations

Medicine, Neurobiology, Neuroscience +16

A new case of UDP‐galactose transporter deficiency (SLC35A2‐CDG): molecular basis, clinical phenotype, and therapeutic approach

K Dörre, Mariusz Olczak, Yoshiro Wada et al. · Journal of Inherited Metabolic Disease · 2015 · 87 citations

Life Sciences, Molecular Biology, Molecular Genetics +15