Yasutoshi Ito

Nagoya, Japan

Last Updated: 09/26/2026

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Found 14 publications

Localized epidermolysis bullosa simplex caused by a previously unreported substitution in the linker 12 domain of keratin 14.

Localized epidermolysis bullosa simplex caused by a previously unreported substitution in the linker 12 domain of keratin 14.

Journal: The Journal of dermatology
Published: January 17, 2024

Two patients with Hailey-Hailey disease with novel pathogenic ATP2C1 variants suggesting possible genotype/phenotype correlations.

Two patients with Hailey-Hailey disease with novel pathogenic ATP2C1 variants suggesting possible genotype/phenotype correlations.

Journal: The Journal of dermatology
Published: October 02, 2023

Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes.

Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes.

Journal: The Journal of dermatology
Published: July 12, 2023

KLK11 ichthyosis: large truncal hyperkeratotic pigmented plaques underscore a distinct autosomal dominant disorder of cornification.

KLK11 ichthyosis: large truncal hyperkeratotic pigmented plaques underscore a distinct autosomal dominant disorder of cornification.

Journal: The British journal of dermatology
Published: January 03, 2023

Ceramide Analysis in Combination With Genetic Testing May Provide a Precise Diagnosis for Self-Healing Collodion Babies.

Ceramide Analysis in Combination With Genetic Testing May Provide a Precise Diagnosis for Self-Healing Collodion Babies.

Journal: Journal of lipid research
Published: July 01, 2022

Ceramide profiling of stratum corneum in Sjögren-Larsson syndrome.

Ceramide profiling of stratum corneum in Sjögren-Larsson syndrome.

Journal: Journal of dermatological science
Published: June 14, 2022

Case of ichthyosis with confetti caused by KRT10 mutation, complicated with multiple malignant melanomas.

Case of ichthyosis with confetti caused by KRT10 mutation, complicated with multiple malignant melanomas.

Journal: The Journal of dermatology
Published: December 07, 2021

Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing.

Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing.

Journal: European journal of dermatology : EJD
Published: April 19, 2021

Two Cases of Porokeratosis with MVD Mutations, in Association with Bullous Pemphigoid.

Two Cases of Porokeratosis with MVD Mutations, in Association with Bullous Pemphigoid.

Journal: Acta dermato-venereologica
Published: February 08, 2021

Updated allele frequencies of SERPINB7 founder mutations in Asian patients with Nagashima-type palmoplantar keratosis/keratoderma.

Updated allele frequencies of SERPINB7 founder mutations in Asian patients with Nagashima-type palmoplantar keratosis/keratoderma.

Journal: Journal of dermatological science
Published: December 08, 2020

Cutaneous malignant melanoma in an elderly patient with intermediate junctional epidermolysis bullosa.

Cutaneous malignant melanoma in an elderly patient with intermediate junctional epidermolysis bullosa.

Journal: The Journal of dermatology
Published: November 24, 2020

Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome.

Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome.

Journal: Nagoya journal of medical science
Published: September 02, 2020
Showing 1-12 of 14

Last Updated: 09/26/2026