Hidetaka Niizuma

Assistant Professor

Tohoku University Hospital

Japan

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About

Hidetaka Niizuma is an Assistant Professor at Tohoku University Hospital in Japan. His research focuses on the efficacy of rituximab in autoimmunity, clinical decision-making in genomic profiling, and treatment responses in pediatric tumors. He has published articles on topics including the management of germline variants, the effectiveness of reduced-intensity conditioning for stem cell transplantation, and the identification of novel mutations in genetic syndromes.

Articles (11)

Year:

2024

Year:

2023

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2023

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2023

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2023

Year:

2023

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2022

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2022

Year:

2022

Year:

2022

Year:

2021

Collaborators (7)

Hiroyuki Shibata

Professor

Akita University

JAPAN

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Rumi Hachiya

Keio University School of Medicine

JAPAN

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Tsuyoshi Saito

JAPAN

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Yoji Sasahara

JAPAN

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Atsuo Kikuchi

Tohoku University graduate school of medicine

JAPAN

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Takeshi Hiyama

教授 / Professor

Tottori University

JAPAN

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Hiroshi Tada

Associate Professor

Tohoku University

JAPAN

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Hidetaka Niizuma

Research Interests

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Articles (11)

Efficacy of rituximab for the treatment and prevention of autoimmunity in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia

Clinical decisions by the molecular tumor board on comprehensive genomic profiling tests in Japan: A retrospective observational study

Two‐year crizotinib monotherapy induced durable complete response of pediatric ALK‐positive inflammatory myofibroblastic tumor

Comprehensive genomic profiling suggested multifocal development of retinoblastoma in a single eye

Management of patients with presumed germline pathogenic variant from tumor-only genomic sequencing: A retrospective analysis at a single facility

Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome

Identification of clinical factors related to antibody-mediated immune response to the subfornical organ

Clofarabine monotherapy in two patients with refractory Langerhans cell histiocytosis

Living Donor Lobar Lung Transplant for a Patient With Lung Disease Caused by ABCA3 Gene Mutations: A Case Report

Novel POLE mutations identified in patients with IMAGE-I syndrome cause aberrant subcellular localisation and protein degradation in the nucleus

Catecholamine‐induced paralytic ileus controlled by phentolamine in a child with giant differentiating neuroblastoma

Collaborators (7)

Hiroyuki Shibata

Rumi Hachiya

Tsuyoshi Saito

Yoji Sasahara

Atsuo Kikuchi

Takeshi Hiyama

Hiroshi Tada

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