Neuroprotection by S-PBN in hyperglycemic ischemic brain injury in rats

por Molnar, Maria, Lennmyr, Fredrik
Publicado 2010

Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries

por Zelei, Tamás, Molnár, Mária J., Szegedi, Márta, Kaló, Zoltán
Publicado 2016

Answer to Gerber et al. “Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy”

por Gál, Anikó, Santos, Janine H, Molnár, Mária Judit, Hajnóczky, György
Publicado 2023

Real-Life Clinical Experience With Cariprazine: A Systematic Review of Case Studies

por Csehi, Réka, Dombi, Zsófia Borbála, Sebe, Barbara, Molnár, Mária Judit
Publicado 2022

Early-Onset Schizophrenia With Predominantly Negative Symptoms: A Case Study of a Drug-Naive Female Patient Treated With Cariprazine

por Molnar, Maria Judit, Jimoh, Idris János, Zeke, Helga, Palásti, Ágnes, Fedor, Marianna
Publicado 2020

Predictiting valproate toxicity in patients with mitochondrial disorders

por Remenyi, Viktoria, Kekesi, Anna, Pentelenyi, Klara, Gal, Aniko, Hársfalvi, Vivien, Molnar, Maria Judit
Publicado 2014

Dynamic interaction of genetic risk factors and cocaine abuse in the background of Parkinsonism – a case report

por Illés, Anett, Balicza, Péter, Molnár, Viktor, Bencsik, Renáta, Szilvási, István, Molnar, Maria Judit
Publicado 2019

Polymyositis and rhabdomyolysis caused by hepatocellular carcinoma - Case report and literature review

por Bárdos, Dávid, Molnár, Mária Judit, Dudás, Ibolyka, Tuza, Sebestyén, Szijártó, Attila, Hahn, Oszkár
Publicado 2021

Breast Cancer Survivorship Programme: Follow-Up, Rehabilitation, Psychosocial Oncology Care. 1st Central-Eastern European Professional Consensus Statement on Breast Cancer

por Kahán, Zsuzsanna, Szántó, István, Dudás, Rita, Kapitány, Zsuzsanna, Molnár, Mária, Koncz, Zsuzsa, Mailáth, Mónika
Publicado 2022

Case report: The spectrum of SMPD1 pathogenic variants in Hungary

por Molnar, Maria Judit, Szlepak, Tamas, Csürke, Ildikó, Loth, Szendile, Káposzta, Rita, Erdős, Melinda, Dezsőfi, Antal
Publicado 2023

Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations

por Beke, Artur, Piko, Henriett, Haltrich, Iren, Karcagi, Veronika, Rigo, Janos, Molnar, Maria Judit, Fekete, György
Publicado 2018

A new family with transportinopathy: increased clinical heterogeneity

por Angelini, Corrado, Marozzo, Roberta, Pinzan, Elena, Pegoraro, Valentina, Molnar, Maria Judit, Torella, Annalaura, Nigro, Vincenzo
Publicado 2019

Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment

por Molnar, Maria Judit, Molnar, Viktor, Fedor, Mariann, Csehi, Reka, Acsai, Karoly, Borsos, Beata, Grosz, Zoltan
Publicado 2022

The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer’s Disease

por Csaban, Dora, Pentelenyi, Klara, Toth-Bencsik, Renata, Illes, Anett, Grosz, Zoltan, Gezsi, Andras, Molnar, Maria Judit
Publicado 2021

How bioinformatics influences health informatics: usage of biomolecular sequences, expression profiles and automated microscopic image analyses for clinical needs and public health

por Kuznetsov, Vladimir, Lee, Hwee Kuan, Maurer-Stroh, Sebastian, Molnár, Maria Judit, Pongor, Sandor, Eisenhaber, Birgit, Eisenhaber, Frank
Publicado 2013

New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family

por Toth-Bencsik, Renata, Balicza, Peter, Varga, Edina Timea, Lengyel, Andras, Rudas, Gabor, Gal, Aniko, Molnar, Maria Judit
Publicado 2021

The improvement of motor symptoms in Huntington’s disease during cariprazine treatment

por Csehi, Reka, Molnar, Viktor, Fedor, Mariann, Zsumbera, Vivien, Palasti, Agnes, Acsai, Karoly, Grosz, Zoltan, Nemeth, Gyorgy, Molnar, Maria Judit
Publicado 2023

Psychiatric symptoms of patients with primary mitochondrial DNA disorders

por Inczedy-Farkas, Gabriella, Remenyi, Viktoria, Gal, Aniko, Varga, Zsofia, Balla, Petra, Udvardy-Meszaros, Agnes, Bereznai, Benjamin, Molnar, Maria Judit
Publicado 2012

How to approach a neurogenetics diagnosis in different European countries: The European Academy of Neurology Neurogenetics Panel survey

por Mancuso, Michelangelo, Houlden, Henry, Molnar, Maria Judit, Filla, Alessandro, Breza, Marianthi, Graessner, Holm, Bassetti, Claudio L. A., Boesch, Sylvia
Publicado 2022

NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

por Balicza, Péter, Grosz, Zoltán, Molnár, Viktor, Illés, Anett, Csabán, Dora, Gézsi, Andras, Dézsi, Lívia, Zádori, Dénes, Vécsei, László, Molnár, Mária Judit
Publicado 2018