Y. Shimizu

发表

Chromosomal aberration in lipoblastoma: a case with 46,XX,ins(8;6)(q11.2;q13q27).

T. Shiihara, K. Hayasaka, E. Saitoh, 1997, Cancer genetics and cytogenetics.

CD48 expression on leukocytes in infectious diseases: Flow cytometric analysis of surface antigen

K. Hayasaka, T. Mitsui, Y. Shimizu, 1998, Acta paediatrica Japonica : Overseas edition.

Successful unrelated donor bone marrow transplantation for shwachman-diamond syndrome with leukemia

K. Hayasaka, T. Mitsui, Y. Shimizu, 2004, International journal of hematology.

Novel breakpoints of the EWS gene and the WT1 gene in a desmoplastic small round cell tumor.

K. Hayasaka, K. Hayasaka, T. Mitsui, 1998, Cancer genetics and cytogenetics.

Severe Bleeding Tendency in a Patient With Bernard‐Soulier Syndrome Associated With a Homozygous Single Base Pair Deletion in the Gene Coding for the Human Platelet Glycoprotein Ibα

Tomohiro Hayashi, K. Hayasaka, T. Hayashi, 1998, Journal of pediatric hematology/oncology.

Mild Bleeding Disorder: Deficiency of the lnositol 1,4,5-Triphosphate Formation despite Normal G-protein Activation

K. Hayasaka, T. Mitsui, Y. Shimizu, 2018 .

Defective Signal Transduction through the Thromboxane A2 Receptor in a Patient with a Miid Bleeding Disorder: Deficiency of the Inositol 1,4,5-Triphosphate Formation despite Normal G-protein Activation

K. Hayasaka, T. Mitsui, Y. Shimizu, 1997, Thrombosis and Haemostasis.

Intermittent jaundice in patients with acute leukaemia: A common mutation of the bilirubin uridine-diphosphate glucuronosyltransferase gene among Asians

K. Hayasaka, C. Lin, K. Akaba, 1999, Journal of Inherited Metabolic Disease.

A Case of Acral Erythema Induced by Conditioning Regimen of Bone Marrow Transplantation

K. Hayasaka, T. Mitsui, Y. Shimizu, 1995 .

Multiple sulphatase deficiency and haemophagocytic syndrome

K. Hayasaka, Y. Shimizu, M. Kato, 1998, European Journal of Pediatrics.