Yu Tsuyusaki

Molecular genetic analysis of 30 families with Joubert syndrome

Toshifumi Suzuki, Noriko Miyake, Yoshinori Tsurusaki et al. · Clinical Genetics · 2016 · 56 citations

Rare Diseases, Developmental Biology, Mendelian Disorder +11

Expansion of the phenotype of Kosaki overgrowth syndrome

Mari Minatogawa, Toshiki Takenouchi, Yu Tsuyusaki et al. · American Journal of Medical Genetics Part A · 2017 · 39 citations

Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness

Hitoshi Osaka, Atsushi Takagi, Yu Tsuyusaki et al. · Molecular Genetics and Metabolism · 2012 · 37 citations

Neurobiology Of Disease, Severe Dystonia, Corticobasal Degeneration +11

1p36 deletion syndrome associated with Prader–Willi‐like phenotype

Yu Tsuyusaki, Hiroshi Yoshihashi, Noritaka Furuya et al. · Pediatrics International · 2010 · 31 citations

Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia

Yu Tsuyusaki, Hiroko Shimbo, Takahito Wada et al. · Brain and Development · 2011 · 27 citations

Electrolyte Disorder, Neurophysiology, Physiology +5