(PDF) Increased Prevalence of Filaggrin Deficiency in 51

Increased Prevalence of Filaggrin Deficiency in 51 Patients With Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

Journal of Investigative Dermatology - United Kingdom

doi 10.1016/j.jid.2017.08.047

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Date

March 1, 2018

Authors

Alberto Sánchez-Guijo

Publisher

Elsevier BV

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Increased Prevalence of Filaggrin Deficiency in 51 Patients With Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

Journal of Investigative Dermatology - United Kingdom

doi 10.1016/j.jid.2017.08.047

Full Text

Abstract

Categories

Date

Authors

Publisher

Related search

Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders

375 Modelling and Understanding Pathomechanisms of X-Linked Recessive Ichthyosis in Vitro

Cloning of a cDNA for Steroid Sulfatase: Frequent Occurrence of Gene Deletions in Patients With Recessive X Chromosome-Linked Ichthyosis.

X Linked Recessive Thrombocytopenia.

X‐linked Ichthyosis: Molecular Findings in Four Pedigrees With Inconspicuous Clinical Manifestations

G389(P) a Case for Early Ammonia Testing in All Encephalopathic Patients: Female Patients With X-Linked Ornithine Transcarbamylase Deficiency

Genetic Study of a New X-Linked Recessive Immunodeficiency Syndrome.

A Coinheritance of X-Linked and Autosomal Dominant Forms of the Ichthyosis

Functional Study ofTGM1missense Mutations in Autosomal Recessive Congenital Ichthyosis