Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy von Kapás, I., Katkó, M., Harangi, M., Paragh, G., Balogh, I., Kóczi, Z., Regelsberger, G., Molnár, M. J., Kovacs, G. G.

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The typical MERRF (A8344G) mutation of the mitochondrial DNA associated with depressive mood disorders von Molnar, M. J., Perenyi, J., Siska, E., Nemeth, G., Nagy, Z.

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Peripheral nerve and skeletal muscle involvement in CADASIL von Schröder, J M, Züchner, S, Dichgans, M, Nagy, Z, Molnar, M J

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Marked phenotypic variation in a family with a new myelin protein zero mutation von Szabo, A., Züchner, S., Siska, E., Mechler, F., Molnar, M.J.

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Cerebral blood flow and glucose metabolism in mitochondrial disorders von MOLNAR, M. J, VALIKOVICS, A, MOLNAR, S, TRON, L, DIOSZEGHY, P, MECHLER, F, GULYAS, B

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Molecular therapy for genetic muscle diseases : status 1999 von KARPATI, G, PARI, G, MOLNAR, M. J

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Challenging previous conceptions of vegetarianism and eating disorders von Fisak, Jr, B, Peterson, R D, Tantleff-Dunn, S, Molnar, J M

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A7.4 Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases von Pál, Z, Antal, P, Srivastava, SK, Gál, J, André, S, Gordeeva, E, Nagy, G, Kaltner, H, Bovin, NV, Molnár, MJ, Falus, A, Gabius, HJ, Buzás, EI

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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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Lighting for greenhouse vegetable production--an overview von Ehret, D.L, Jolliffe, P.A, Molnar, J.M

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Complement fragments and the pathogenesis of polymyositis von Basta, M., Molnar, M.J., Dupuy, P.

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A7.4Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases von Pal, Z, Antal, P, Srivastava, S K, Gal, J, Andre, S, Gordeeva, E, Nagy, G, Kaltner, H, Bovin, N V, Molnar, MJ, Falus, A, Gabius, HJ, Buzas, E I

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Beneficial effect of epidural anesthesia on oxygen consumption in a parturient with adult respiratory distress syndrome von Ackerman, 3rd, W E, Molnar, J M, Juneja, M M

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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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Cerebrotendinous xanthomatosis with the c.379 C > T (p. R 127 W ) mutation in the CYP27A1 gene associated with premature age‐associated limbic tauopathy von Kapás, I., Katkó, M., Harangi, M., Paragh, G., Balogh, I., Kóczi, Z., Regelsberger, G., Molnár, M. J., Kovacs, G. G.

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Multi-disciplinary Insights from the First European Forum on Visceral Myopathy 2022 Meeting von Viti, F, De Giorgio, R, Ceccherini, I, Ahluwalia, A, Alves, MM, Baldo, C, Baldussi, G, Bonora, E, Borrelli, O, Dall’Oglio, L, De Coppi, P, De Filippo, C, de Santa Barbara, P, Diamanti, A, Di Lorenzo, C, Di Maulo, R, Galeone, A, Gandullia, P, Hashmi, SK, Lacaille, F, Lancon, L, Leone, S, Mahé, MM, Molnar, MJ, Palmitelli, A, Perin, S, Prato, AP, Thapar, N, Vassalli, M, Heuckeroth, RO

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RIEGER ELATIOR BEGONIA CV. NORTHERN SUNSET von MOLNAR, J. M.

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ALSTROEMERIA ALSAAN von LIN, W. C., MOLNAR, J. M.

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RIEGER ELATIOR BEGONIA SAANRED von LIN, W. C., MOLNAR, J. M.

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The European Reference Network for Rare Neurological Diseases von Reinhard, C, Bachoud-Levi, A-C, Baeumer, T, Bertini, E, Brunelle, A, Buizer, AI, Federico, A, Gasser, T, Groeschel, S, Hermanns, S, Klockgether, T, Kraegeloh-Mann, I, Landwehrmeyer, GB, Leber, I, Macaya, A, Mariotti, C, Meissner, WG, Molnar, MJ, Nonnekes, J, Ortigoza Escobar, JD, Perez Duenas, B, Renna Linton, L, Schoels, L, Schuele, R, Tijssen, MAJ, Vandenberghe, R, Volkmer, A, Wolf, NI, Graessner, H

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