Sibel B. Karauzum

Antalya, Turkey

Last Updated: 09/26/2026

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Found 19 publications

MYH2 as a Potential Modifier of Clinical Severity in Facioscapulohumeral Muscular Dystrophy.

MYH2 as a Potential Modifier of Clinical Severity in Facioscapulohumeral Muscular Dystrophy.

Journal: Journal of molecular neuroscience : MN

Published: January 21, 2026

Human Umbilical Vein Endothelial Cells Express the DUX4 Protein: A Basis for Further Vascular Research.

Human Umbilical Vein Endothelial Cells Express the DUX4 Protein: A Basis for Further Vascular Research.

Journal: Turk patoloji dergisi

Published: September 18, 2025

Gut Microbiota and Short-Chain Fatty Acid Profiles in Facioscapulohumeral Dystrophy: Associations with Epigenetic Alterations.

Gut Microbiota and Short-Chain Fatty Acid Profiles in Facioscapulohumeral Dystrophy: Associations with Epigenetic Alterations.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: August 22, 2025

Identification of a presymptomatic and early disease signature for Amyotrophic Lateral Sclerosis (ALS): protocol of the premodiALS study.

Identification of a presymptomatic and early disease signature for Amyotrophic Lateral Sclerosis (ALS): protocol of the premodiALS study.

Journal: medRxiv : the preprint server for health sciences

Published: June 10, 2025

Identification of a presymptomatic and early disease signature for amyotrophic lateral sclerosis (ALS): protocol of the premodiALS study.

Identification of a presymptomatic and early disease signature for amyotrophic lateral sclerosis (ALS): protocol of the premodiALS study.

Journal: Neurological research and practice

Published: May 14, 2025

Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening.

Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening.

Journal: Journal of genetic counseling

Published: September 08, 2023

Does hand mirror morphology a useful diagnostic tool for the treatment decision of acute undifferentiated leukemia at admission?

Does hand mirror morphology a useful diagnostic tool for the treatment decision of acute undifferentiated leukemia at admission?

Journal: La Clinica terapeutica

Published: July 20, 2022

Analysis of DUX4 Expression in Bone Marrow and Re-Discussion of DUX4 Function in the Health and Disease.

Analysis of DUX4 Expression in Bone Marrow and Re-Discussion of DUX4 Function in the Health and Disease.

Journal: Turk patoloji dergisi

Published: December 02, 2021

Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals.

Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals.

Journal: Current neuropharmacology

Published: December 23, 2020

The clinical spectrum of a rare chromosomal abnormality: Isochromosome 18p.

The clinical spectrum of a rare chromosomal abnormality: Isochromosome 18p.

Journal: Genetic counseling (Geneva, Switzerland)

Published: January 01, 2016

Ultrasonographic and Cytogenetic Issues in Prenatal Diagnosis of Pallister Killian Syndrome.

Ultrasonographic and Cytogenetic Issues in Prenatal Diagnosis of Pallister Killian Syndrome.

Journal: Genetic counseling (Geneva, Switzerland)

Published: January 01, 2016

PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH.

PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH.

Journal: Genetic counseling (Geneva, Switzerland)

Published: December 03, 2015

Showing 1-12 of 19

Last Updated: 09/26/2026