Hiroyasu Nakagawa

Reply to: Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1

Y. Niida, M. Kuroda, Y. Mitani, 2017, Brain and Development.

A girl with infantile neuronal ceroid lipofuscinosis caused by novel PPT1 mutation and paternal uniparental isodisomy of chromosome 1

Y. Niida, M. Kuroda, Y. Mitani, 2016, Brain and Development.

Serum tau protein as a marker of disease activity in enterohemorrhagic Escherichia coli O111-induced hemolytic uremic syndrome

H. Kanegane, Mika Ito, Y. Niida, 2015, Neurochemistry International.

A Say‐Barber‐Biesecker‐Young‐Simpson variant of Ohdo syndrome with a KAT6B 10‐base pair palindromic duplication: A recurrent mutation causing a severe phenotype mixed with genitopatellar syndrome

Y. Niida, M. Kuroda, Y. Mitani, 2017, Congenital anomalies.

Flow cytometric analysis of skin blister fluid induced by mosquito bites in a patient with chronic active Epstein–Barr virus infection

T. Wada, A. Yachie, M. Shimizu, 2009, International journal of hematology.

Title Flow cytometric analysis of skin blister fluid induced by mosquito bites ina patient with chronic active Epstein-Barr virus infection

T. Wada, A. Yachie, M. Shimizu, 2017 .

Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome.

Y. Hasegawa, T. Tajima, K. Nagasaki, 2011, Endocrine journal.