Lamellar Ichthyosis Due to ALOX12B Mutation-Reference-Cited by-同舟云学术

Lamellar Ichthyosis Due to ALOX12B Mutation

Published:2013-06 Issue:5 Volume:104 Page:443-444
ISSN:0001-7310
Container-title:Actas Dermo-Sifiliográficas
language:en
Short-container-title:Actas Dermo-Sifiliográficas

Author:

Osório F.,Leão M.,Azevedo F.,Magina S.

Publisher

Elsevier BV

Subject

Dermatology,Histology,Pathology and Forensic Medicine

Reference10 articles.

1. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009;Oji;J Am Acad Dermatol,2010

2. The genetics of ichthyosis: a primer for epidemiologists;Bale;J Invest Dermatol,1994

3. Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain;Hernandez-Martin;J Am Acad Dermatol,2011

4. Autosomal recessive congenital ichthyosis;Bale,1993

5. Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): evidence of founder effects;Rodriguez-Pazos;Br J Dermatol,2011

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1. Autosomal recessiveALOX12Bgene and consecutive collodion baby;BMJ Case Reports;2024-03

2. Case report of self-improving collodion ichthyosis in the newborn;Journal of International Medical Research;2023-10

3. Congenital ichthyosis: a multidisciplinary approach in a neonatal care unit;BMJ Case Reports;2023-02

4. Identification of the first congenital ichthyosis case caused by a homozygous deletion in the ALOX12B gene due to chromosome 17 mixed uniparental disomy;Frontiers in Genetics;2022-08-08

5. Successful Treatment of an Adult with Atopic Dermatitis and Lamellar Ichthyosis Using Dupilumab;Biologics: Targets and Therapy;2022-06