A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions
Tyynismaa, Henna, Ylikallio, Emil, Patel, Mehul, Molnar, Maria J., Haller, Ronald G., Suomalainen, Anu
Published in American journal of human genetics (14.08.2009)
Published in American journal of human genetics (14.08.2009)
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Breast Cancer Survivorship Programme: Follow-Up, Rehabilitation, Psychosocial Oncology Care. 1st Central-Eastern European Professional Consensus Statement on Breast Cancer
Kahán, Zsuzsanna, Szántó, István, Dudás, Rita, Kapitány, Zsuzsanna, Molnár, Mária, Koncz, Zsuzsa, Mailáth, Mónika
Published in Pathology oncology research (02.06.2022)
Published in Pathology oncology research (02.06.2022)
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The Panomics Approach in Neurodegenerative Disorders
Szatmari, Balazs, Balicza, Peter, Nemeth, Gyorgy, Molnar, Maria Judit
Published in Current medicinal chemistry (2019)
Published in Current medicinal chemistry (2019)
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TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
Kovacs, Gabor G., Murrell, Jill R., Horvath, Sandor, Haraszti, Laszlo, Majtenyi, Katalin, Molnar, Maria J., Budka, Herbert, Ghetti, Bernardino, Spina, Salvatore
Published in Movement disorders (15.09.2009)
Published in Movement disorders (15.09.2009)
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Mapping of European activities on the integration of sex and gender factors in neurology and neuroscience
Hentzen, Nina B., Ferretti, Maria Teresa, Santuccione Chadha, Antonella, Jaarsma, Joke, De Visser, Marianne, Moro, Elena, Aamodt, Anne Hege, Arabia, Gennarina, Aybeck, Selma, Carvalho, Vanessa, Goudier, Riadh, Grisold, Wolfgang, Lebedeva, Elena R., Matczack, Magda, Magyari, Melinda, Molnar, Maria Judit, Rakusa, Martin, Pajediene, Evelina, Tracy, Irene, Vonck, Kristl
Published in European journal of neurology (01.09.2022)
Published in European journal of neurology (01.09.2022)
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The transition of children with rare diseases from pediatric to adult care
Molnár, Mária Judit, Cs Sági, Judit, Szabó, Léna, Grosz, Zoltán
Published in Orvosi hetilap (18.12.2022)
Published in Orvosi hetilap (18.12.2022)
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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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Factors associated with the severity of COVID‐19 outcomes in people with neuromuscular diseases: Data from the International Neuromuscular COVID‐19 Registry
Pizzamiglio, Chiara, Pitceathly, Robert D. S., Lunn, Michael P., Brady, Stefen, De Marchi, Fabiola, Galan, Lucia, Heckmann, Jeannine M., Horga, Alejandro, Molnar, Maria J., Oliveira, Acary S. B., Pinto, Wladimir B. V. R., Primiano, Guido, Santos, Ernestina, Schoser, Benedikt, Servidei, Serenella, Sgobbi Souza, Paulo V., Venugopalan, Vishnu, Hanna, Michael G., Dimachkie, Mazen M., Machado, Pedro M., Lim, Albert, Elsaddig, Amar, Juanatey, Ana, Romeiro, Ana, Themistocleous, Andreas, Kiss‐Csenki, Annamaria, Guerrero Sola, Antonio, Patil, Anuja, Duggal, Ashish, Gabriel, Carolyn, Marshall, Charles, Record, Christopher, Allen, Claire, Bearden, David, Rathna Sabapathi, DeviPriya, R, Dileep, Vecchio, Domizia, Newman, Edward, Eshun, Edwin, Foo, Eng C., Bugiardini, Enrico, Burke, Georgina, Ramdharry, Gita, Gorman, Gràinne S., Kumar, Guru, Sivasathiaseelan, Harri, Braga Farias, Igor, Smuts, Izelle, Holt, James, Groothuis, Jan T., Pritchard, Jane, Wall, Jasmine, Gamez, Josep, Shakthi, K. J. S., Wannop, Kate, Brennan, Kathryn, Saavedra, Lillian, Clayton, Lisa, Househam, Liz, Skorupinska, Mariola, Laura, Matilde, Ciocca, Matteo, Zosmer, Maya, Dhamne, Megha, Mancuso, Michelangelo, Janssen, Mirian, Musumeci, Olimpia, Price, Olivia, Chinnery, Patrick F., Ambrose, Philip, Mehta, Puja R., Thomas, Rhys H., Horvath, Rita, McFarland, Robert, Nortley, Ross, Paterson, Ross W., Geraldes, Ruth, Keh, Ryan, Neshuku, Saara, Sasidharan, Sandhya, Menon R, Sarath, Raga, Sharika, Rinaldi, Simon, Yareeda, Sireesha, Desai, Soaham, Ramaratnam, Sridharan, Keddie, Stephen, Watson‐Fargie, Taylor, Evangelista, Teresinha, Sansone, Valeria, Nesbitt, Victoria, Macken, William L., Oktay, Yavuz
Published in European journal of neurology (01.02.2023)
Published in European journal of neurology (01.02.2023)
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Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease
