Chiemi Hayakawa

Nonsense and Frameshift Mutations in ZFHX1B, Encoding Smad-Interacting Protein 1, Cause a Complex Developmental Disorder with a Great Variety of Clinical Features

Kenichiro Yamada, Yasukazu Yamada, Noriko Nomura et al. · The American Journal of Human Genetics · 2001 · 100 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +12

Epilepsy in Angelman Syndrome Associated with Chromosome 15q Deletion

Akiko Matsumoto, Toshiyuki Kumagai, Kiyokuni Miura et al. · Epilepsia · 1992 · 95 citations

Two cases of partial trisomy 21 (pter‐q22.1) without the major features of Down syndrome

Yoko Kondo, Seiji Mizuno, Kei Ohara et al. · American Journal of Medical Genetics Part A · 2006 · 85 citations

Nonketotic hyperglycinemia: Treatment with NMDA antagonist and consideration of neuropathogenesis

Yukihiro Ohya, Nobuhiko Ochi, Naoki Mizutani et al. · Pediatric Neurology · 1991 · 56 citations

Metabolic Syndrome, Neurophysiology, Medicine +8

Guanidino compounds in hyperargininemia.

Naoki Mizutani, Chiemi Hayakawa, Yukihiro Ohya et al. · The Tohoku Journal of Experimental Medicine · 1987 · 42 citations · Full text