GBA-associated Parkinson’s disease in Hungary: clinical features and genetic insights von Szlepák, Tamás, Kossev, Annabel P., Csabán, Dóra, Illés, Anett, Udvari, Szabolcs, Balicza, Péter, Borsos, Beáta, Takáts, Annamária, Klivényi, Péter, Molnár, Mária J.

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Two transgenic mouse models for β-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations von 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

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Exclusive neuronal expression of SUCLA2 in the human brain von Dobolyi, Arpád, Ostergaard, Elsebet, Bagó, Attila G., Dóczi, Tamás, Palkovits, Miklós, Gál, Aniko, Molnár, Mária J., Adam-Vizi, Vera, Chinopoulos, Christos

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Localization of SUCLA2 and SUCLG2 subunits of succinyl CoA ligase within the cerebral cortex suggests the absence of matrix substrate-level phosphorylation in glial cells of the hu... von Dobolyi, Arpád, Bagó, Attila G., Gál, Aniko, Molnár, Mária J., Palkovits, Miklós, Adam-Vizi, Vera, Chinopoulos, Christos

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Alterations in voltage-sensing of the mitochondrial permeability transition pore in ANT1-deficient cells von Doczi, Judit, Torocsik, Beata, Echaniz-Laguna, Andoni, Mousson de Camaret, Bénédicte, Starkov, Anatoly, Starkova, Natalia, Gál, Aniko, Molnár, Mária J, Kawamata, Hibiki, Manfredi, Giovanni, Adam-Vizi, Vera, Chinopoulos, Christos

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The prion protein in human neuromuscular diseases von Kovács, Gábor G, Kalev, Ognian, Gelpi, Ellen, Haberler, Christine, Wanschitz, Julia, Strohschneider, Michaela, Molnár, Mária J, László, Lajos, Budka, Herbert

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Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries von Zelei, Tamás, Molnár, Mária J, Szegedi, Márta, Kaló, Zoltán

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AI-based tools for the diagnosis and treatment of rare neurological disorders von Molnar, Maria J., Molnar, Viktor

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MAPT S305I mutation: implications for argyrophilic grain disease von 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

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Rare variants in PLXNA4 and Parkinson's disease von 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

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Awareness and care practices for rare neurologic diseases among senior neurologists: A global survey von Jang, Dae-Gyu, Federico, Antonio, Savelieff, Masha G., Grisold, Wolfgang, Mancuso, Michelangelo, Molnar, Maria J., Feldman, Eva L., Reynolds, Evan L.

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Transgenic mice with partial SUCLA2 deficiency exhibit increases in SUCLG2 expression, GTP-forming succinate-CoA ligase activity and blood carnitine esters von Kacso, Gergely, Ravasz, Dora, Doczi, Judit, Németh, Beáta, Madgar, Ory, Saada, Ann, Illin, Polina, Miller, Chaya, Ostergaard, Elsebet, Iordanov, Iordan, Adams, Daniel, Vargedo, Zsuzsanna, Araki, Masatake, Araki, Kimi, Ito, Haruka, Gál, Aniko, Molnár, Mária J., Adam-Vizi, Vera, Chinopoulos, Christos

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A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions von Tyynismaa, Henna, Ylikallio, Emil, Patel, Mehul, Molnar, Maria J., Haller, Ronald G., Suomalainen, Anu

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TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea von Kovacs, Gabor G., Murrell, Jill R., Horvath, Sandor, Haraszti, Laszlo, Majtenyi, Katalin, Molnar, Maria J., Budka, Herbert, Ghetti, Bernardino, Spina, Salvatore

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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 von 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

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Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease von 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

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Factors influencing the efficacy, longevity, and safety of electroporation-assisted plasmid-based gene transfer into mouse muscles von Molnar, Maria J, Gilbert, Rénald, Lu, Yifan, Liu, An-Bang, Guo, Athena, Larochelle, Nancy, Orlopp, Kristian, Lochmuller, Hanns, Petrof, Basil J, Nalbantoglu, Josephine, Karpati, George

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Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease von Schulte, Eva C., Mollenhauer, Brit, Zimprich, Alexander, Bereznai, Benjamin, Lichtner, Peter, Haubenberger, Dietrich, Pirker, Walter, Brücke, Thomas, Molnar, Maria J., Peters, Annette, Gieger, Christian, Trenkwalder, Claudia, Winkelmann, Juliane

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Establishing a Neurological-Psychiatric Biobank: Banking, informatics, ethics von Molnar, Maria J., Bencsik, Peter

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Cathepsin D (C224T) Polymorphism in Sporadic and Genetic Creutzfeldt-Jakob Disease von KOVACS, Gabor G, SANCHEZ-JUAN, Pascual, PARCHI, Piero, GELPI, Ellen, GAL, Aniko, BAKOS, Agnes, MOLNAR, Maria J, HEINEMANN, Uta, ZERR, Inga, KNIGHT, Richard S. G, MITROVA, Eva, VAN DUIJN, Cornelia, STRÖBEL, Thomas, BUDKA, Herbert, SCHUUR, Maaike, POLEGGI, Anna, NOCENTINI, Sara, GIANNATTASIO, Claudia, BELAY, Girma, BISHOP, Matthew, CAPELLARI, Sabina

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