Muhammet E. Dogan

Kayseri, Turkey

Last Updated: 09/26/2026

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Found 25 publications

From Pustules to Pruritus: A Novel IL36RN Frameshift Variant Reveals a Triple Biologic Paradox and a Th17-To-Th2 Phenotypic Transition.

From Pustules to Pruritus: A Novel IL36RN Frameshift Variant Reveals a Triple Biologic Paradox and a Th17-To-Th2 Phenotypic Transition.

Journal: The Journal of dermatology

Published: May 23, 2026

A novel FLNA p.Pro2469Ser variant is associated with impaired T and NK cell function and immune dysregulation.

A novel FLNA p.Pro2469Ser variant is associated with impaired T and NK cell function and immune dysregulation.

Journal: Immunologic research

Published: May 14, 2026

A novel ELF4 gene variant disrupts T and NK cell function in a patient with immune thrombocytopenia (ITP).

A novel ELF4 gene variant disrupts T and NK cell function in a patient with immune thrombocytopenia (ITP).

Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]

Published: December 08, 2025

The Experience of a Tertiary Reference Center in Central Anatolia with Children Carrying ZAP-70 Variants, Including Two Novel Variants.

The Experience of a Tertiary Reference Center in Central Anatolia with Children Carrying ZAP-70 Variants, Including Two Novel Variants.

Journal: Journal of clinical immunology

Published: July 27, 2025

Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders.

Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders.

Journal: Research and practice in thrombosis and haemostasis

Published: January 28, 2025

A novel loss of function mutation in the HAVCR2 gene in a patient diagnosed with Hodgkin's lymphoma.

A novel loss of function mutation in the HAVCR2 gene in a patient diagnosed with Hodgkin's lymphoma.

Journal: Immunologic research

Published: December 17, 2024

A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.

Journal: American journal of medical genetics. Part A

Published: August 27, 2024

The clinical presentation and genetic diagnosis of Tangier disease in the pediatric age group.

The clinical presentation and genetic diagnosis of Tangier disease in the pediatric age group.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 13, 2024

A Novel Variant in AKAP9 Gene, a Controversial Gene, in Long QT Syndrome.

A Novel Variant in AKAP9 Gene, a Controversial Gene, in Long QT Syndrome.

Journal: Molecular syndromology

Published: August 05, 2023

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Journal: British journal of haematology

Published: December 09, 2022

EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities.

EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: June 28, 2022

A novel MTX2 gene splice site variant resulting in exon skipping, causing the recently described mandibuloacral dysplasia progeroid syndrome.

A novel MTX2 gene splice site variant resulting in exon skipping, causing the recently described mandibuloacral dysplasia progeroid syndrome.

Journal: American journal of medical genetics. Part A

Published: June 22, 2022

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Last Updated: 09/26/2026