Atsushi Sakamoto

9PUBLICATIONS
16CO-AUTHORS
Infant and child healthCardiology (incl. cardiovascular diseases)Anthropological geneticsDevelopmental genetics (incl. sex determination)Respiratory diseases
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Publications (9)

|Aug 27, 2026
Long-Term Restoration of Anticoagulant Function After Liver Transplantation for Severe Congenital Protein C Deficiency: A Single-Center Experience Involving Three Pediatric Patients.

|Dec 27, 2025
CYCS-related thrombocytopenia in three Japanese families with a novel variant in one family.

Natsuhiko Yamada, Atsushi Sakamoto, Rintaro Nagoshi

|Sep 15, 2025
Differential transcript level of ANKRD26 and clinical phenotype among the ANKRD26 variants in the Japanese registry for congenital thrombocytopenia.

Atsushi Sakamoto, Toru Uchiyama, Kazuhiko Nakabayashi

|Sep 04, 2024
Platelet changes and bleeding symptoms in children, adolescents, and adults with 22q11.2 deletion syndrome.

Atsushi Sakamoto, Toru Uchiyama, Ryohei Futatsugi

|Apr 23, 2024
Diagnostic delay of MYH9-related disorder in Japan.

Atsushi Sakamoto, Toru Uchiyama, Tadashi Kaname

|Apr 16, 2024
Bernard-Soulier syndrome caused by a novel GP1BB variant and 22q11.2 deletion.

Rintaro Nagoshi, Atsushi Sakamoto, Tsuyoshi Imai

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Frequent Collaborators

4 joint publications

Akira Ishiguro

1 joint publications

Natsuhiko Yamada

1 joint publications

Rintaro Nagoshi

1 joint publications

Saori Endo