Edina T. Varga
Szeged, CS, Hungary
Last Updated: 09/26/2026
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Found 15 publications
New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family.
Journal: Frontiers in genetics
Published: November 13, 2020
Thyrotropin-Releasing-Hormone-Synthesizing Neurons of the Hypothalamic Paraventricular Nucleus Are Inhibited by Glycinergic Inputs.
Journal: Thyroid : official journal of the American Thyroid Association
Published: October 30, 2019
Localization of connexin 43 gap junctions and hemichannels in tanycytes of adult mice.
Journal: Brain research
Published: June 14, 2017
Identification of a Novel GLA Gene Mutation, p.Ile239Met, in Fabry Disease With a Predominant Cardiac Phenotype.
Journal: International heart journal
Published: May 13, 2017
Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients.
Journal: Neuromuscular disorders : NMD
Published: February 23, 2017
Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients.
Journal: Neuromuscular disorders : NMD
Published: March 21, 2016
Genetic background of the hereditary spastic paraplegia phenotypes in Hungary - An analysis of 58 probands.
Journal: Journal of the neurological sciences
Published: September 22, 2015
Amyloid-β1-42 Disrupts Synaptic Plasticity by Altering Glutamate Recycling at the Synapse.
Journal: Journal of Alzheimer's disease : JAD
Published: December 31, 2014
Retinal ganglion cell layer and visual function in patients with progressive external ophthalmoplegia caused by common mtDNA deletion
Journal: Ideggyogyaszati szemle
Published: December 19, 2014
Last Updated: 09/26/2026