Schulte, Eva C, Fukumori, Akio, Mollenhauer, Brit, Hor, Hyun, Arzberger, Thomas, Perneczky, Robert, Kurz, Alexander, Diehl-Schmid, Janine, Hüll, Michael, Lichtner, Peter, Eckstein, Gertrud, Zimprich, Alexander, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J, Lorenzo-Betancor, Oswaldo, Pastor, Pau, Peters, Annette, Gieger, Christian, Estivill, Xavier, Meitinger, Thomas, Kretzschmar, Hans A, Trenkwalder, Claudia, Haass, Christian, Winkelmann, Juliane
Published in European journal of human genetics : EJHG (01.10.2015)
Published in European journal of human genetics : EJHG (01.10.2015)
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Rare variants in PLXNA4 and Parkinson's disease
Schulte, Eva C, Stahl, Immanuel, Czamara, Darina, Ellwanger, Daniel C, Eck, Sebastian, Graf, Elisabeth, Mollenhauer, Brit, Zimprich, Alexander, Lichtner, Peter, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Bereznai, Benjamin, Molnar, Maria J, Peters, Annette, Gieger, Christian, Müller-Myhsok, Bertram, Trenkwalder, Claudia, Winkelmann, Juliane
Published in PloS one (11.11.2013)
Published in PloS one (11.11.2013)
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GDF-15 and mtDNA Deletions Are Useful Biomarkers of Mitochondrial Dysfunction in Insulin Resistance and PCOS
Varhegyi, Vera, Modos, Anna, Trager, Domonkos, Gerszi, Dora, Horvath, Eszter Maria, Sipos, Miklos, Acs, Nandor, Molnar, Maria Judit, Varbiro, Szabolcs, Gal, Aniko
Published in International journal of molecular sciences (10.10.2024)
Published in International journal of molecular sciences (10.10.2024)
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How to approach a neurogenetics diagnosis in different European countries: The European Academy of Neurology Neurogenetics Panel survey
Mancuso, Michelangelo, Houlden, Henry, Molnar, Maria Judit, Filla, Alessandro, Breza, Marianthi, Graessner, Holm, Bassetti, Claudio L. A., Boesch, Sylvia
Published in European journal of neurology (01.07.2022)
Published in European journal of neurology (01.07.2022)
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Head-to-head trial of pegunigalsidase alfa versus agalsidase beta in patients with Fabry disease and deteriorating renal function: results from the 2-year randomised phase III BALANCE study
Wallace, Eric L, Goker-Alpan, Ozlem, Wilcox, William R, Holida, Myrl, Bernat, John, Longo, Nicola, Linhart, Aleš, Hughes, Derralynn A, Hopkin, Robert J, Tøndel, Camilla, Langeveld, Mirjam, Giraldo, Pilar, Pisani, Antonio, Germain, Dominique Paul, Mehta, Ankit, Deegan, Patrick B, Molnar, Maria Judit, Ortiz, Damara, Jovanovic, Ana, Muriello, Michael, Barshop, Bruce A, Kimonis, Virginia, Vujkovac, Bojan, Nowak, Albina, Geberhiwot, Tarekegn, Kantola, Ilkka, Knoll, Jasmine, Waldek, Stephen, Nedd, Khan, Karaa, Amel, Brill-Almon, Einat, Alon, Sari, Chertkoff, Raul, Rocco, Rossana, Sakov, Anat, Warnock, David G
Published in Journal of medical genetics (01.06.2024)
Published in Journal of medical genetics (01.06.2024)
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The improvement of motor symptoms in Huntington’s disease during cariprazine treatment
Csehi, Reka, Molnar, Viktor, Fedor, Mariann, Zsumbera, Vivien, Palasti, Agnes, Acsai, Karoly, Grosz, Zoltan, Nemeth, Gyorgy, Molnar, Maria Judit
Published in Orphanet journal of rare diseases (01.12.2023)
Published in Orphanet journal of rare diseases (01.12.2023)
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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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MAPT S305I mutation: implications for argyrophilic grain disease
Kovacs, Gabor G., Pittman, Alan, Revesz, Tamas, Luk, Connie, Lees, Andrew, Kiss, Eva, Tariska, Peter, Laszlo, Lajos, Molnár, Kinga, Molnar, Maria J., Tolnay, Markus, de Silva, Rohan
Published in Acta neuropathologica (01.07.2008)
Published in Acta neuropathologica (01.07.2008)
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Sex steroid hormones and epilepsy: Effects of hormonal replacement therapy on seizure frequency of postmenopausal women with epilepsy—A systematic review
Carvalho, Vanessa, Colonna, Isabella, Curia, Giulia, Ferretti, Maria Teresa, Arabia, Gennarina, Molnar, Maria Judit, Lebedeva, Elena R., Moro, Elena, Visser, Marianne, Bui, Esther, Aybek, Selma, Hege Aamodt, Anne, Goudier, Riadh, Grisold, Wolfgang, Jaarsma, Joke, Matczack, Magda, Magyari, Melinda, Rakusa, Martin, Pajediene, Evelina, Tracey, Irene, Vonck, Kristl, Zedde, Marialuisa
Published in European journal of neurology (01.09.2023)
Published in European journal of neurology (01.09.2023)
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