Lukas Varga

Head And Neck Surgery, Antolská 11
Bratislava, BL 85107, Slovakia

Last Updated: 09/26/2026

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Found 23 publications

European consensus statements on pediatric cochlear implantation.

European consensus statements on pediatric cochlear implantation.

Journal: International journal of pediatric otorhinolaryngology

Published: May 21, 2026

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic Patients.

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic Patients.

Journal: Ear and hearing

Published: February 10, 2026

Ageing, Sex Differences, and REDs Risk in Endurance Runners: An Integrated Cross-Sectional Study Protocol.

Ageing, Sex Differences, and REDs Risk in Endurance Runners: An Integrated Cross-Sectional Study Protocol.

Journal: Sports (Basel, Switzerland)

Published: January 09, 2026

Genetic heterogeneity in patients with enlarged vestibular aqueduct and Pendred syndrome.

Genetic heterogeneity in patients with enlarged vestibular aqueduct and Pendred syndrome.

Journal: Molecular medicine (Cambridge, Mass.)

Published: March 26, 2025

MEDAG functions as an A-kinase-anchoring protein in adipocytes.

MEDAG functions as an A-kinase-anchoring protein in adipocytes.

Journal: Molecular cell

Published: January 29, 2025

Slovak Translation and Cross-Cultural Validation of the Eating Assessment Tool (EAT10®).

Slovak Translation and Cross-Cultural Validation of the Eating Assessment Tool (EAT10®).

Journal: Journal of clinical medicine

Published: July 14, 2022

Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss.

Comprehensive molecular-genetic analysis of mid-frequency sensorineural hearing loss.

Journal: Scientific reports

Published: August 27, 2021

The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes-A Comprehensive Study of the GJB2/DFNB1 Region.

The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes-A Comprehensive Study of the GJB2/DFNB1 Region.

Journal: Genes

Published: March 23, 2021

Novel variants in EDNRB gene in Waardenburg syndrome type II and SOX10 gene in PCWH syndrome.

Novel variants in EDNRB gene in Waardenburg syndrome type II and SOX10 gene in PCWH syndrome.

Journal: International journal of pediatric otorhinolaryngology

Published: September 20, 2020

Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant.

Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant.

Journal: Orphanet journal of rare diseases

Published: June 15, 2020

Cold Exposure Distinctively Modulates Parathyroid and Thyroid Hormones in Cold-Acclimatized and Non-Acclimatized Humans.

Cold Exposure Distinctively Modulates Parathyroid and Thyroid Hormones in Cold-Acclimatized and Non-Acclimatized Humans.

Journal: Endocrinology

Published: March 20, 2020

Hereditary bilateral sudden sensorineural hearing loss.

Hereditary bilateral sudden sensorineural hearing loss.

Journal: Bratislavske lekarske listy

Published: September 03, 2019

Showing 1-12 of 23

Last Updated: 09/26/2026