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Publications by Tatjana Tarinski

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

Journal of Investigative Dermatology

English

Related publications

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

Journal of the American Academy of Dermatology

Dermatology

2016

English

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

Journal of Investigative Dermatology

English

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

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

1987

English

X Linked Recessive Thrombocytopenia.

Journal of Medical Genetics

Genetics

1993

English

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

Journal of Clinical Laboratory Analysis

Medical Laboratory Technology

Clinical Biochemistry

English

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

Archives of Disease in Childhood

English

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

Journal of Clinical Investigation

Medicine

1992

English

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

Biomedical Journal of Scientific & Technical Research

2019

English

Functional Study ofTGM1missense Mutations in Autosomal Recessive Congenital Ichthyosis

Experimental Dermatology

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Tatjana Tarinski

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

Related publications

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