K. Kitamura

Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia

S. Miyano, Y. Shiraishi, S. Ogawa, 2015, Journal of thrombosis and haemostasis : JTH.

Diagnostic biomarker for ACTN1 macrothrombocytopenia.

M. Yasutomi, S. Kunishima, R. Kobayashi, 2015, Blood.

Normal neutrophil myosin IIA localization in an immunofluorescence analysis can rule out MYH9 disorders

S. Miyano, Y. Shiraishi, K. Chiba, 2013, Journal of thrombosis and haemostasis : JTH.

Somatic mosaicism in MYH9 disorders: the need to carefully evaluate apparently healthy parents

H. Saito, S. Kunishima, T. Sekine, 2014, British journal of haematology.

Transient hemiparesis in a 14-year-old boy with MYH9 disorders

M. Kubota, S. Kunishima, S. Kumaki, 2012, International Journal of Hematology.

A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia

O. Ohara, S. Saitoh, S. Kunishima, 2018, Brain and Development.

The first two cases of MYH9 disorders in Thailand: an international collaborative study

S. Kunishima, S. Hongeng, T. Sekine, 2015, Annals of Hematology.