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Publications by Naruo Kuwashima

A Case of Allgrove Syndrome With a Novel IVS7 +1 G>A Mutation of the AAAS Gene

Clinical Pediatric Endocrinology

English

Delivery of Interferon-Α Transfected Dendritic Cells Into Central Nervous System Tumors Enhances the Antitumor Efficacy of Peripheral Peptide-Based Vaccines

Cancer Research

Oncology

2004

English

Related publications

Novel Mutation in the AAAS Gene in a Severely Affected Triple-A Syndrome Patient

Endocrinology & Metabolic Syndrome

2015

English

A Novel Gene Mutation in Berardinelli Seip Syndrome: Three Case Reports

Endocrine Abstracts

2016

English

A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1

Annals of Pediatric Endocrinology and Metabolism

English

Administration of Anesthesia in a Patient With Allgrove Syndrome

Case Reports in Anesthesiology

2012

English

A Novel ROGDI Gene Mutation Is Associated With Kohlschutter-Tonz Syndrome

Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

English

A Neonatal Case of HDR Syndrome and a Vascular Ring With a Novel GATA3 Mutation

Human Genome Variation

English

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

Frontiers in Genetics

Genetics

Molecular Medicine

2018

English

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in Pediatrics

English

A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)

Tohoku Journal of Experimental Medicine

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Naruo Kuwashima

A Case of Allgrove Syndrome With a Novel IVS7 +1 G>A Mutation of the AAAS Gene

Delivery of Interferon-Α Transfected Dendritic Cells Into Central Nervous System Tumors Enhances the Antitumor Efficacy of Peripheral Peptide-Based Vaccines

Related publications

Novel Mutation in the AAAS Gene in a Severely Affected Triple-A Syndrome Patient

A Novel Gene Mutation in Berardinelli Seip Syndrome: Three Case Reports

A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1

Administration of Anesthesia in a Patient With Allgrove Syndrome

A Novel ROGDI Gene Mutation Is Associated With Kohlschutter-Tonz Syndrome

A Neonatal Case of HDR Syndrome and a Vascular Ring With a Novel GATA3 Mutation

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)