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Takahiro Hamada

Kurume University School of Medicine

H指数:33

被引数:5,971

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KRT10-nEDD-superficial: a novel phenotype characterized by vesicles and skin peeling

KRT10-nEDD-superficial：一种以水疱和皮肤脱屑为特征的新型表型

Journal of Dermatological Science

IF4

2026-05-230

PRE

Susceptibility to Dermatophytosis in SDR9C7-Nonsyndromic Epidermal Differentiation Disorder: Observation of Cutaneous Inflammation Involving IRF4 and IL-17

SDR9C7非综合征性表皮分化障碍中皮肤癣菌病的易感性：涉及IRF4和IL-17的皮肤炎症观察

The Journal of Dermatology

IF0

2025-11-110

PRE

Eccrine syringofibroadenoma as a manifestation of ichthyosis follicularis-atrichia-photophobia syndrome-1

INTERNATIONAL JOURNAL OF DERMATOLOGY

IF3.2

2024-07-110

PRE

Mosaicism for ATP2A2 Mutation and Mutant Allelic Fractions Detected by Droplet Digital PCR in Simple Segmental Darier Disease

ACTA DERMATO-VENEREOLOGICA

IF3.7

2023-07-131

OAAI

Life-long Skin Eruptions along Blaschko's Lines in a 27-year-old Woman: A Quiz

ACTA DERMATO-VENEREOLOGICA

IF3.7

2021-12-070

OAAI

A Novel Microduplication Spanning Exons 8-16 of ATP2C1 That Was Undetectable by Standard Sanger Sequencing in a Japanese Patient With Hailey-Hailey Disease

FRONTIERS IN MEDICINE

IF3

2020-09-042

OAAI

In vivoandin vitroevidence for the inhibition of homogentisate solanesyltransferase by cyclopyrimorate

PEST MANAGEMENT SCIENCE

IF3.8

2019-12-2411

PREAI

Identification of novel and recurrent AAGAB mutations in two patients with punctate palmoplantar keratoderma

JOURNAL OF INVESTIGATIVE DERMATOLOGY

IF5.7

2018-05-010

OAAI

Speckled lentiginous naevus: understanding the process of development and regression

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2018-04-170

PREAI

Prevalence of filaggrin gene mutations in patients with atopic dermatitis and ichthyosis vulgaris in Kyushu area of Japan and South Korea

JOURNAL OF DERMATOLOGICAL SCIENCE

IF4

2017-05-019

PREAI

Detection of SERPINB7 mutation can distinguish Nagashima- type palmoplantar keratoderma from other keratodermas with palmoplantar lesions

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2017-02-164

PREAI

Ce 4f electronic states of CeO1-xFxBiS2 studied by soft x-ray photoemission spectroscopy

PHYSICAL REVIEW B

IF3.7

2017-02-076

PREAI

Functional study of TGM1 missense mutations in autosomal recessive congenital ichthyosis

EXPERIMENTAL DERMATOLOGY

IF3.1

2016-06-152

OAAI

A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome

EXPERIMENTAL DERMATOLOGY

IF3.1

2016-05-209

OAAI

A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases

JOURNAL OF DERMATOLOGICAL SCIENCE

IF4

2016-05-016

PREAI

Two novel missense mutations of STS gene underlie X-linked recessive ichthyosis: understanding of the mutational and structural spectrum

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

IF8

2015-09-215

PREAI

A three-dimensional in vitro culture model of Hailey-Hailey disease

Hailey-hailey病的三维体外培养模型

EXPERIMENTAL DERMATOLOGY

IF3.1

2015-08-183

OAAI

Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia (vol 78, pg 82, 2015)

JOURNAL OF DERMATOLOGICAL SCIENCE

IF4

2015-08-010

PREAI

Desmocollin-specific antibodies in a patient with Hailey-Hailey disease

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2015-05-184

PREAI

Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

JOURNAL OF DERMATOLOGICAL SCIENCE

IF4

2015-04-017

PREAI