Go Tajima

Newborn screening for Fabry disease in the western region of Japan

Takaaki Sawada, Jun Kido, Shinichiro Yoshida et al. · Molecular Genetics and Metabolism Reports · 2020 · 67 citations · Full text

Effects of idursulfase enzyme replacement therapy for Mucopolysaccharidosis type II when started in early infancy: Comparison in two siblings

Go Tajima, Nobuo Sakura, Motomichi Kosuga et al. · Molecular Genetics and Metabolism · 2013 · 62 citations

Inherited Metabolic Disease, Pediatrics, Pathology +4

Useful second‐tier tests in expanded newborn screening of isovaleric acidemia and methylmalonic aciduria

Yosuke Shigematsu, Ikue Hata, Go Tajima · Journal of Inherited Metabolic Disease · 2010 · 49 citations

Differential diagnosis of neonatal mild hypergalactosaemia detected by mass screening: Clinical significance of portal vein imaging

Yutaka Nishimura, Go Tajima, Andi Dwi Bahagia et al. · Journal of Inherited Metabolic Disease · 2004 · 48 citations

Different neuroradiological findings during two stroke-like episodes in a patient with a congenital disorder of glycosylation type Ia

Nobutsune Ishikawa, Go Tajima, Hiroaki Ono et al. · Brain and Development · 2008 · 37 citations

Stroke-like Episodes, Neurological Disorder, Medicine +8