Viktoria Remenyi
Tömő Str. 25-29
Budapest, BU 1083, Hungary
Budapest, BU 1083, Hungary
Last Updated: 09/26/2026
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Found 9 publications
Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion.
Journal: Behavioral and brain functions : BBF
Published: August 24, 2017
The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation.
Journal: Ideggyogyaszati szemle
Published: February 28, 2015
The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy.
Journal: Clinical neuropathology
Published: December 11, 2014
Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease.
Journal: Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis
Published: September 23, 2014
Mitochondrial DNA mutations and cognition: a case-series report.
Journal: Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists
Published: April 30, 2014
Retrospective assessment of the most common mitochondrial DNA mutations in a large Hungarian cohort of suspect mitochondrial cases.
Journal: Mitochondrial DNA
Published: January 21, 2014
A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome.
Journal: Ideggyogyaszati szemle
Published: May 23, 2012
The effect of the CYP 2C19*2 polymorphism on stroke care.
Journal: Acta physiologica Hungarica
Published: March 20, 2012
Psychiatric symptoms of patients with primary mitochondrial DNA disorders.
Journal: Behavioral and brain functions : BBF
Published: September 29, 2011
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Last Updated: 09/26/2026