Linda Ozoemena

St Thomas' Hospital
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 19 publications

Enamel Phenotype in Junctional Epidermolysis Bullosa.

Enamel Phenotype in Junctional Epidermolysis Bullosa.

Journal: The Journal of investigative dermatology
Published: November 26, 2024

Genotype-Phenotype Correlation in Junctional Epidermolysis Bullosa: Signposts to Severity.

Genotype-Phenotype Correlation in Junctional Epidermolysis Bullosa: Signposts to Severity.

Journal: The Journal of investigative dermatology
Published: May 18, 2023

A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter.

A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter.

Journal: JAAD case reports
Published: April 24, 2023

The natural history of laryngo-onycho-cutaneous syndrome: A case series of six pediatric patients and literature review.

The natural history of laryngo-onycho-cutaneous syndrome: A case series of six pediatric patients and literature review.

Journal: Pediatric dermatology
Published: September 13, 2021

PLACK syndrome: the penny dropped.

PLACK syndrome: the penny dropped.

Journal: Clinical and experimental dermatology
Published: July 15, 2020

Phase I/II open-label trial of intravenous allogeneic mesenchymal stromal cell therapy in adults with recessive dystrophic epidermolysis bullosa.

Phase I/II open-label trial of intravenous allogeneic mesenchymal stromal cell therapy in adults with recessive dystrophic epidermolysis bullosa.

Journal: Journal of the American Academy of Dermatology
Published: July 02, 2019

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa.

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa.

Journal: JCI insight
Published: December 05, 2018

Severe phenotype of junctional epidermolysis bullosa generalised intermediate type caused by homozygous COL17A1:c.505C>T (p.Arg169*) mutation.

Severe phenotype of junctional epidermolysis bullosa generalised intermediate type caused by homozygous COL17A1:c.505C>T (p.Arg169*) mutation.

Journal: European journal of dermatology : EJD
Published: June 29, 2018

Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait.

Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait.

Journal: International journal of dermatology
Published: November 01, 2017

A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report.

A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report.

Journal: BMC dermatology
Published: September 19, 2017

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex.

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex.

Journal: The Journal of investigative dermatology
Published: December 02, 2016

The p.Glu477Lys Mutation in Keratin 5 Is Strongly Associated with Mortality in Generalized Severe Epidermolysis Bullosa Simplex.

The p.Glu477Lys Mutation in Keratin 5 Is Strongly Associated with Mortality in Generalized Severe Epidermolysis Bullosa Simplex.

Journal: The Journal of investigative dermatology
Published: October 26, 2015
Showing 1-12 of 19

Last Updated: 09/26/2026