Martin Gencik

Vienna, Austria

Last Updated: 09/26/2026

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Found 13 publications

Bimaxillary fixed implant-supported zirconium oxide prosthesis therapy of an adolescent patient with non-syndromic oligodontia and two WNT10 variants: a case report.

Bimaxillary fixed implant-supported zirconium oxide prosthesis therapy of an adolescent patient with non-syndromic oligodontia and two WNT10 variants: a case report.

Journal: Annals of medicine and surgery (2012)

Published: January 29, 2024

Gene Variants Determine Placental Transfer of Perfluoroalkyl Substances (PFAS), Mercury (Hg) and Lead (Pb), and Birth Outcome: Findings From the UmMuKi Bratislava-Vienna Study.

Gene Variants Determine Placental Transfer of Perfluoroalkyl Substances (PFAS), Mercury (Hg) and Lead (Pb), and Birth Outcome: Findings From the UmMuKi Bratislava-Vienna Study.

Journal: Frontiers in genetics

Published: February 06, 2021

Report of a Second Lebanese Family with Basel-Vanagaite-Smirin-Yosef Syndrome: Possible Founder Mutation.

Report of a Second Lebanese Family with Basel-Vanagaite-Smirin-Yosef Syndrome: Possible Founder Mutation.

Journal: Molecular syndromology

Published: May 11, 2019

The Lebanese Allele in the PET100 Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency.

The Lebanese Allele in the PET100 Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency.

Journal: Journal of pediatric genetics

Published: October 16, 2018

A novel nonsense autosomal dominant mutation in the GLRA1 gene causing hyperekplexia.

A novel nonsense autosomal dominant mutation in the GLRA1 gene causing hyperekplexia.

Journal: Journal of neural transmission (Vienna, Austria : 1996)

Published: June 15, 2018

Familial accumulation of sudden cardiac deaths and the LMNA variant c.868G>A (p.Glu290Lys).

Familial accumulation of sudden cardiac deaths and the LMNA variant c.868G>A (p.Glu290Lys).

Journal: International journal of cardiology

Published: April 02, 2016

The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA.

The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA.

Journal: Clinical genetics

Published: November 21, 2015

Hereditary Neuropathy with Liability to Pressure Palsies Masked by Previous Gunshots and Tuberculosis.

Hereditary Neuropathy with Liability to Pressure Palsies Masked by Previous Gunshots and Tuberculosis.

Journal: Case reports in genetics

Published: July 25, 2015

Myotonic dystrophy 2 manifesting with non-alcoholic and non-hepatitic liver cirrhosis.

Myotonic dystrophy 2 manifesting with non-alcoholic and non-hepatitic liver cirrhosis.

Journal: Acta clinica Belgica

Published: July 04, 2015

Syncope and hyperCKemia as minimal manifestations of short CTG repeat expansions in myotonic dystrophy type 1.

Syncope and hyperCKemia as minimal manifestations of short CTG repeat expansions in myotonic dystrophy type 1.

Journal: Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology

Published: September 01, 2014

Recurrent takotsubo syndrome in a patient with myotonic dystrophy 1.

Recurrent takotsubo syndrome in a patient with myotonic dystrophy 1.

Journal: Acute cardiac care

Published: August 08, 2014

Noncompaction predisposing for recurrent Takotsubo syndrome in myotonic dystrophy 1.

Noncompaction predisposing for recurrent Takotsubo syndrome in myotonic dystrophy 1.

Journal: International journal of cardiology

Published: May 14, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026