Manabu Wakamatsu

Nagoya, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 47 publications

Single-cell RNA sequencing reveals distinct immune interaction networks in primary and reactivated HHV-6B infection.

Single-cell RNA sequencing reveals distinct immune interaction networks in primary and reactivated HHV-6B infection.

Journal: The Journal of infectious diseases

Published: May 13, 2026

Nationwide TREC/KREC-based newborn screening and clinical outcomes in Japan.

Nationwide TREC/KREC-based newborn screening and clinical outcomes in Japan.

Journal: Journal of human immunity

Published: May 04, 2026

Pediatric T-cell lymphoblastic lymphoma with t(9;17)(q34;q23)-associated N-terminally truncated NOTCH1 activation: a case report.

Pediatric T-cell lymphoblastic lymphoma with t(9;17)(q34;q23)-associated N-terminally truncated NOTCH1 activation: a case report.

Journal: International journal of hematology

Published: February 20, 2026

Reticular Dysgenesis in an Extremely Low Birth Weight Infant: A Case Report.

Reticular Dysgenesis in an Extremely Low Birth Weight Infant: A Case Report.

Journal: Journal of clinical immunology

Published: January 13, 2026

Molecular Remission Confirmed by Monitoring a PTPN11 Mutation in Myeloid Leukemia of Down Syndrome Treated With Reduced-Intensity Stem Cell Transplantation: A Case Report.

Molecular Remission Confirmed by Monitoring a PTPN11 Mutation in Myeloid Leukemia of Down Syndrome Treated With Reduced-Intensity Stem Cell Transplantation: A Case Report.

Journal: Pediatric blood & cancer

Published: November 04, 2025

Response to recombinant human granulocyte colony-stimulating factor in reticular dysgenesis.

Response to recombinant human granulocyte colony-stimulating factor in reticular dysgenesis.

Journal: Journal of human immunity

Published: October 26, 2025

Error-corrected next-generation sequencing for profiling the subclonal genetic architecture of juvenile myelomonocytic leukemia.

Error-corrected next-generation sequencing for profiling the subclonal genetic architecture of juvenile myelomonocytic leukemia.

Journal: Leukemia

Published: September 12, 2025

Clinical Spectrum of Noonan Syndrome-Associated Myeloproliferative Disorder.

Clinical Spectrum of Noonan Syndrome-Associated Myeloproliferative Disorder.

Journal: American journal of hematology

Published: July 10, 2025

Allogeneic Hematopoietic Cell Transplantation for Congenital Athymia: A Nationwide Retrospective Study in Japan.

Allogeneic Hematopoietic Cell Transplantation for Congenital Athymia: A Nationwide Retrospective Study in Japan.

Journal: Journal of clinical immunology

Published: June 19, 2025

Dyskeratosis Congenita Complicated by Pulmonary Fibrosis and Myelodysplastic Syndrome with a Germline Mutation of the DKC1 Gene and a Somatic Mutation of the U2AF1 Gene in Leukocytes.

Dyskeratosis Congenita Complicated by Pulmonary Fibrosis and Myelodysplastic Syndrome with a Germline Mutation of the DKC1 Gene and a Somatic Mutation of the U2AF1 Gene in Leukocytes.

Journal: Internal medicine (Tokyo, Japan)

Published: April 06, 2025

Whole-genome sequencing reveals genetic backgrounds in Japanese patients with hemophagocytic lymphohistiocytosis treated with the HLH-2004 protocol.

Whole-genome sequencing reveals genetic backgrounds in Japanese patients with hemophagocytic lymphohistiocytosis treated with the HLH-2004 protocol.

Journal: International journal of hematology

Published: January 22, 2025

Cord Blood Transplantation Using Myeloablative Conditioning for Pediatric Advanced Myelodysplastic Syndrome in AMeD Syndrome With a Novel ADH5 Variant.

Cord Blood Transplantation Using Myeloablative Conditioning for Pediatric Advanced Myelodysplastic Syndrome in AMeD Syndrome With a Novel ADH5 Variant.

Journal: Pediatric blood & cancer

Published: September 27, 2024

Showing 1-12 of 47

Last Updated: 09/26/2026