Hisakazu Nakajima

7PUBLICATIONS
4CO-AUTHORS
Genetic immunologyMajor global burdens of diseaseInfant and child healthGene and molecular therapyCancer genetics
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Publications (7)

|Apr 09, 2026
A case of Alström syndrome with growth hormone deficiency and dyslipidemia: a novel homozygous frameshift variant of ALMS1 c.5763del.

Takeshi Goda, Hisakazu Nakajima, Yasuhiro Kawabe

|Feb 14, 2022
A Case of Infantile Alagille Syndrome With Severe Dyslipidemia: New Insight into Lipid Metabolism and Therapeutics.

Hisakazu Nakajima, Yusuke Tsuma, Shota Fukuhara

|Oct 15, 2021
Two Japanese siblings with arginase-1 deficiency identified using a novel frameshift mutation of ARG1 (p.Lys41Thrfs∗2).

Hisakazu Nakajima, Shota Fukuhara

|Mar 27, 2019
A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6.

Takeshi Goda, Hiroshi Komatsu, Kandai Nozu

|Jan 05, 2019
High-fat diet accelerates extreme obesity with hyperphagia in female heterozygous Mecp2-null mice.

Shota Fukuhara, Hisakazu Nakajima, Satoru Sugimoto

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