Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population-Reference-Cited by-同舟云学术

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Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population

Published:2013-04-26 Issue:8 Volume:38 Page:911-916
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Israeli S.¹²,Goldberg I.¹,Fuchs-Telem D.¹²,Bergman R.³,Indelman M.³,Bitterman-Deutsch O.⁴,Harel A.⁵,Mashiach Y.¹⁵,Sarig O.¹,Sprecher E.¹²⁵

Affiliation:

1. Department of Dermatology; Tel Aviv Sourasky Medical Center; Tel Aviv Israel

2. Department of Human Molecular Genetics and Biochemistry; Sackler Faculty of Medicine; Tel Aviv University; Ramat Aviv Israel

3. Department of Dermatology; Rambam Medical Centre; Haifa Israel

4. Dermatology Clinic; Nahariya Western Galilee Hospital; Nahariya Israel

5. Pediatric Dermatology Unit; Dana Children's Hospital; Tel Aviv Israel

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12148/fullpdf

Reference23 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. Incidence of moderate to severe ichthyosis in the United States;Milstone;Arch Dermatol,2012

3. Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain;Hernandez-Martin;J Am Acad Dermatol,2012

4. Annual direct and indirect health costs of the congenital ichthyoses;Styperek;Pediatr Dermatol,2010

5. Recommendations for introducing genetics services in developing countries;Alwan;Nat Rev Genet,2003

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1. Compound heterozygous ABCA12 variants identified in a Chinese patient with congenital ichthyosiform erythroderma: Advancing genotype–phenotype correlations and literature review;Molecular Genetics & Genomic Medicine;2024-05

2. Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations;Genes;2024-02-24

3. Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population;International Ophthalmology;2023-08-05

4. A novel mutation compounded with a known mutation in TGM1 associated with severe lamellar ichthyosis and intellectual disability;European Journal of Dermatology;2023-08

5. Ophthalmic Findings in Patients with Autosomal Recessive Lamellar Ichthyosis due to TGM1 Mutations in an Isolated Population;2023-04-05

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