Genome-Wide, Non-Invasive Prenatal Testing for rare chromosomal abnormalities: A systematic review and meta-analysis of diagnostic test accuracy
Konya, Marton, Czimbalmos, Agnes, Loczi, Lotti, Koi, Tamas, Turan, Caner, Nagy, Rita, Acs, Nandor, Hegyi, Peter, Varbiro, Szabolcs, Gal, Aniko
Published in PloS one (05.11.2024)
Published in PloS one (05.11.2024)
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Erratum To: MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
Gal, Aniko, Balicza, Peter, Weaver, David, Naghdi, Shamim, Joseph, Suresh K, Várnai, Péter, Gyuris, Tibor, Horváth, Attila, Nagy, Laszlo, Seifert, Erin L, Molnar, Maria Judit, Hajnóczky, György
Published in EMBO molecular medicine (07.08.2023)
Published in EMBO molecular medicine (07.08.2023)
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New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family
Toth-Bencsik, Renata, Balicza, Peter, Varga, Edina Timea, Lengyel, Andras, Rudas, Gabor, Gal, Aniko, Molnar, Maria Judit
Published in Frontiers in genetics (08.06.2021)
Published in Frontiers in genetics (08.06.2021)
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Wernicke–Korsakoff syndrome associated with mtDNA disease
Jimoh, Idris Janos, Sebe, Barbara, Balicza, Peter, Fedor, Mariann, Pataky, Ilona, Rudas, Gabor, Gal, Aniko, Inczedy-Farkas, Gabriella, Nemeth, Gyorgy, Molnar, Maria Judit
Published in Therapeutic advances in neurological disorders (2020)
Published in Therapeutic advances in neurological disorders (2020)
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Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene
Illés, Anett, Balicza, Péter, Gál, Anikó, Pentelényi, Klára, Csabán, Dóra, Gézsi, András, Molnár, Viktor, Molnár, Mária Judit
Published in Orvosi hetilap (01.05.2020)
Published in Orvosi hetilap (01.05.2020)
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Etiological factors of sensorineural hearing loss in children after cochlear implantation
Kecskeméti, Nóra, Gáborján, Anita, Szőnyi, Magdolna, Küstel, Marianna, Baranyi, Ildikó, Molnár, Mária Judit, Tamás, László, Gál, Anikó, Szirmai, Ágnes
Published in Orvosi hetilap (01.05.2019)
Published in Orvosi hetilap (01.05.2019)
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Psychiatric symptoms of patients with primary mitochondrial DNA disorders
Inczedy-Farkas, Gabriella, Remenyi, Viktoria, Gal, Aniko, Varga, Zsofia, Balla, Petra, Udvardy-Meszaros, Agnes, Bereznai, Benjamin, Molnar, Maria Judit
Published in Behavioral and brain functions (13.02.2012)
Published in Behavioral and brain functions (13.02.2012)
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Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease
Gal, Aniko, Grosz, Zoltán, Borsos, Beata, Szatmari, Ildikó, Sebők, Agnes, Jávor, Laszló, Harmath, Veronika, Szakszon, Katalin, Dezsi, Livia, Balku, Eniko, Jobbagy, Zita, Herczegfalvi, Agnes, Almássy, Zsuzsanna, Kerényi, Levente, Molnar, Maria Judit
Published in Life (Basel, Switzerland) (31.05.2021)
Published in Life (Basel, Switzerland) (31.05.2021)
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Journal Article
MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein
Gal, Aniko, Balicza, Peter, Weaver, David, Naghdi, Shamim, Joseph, Suresh K, Várnai, Péter, Gyuris, Tibor, Horváth, Attila, Nagy, Laszlo, Seifert, Erin L, Molnar, Maria Judit, Hajnóczky, György
Published in EMBO molecular medicine (01.07.2017)
Published in EMBO molecular medicine (01.07.2017)
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Significance of whole exome sequencing in the diagnostics of rare neurological diseases - own experiences through a case presenting with ataxia
Balicza, Péter, Grosz, Zoltán, Bencsik, Renáta, Illés, Anett, Gál, Anikó, Gézsi, András, Molnár, Mária Judit
Published in Orvosi hetilap (01.07.2018)
Published in Orvosi hetilap (01.07.2018)
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Bcl-2 or bcl-XL gene therapy increases neural plasticity proteins nestin and c-fos expression in PC12 cells
Gal, Aniko, Pentelenyi, Klara, Remenyi, Viktoria, Wappler, Edina A., Safrany, Geza, Skopal, Judit, Nagy, Zoltan
Published in Neurochemistry international (01.10.2009)
Published in Neurochemistry international (01.10.2009)
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The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation
Reményi, Viktória, Inczédy-Farkas, Gabriella, Gál, Anikó, Bereznai, Benjamin, Pál, Zsuzsanna, Karcagi, Veronica, Mechler, Ferenc, Molnár, Mária Judit
Published in Ideggyógyászati szemle (30.11.2014)
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Published in Ideggyógyászati szemle (30.11.2014)
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A8344G mutation of the mitochondrial DNA with typical mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome
Vastagh, Ildikó, Gál, Anikó, Reményi, Viktória, Semjén, Judit, Lukács, Tímea, Valikovics, Attila, Molnár, Mária Judit
Published in Ideggyógyászati szemle (30.11.2011)
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Published in Ideggyógyászati szemle (30.11.2011)
Journal Article
Natural and Induced Mitochondrial Phosphate Carrier Loss: DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION
Seifert, Erin L, Gál, Aniko, Acoba, Michelle G, Li, Qipei, Anderson-Pullinger, Lauren, Golenár, Tunde, Moffat, Cynthia, Sondheimer, Neal, Claypool, Steven M, Hajnóczky, György
Published in The Journal of biological chemistry (09.12.2016)
Published in The Journal of biological chemistry (09.12.2016)
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Journal Article
Analysis of mtDNA A3243G mutation frequency in Hungary
Gal, Aniko, Komlosi, Katalin, Maasz, Anita, Pentelenyi, Klara, Remenyi, Viktoria, Ovary, Csaba, Valikovics, Attila, Dioszeghy, Peter, Bereczki, Daniel, Melegh, Bela, Molnár, Maria Judit
Published in Central European journal of medicine (01.06.2010)
Published in Central European journal of medicine (01.06.2010)
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Two transgenic mouse models for β-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations
Kacso, Gergely, Ravasz, Dora, Doczi, Judit, Németh, Beáta, Madgar, Ory, Saada, Ann, Ilin, Polina, Miller, Chaya, Ostergaard, Elsebet, Iordanov, Iordan, Adams, Daniel, Vargedo, Zsuzsanna, Araki, Masatake, Araki, Kimi, Nakahara, Mai, Ito, Haruka, Gál, Aniko, Molnár, Mária J, Nagy, Zsolt, Patocs, Attila, Adam-Vizi, Vera, Chinopoulos, Christos
Published in Biochemical journal (15.10.2016)
Published in Biochemical journal (15.10.2016)
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MELAS syndrome mimicking somatoform disorder
Inczedy-Farkas, Gabriella, Remenyi, Viktoria, Meszaros, Agnes, Gal, Aniko, Blasko, Gyorgy, Bereznai, Benjamin, Molnar, Maria Judit
Published in Central European journal of medicine (01.12.2011)
Published in Central European journal of medicine (01.12.2011)
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