Hasil Pencarian - Zoltán Grosz

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  1. 1
    Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment

    Improving Mood and Cognitive Symptoms in Huntington's Disease With Cariprazine Treatment oleh Maria Judit Molnar, Viktor Molnar, Mariann Fedor, Reka Csehi, Karoly Acsai, Beata Borsos, Zoltan Grosz

    Diterbitkan 2022-02-01
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  2. 2
    The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer’s Disease

    The Role of the Rare Variants in the Genes Encoding the Alpha-Ketoglutarate Dehydrogenase in Alzheimer’s Disease oleh Dora Csaban, Klara Pentelenyi, Renata Toth-Bencsik, Anett Illes, Zoltan Grosz, Andras Gezsi, Maria Judit Molnar

    Diterbitkan 2021-04-01
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  3. 3
    The improvement of motor symptoms in Huntington’s disease during cariprazine treatment

    The improvement of motor symptoms in Huntington’s disease during cariprazine treatment oleh Reka Csehi, Viktor Molnar, Mariann Fedor, Vivien Zsumbera, Agnes Palasti, Karoly Acsai, Zoltan Grosz, Gyorgy Nemeth, Maria Judit Molnar

    Diterbitkan 2023-12-01
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  4. 4
    Broadening the phenotype of the TWNK gene associated Perrault syndrome

    Broadening the phenotype of the TWNK gene associated Perrault syndrome oleh Bálint Fekete, Klára Pentelényi, Gabor Rudas, Anikó Gál, Zoltán Grosz, Anett Illés, Jimoh Idris, Gabor Csukly, Andor Domonkos, Maria Judit Molnar

    Diterbitkan 2019-12-01
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  5. 5
    The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials

    The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improvin... oleh Anett Illés, Dóra Csabán, Zoltán Grosz, Péter Balicza, András Gézsi, Viktor Molnár, Renáta Bencsik, Anikó Gál, Péter Klivényi, Maria Judit Molnar

    Diterbitkan 2019-10-01
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  6. 6
    NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement

    NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement oleh Péter Balicza, Zoltán Grosz, Viktor Molnár, Anett Illés, Dora Csabán, Andras Gézsi, Lívia Dézsi, Dénes Zádori, László Vécsei, László Vécsei, Mária Judit Molnár

    Diterbitkan 2018-08-01
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  7. 7
    Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease

    Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease oleh Aniko Gal, Zoltán Grosz, Beata Borsos, Ildikó Szatmari, Agnes Sebők, Laszló Jávor, Veronika Harmath, Katalin Szakszon, Livia Dezsi, Eniko Balku, Zita Jobbagy, Agnes Herczegfalvi, Zsuzsanna Almássy, Levente Kerényi, Maria Judit Molnar

    Diterbitkan 2021-05-01
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