List of works - Ken Okamura

A 4-bp deletion promoter variant (rs984225803) is associated with mild OCA4 among Japanese patients

scientific article published on 31 July 2018

A case of xeroderma pigmentosum complementation group C with diverse clinical features.

scientific article published on 12 January 2018

Case of anti-p200 pemphigoid accompanying uterine malignancy

scientific article published on 15 May 2018

Case of phaeohyphomycosis caused by Cladophialophora boppii successfully treated with local hyperthermia and systemic terbinafine

scientific article published on 24 April 2020

Characterization of melanosomes and melanin in Japanese patients with Hermansky-Pudlak syndrome types 1, 4, 6, and 9.

scientific article

Clinical and immunological characterization of 14 cases of dipeptidyl peptidase-4 inhibitor-associated bullous pemphigoid: a single-centre study

scientific article published on 24 November 2019

Current landscape of Oculocutaneous Albinism in Japan

scientific article published on 24 September 2020

Expression of discoidin domain receptor 1 and E-cadherin in epidermis affects melanocyte behavior in rhododendrol-induced leukoderma mouse model

scientific article published on 08 August 2020

Five novel mutations in SASH1 contribute to lentiginous phenotypes in Japanese families

scientific article published on 27 September 2020

Genome-wide association study identifies CDH13 as a susceptibility gene for rhododendrol-induced leukoderma

scientific article published on 18 June 2020

Identification of two novel mutations in a Japanese patient with Hermansky-Pudlak syndrome type 5

scientific article published on 02 September 2020

Impact of a 4-bp deletion variant (rs984225803) in the promoter region of SLC45A2 on color variation among a Japanese population

scientific article published on 27 February 2019

Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mouse model of rhododendrol-induced vitiligo

scientific article published on 10 April 2019

NGS-based targeted resequencing identified rare subtypes of albinism: Providing accurate molecular diagnosis for Japanese patients with albinism

scientific article published on 09 June 2019

Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in KRT5

scientific article published on 28 January 2019

Neutrophilic dermatosis associated with an NFKB2 mutation

scientific article published on 28 September 2018

Novel AP3B1 compound heterozygous mutations in a Japanese patient with Hermansky-Pudlak syndrome type 2

scientific article published on 09 December 2019

Paradoxical exacerbation of latent interstitial pneumonia by secukinumab in a patient with psoriasis vulgaris

scientific article published on 01 January 2019

Report of two Japanese patients with piebaldism including a novel mutation in KIT

scientific article published on 06 November 2020

Waardenburg syndrome type IIE in a Japanese patient caused by a novel non-frame-shift duplication mutation in the SOX10 gene

scientific article published on 23 November 2017

List of works by Ken Okamura