Works matching AU Greenbaum, Lior

Results: 58
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    Adult-onset Alexander disease among patients of Jewish Syrian descent.

    Published in:
    Neurogenetics, 2023, v. 24, n. 4, p. 303, doi. 10.1007/s10048-023-00732-w
    By:
    • Anis, Saar;
    • Fay-Karmon, Tsvia;
    • Lassman, Simon;
    • Shbat, Fadi;
    • Lesman-Segev, Orit;
    • Mor, Nofar;
    • Barel, Ortal;
    • Dominissini, Dan;
    • Chorin, Odelia;
    • Pras, Elon;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon
    Publication type:
    Article
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    Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features.

    Published in:
    Annals of Clinical & Translational Neurology, 2023, v. 10, n. 4, p. 553, doi. 10.1002/acn3.51741
    By:
    • Dori, Amir;
    • Arad, Michael;
    • Wasserstrum, Yishay;
    • Pollak, Arthur;
    • Nikitin, Vera;
    • Ben‐David, Merav;
    • Shamash, Jana;
    • Nahum, Ayelet Hashachar;
    • Shavit‐Stein, Efrat;
    • Domachevsky, Liran;
    • Kuperstein, Rafael;
    • Dominissini, Dan;
    • Shelestovich, Natalia;
    • Sadeh, Menachem;
    • Pras, Elon;
    • Greenbaum, Lior
    Publication type:
    Article
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    The impact of early versus late levodopa administration.

    Published in:
    Journal of Neural Transmission, 2017, v. 124, n. 4, p. 471, doi. 10.1007/s00702-016-1669-4
    By:
    • Yahalom, Gilad;
    • Cohen, Oren;
    • Warmann-Alaluf, Naama;
    • Shabat, Chen;
    • Strauss, Hanna;
    • Elincx-Benizri, Sandra;
    • Israeli-Korn, Simon;
    • Stein, Esther;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon
    Publication type:
    Article
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    LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domain.

    Published in:
    NPJ Parkinson's Disease, 2025, v. 11, n. 1, p. 1, doi. 10.1038/s41531-025-00934-z
    By:
    • Parlar, Sitki Cem;
    • Senkevich, Konstantin;
    • Yu, Eric;
    • Ruskey, Jennifer A.;
    • Ahmad, Jamil;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Waters, Cheryl;
    • Monchi, Oury;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon;
    • Miliukhina, Irina;
    • Timofeeva, Alla;
    • Emelyanov, Anton;
    • Pchelina, Sofya;
    • Alcalay, Roy N.;
    • Fon, Edward A.;
    • Trempe, Jean-François
    Publication type:
    Article
    12

    Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?

    Published in:
    NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00809-9
    By:
    • Senkevich, Konstantin;
    • Parlar, Sitki Cem;
    • Chantereault, Cloe;
    • Yu, Eric;
    • Ahmad, Jamil;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Waters, Cheryl;
    • Monchi, Oury;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Miliukhina, Irina;
    • Timofeeva, Alla;
    • Emelyanov, Anton;
    • Pchelina, Sofya;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon;
    • Alcalay, Roy N.;
    • Gan-Or, Ziv
    Publication type:
    Article
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    GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 5, p. 1859, doi. 10.1093/brain/awac413
    By:
    • Senkevich, Konstantin;
    • Zorca, Cornelia E;
    • Dworkind, Aliza;
    • Rudakou, Uladzislau;
    • Somerville, Emma;
    • Yu, Eric;
    • Ermolaev, Alexey;
    • Nikanorova, Daria;
    • Ahmad, Jamil;
    • Ruskey, Jennifer A;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Fahn, Stanley;
    • Waters, Cheryl;
    • Monchi, Oury;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon;
    • Grenn, Francis P
    Publication type:
    Article
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    Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

    Published in:
    Brain: A Journal of Neurology, 2020, v. 143, n. 1, p. 234, doi. 10.1093/brain/awz350
    By:
    • Blauwendraat, Cornelis;
    • Reed, Xylena;
    • Krohn, Lynne;
    • Heilbron, Karl;
    • Bandres-Ciga, Sara;
    • Tan, Manuela;
    • Gibbs, J Raphael;
    • Hernandez, Dena G;
    • Kumaran, Ravindran;
    • Langston, Rebekah;
    • Bonet‐Ponce, Luis;
    • Alcalay, Roy N;
    • Hassin-Baer, Sharon;
    • Greenbaum, Lior;
    • Iwaki, Hirotaka;
    • Leonard, Hampton L;
    • Grenn, Francis P;
    • Ruskey, Jennifer A;
    • Sabir, Marya;
    • Ahmed, Sarah
    Publication type:
    Article
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    Vici syndrome in Israel: Clinical and molecular insights.

    Published in:
    Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.991721
    By:
    • Chorin, Odelia;
    • Hirsch, Yoel;
    • Rock, Rachel;
    • Sheelo, Liat Salzer;
    • Goldberg, Yael;
    • Mandel, Hanna;
    • Hershkovitz, Tova;
    • Fleischer, Nicole;
    • Greenbaum, Lior;
    • Katz, Uriel;
    • Barel, Ortal;
    • Hamed, Nasrin;
    • Ben-Zeev, Bruria;
    • Greenberger, Shoshana;
    • Samra, Nadra Nasser;
    • Zimmer, Michal Stern;
    • Raas-Rothschild, Annick;
    • Pode-Shakked, Ben
    Publication type:
    Article
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    Association of Rare Variants in ARSA with Parkinson's Disease.

    Published in:
    Movement Disorders, 2023, v. 38, n. 10, p. 1806, doi. 10.1002/mds.29521
    By:
    • Senkevich, Konstantin;
    • Beletskaia, Mariia;
    • Dworkind, Aliza;
    • Yu, Eric;
    • Ahmad, Jamil;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Fahn, Stanley;
    • Waters, Cheryl;
    • Monchi, Oury;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Greenbaum, Lior;
    • Hassin‐Baer, Sharon;
    • Nagornov, Ilya;
    • Tyurin, Alexandr;
    • Miliukhina, Irina;
    • Timofeeva, Alla;
    • Emelyanov, Anton
    Publication type:
    Article
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    Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease.

    Published in:
    Movement Disorders, 2021, v. 36, n. 1, p. 178, doi. 10.1002/mds.28299
    By:
    • Yu, Eric;
    • Rudakou, Uladzislau;
    • Krohn, Lynne;
    • Mufti, Kheireddin;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Estiar, Mehrdad A.;
    • Spiegelman, Dan;
    • Surface, Matthew;
    • Fahn, Stanley;
    • Waters, Cheryl H.;
    • Greenbaum, Lior;
    • Espay, Alberto J.;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Rouleau, Guy A.;
    • Hassin‐Baer, Sharon;
    • Fon, Edward A.;
    • Alcalay, Roy N.;
    • Gan‐Or, Ziv
    Publication type:
    Article
    43

    Investigation of the HSPG2 Gene in Tardive Dyskinesia – New Data and Meta-Analysis.

    Published in:
    Frontiers in Pharmacology, 2018, p. N.PAG, doi. 10.3389/fphar.2018.00974
    By:
    • Zai, Clement C.;
    • Lee, Frankie H.;
    • Tiwari, Arun K.;
    • Lu, Justin Y.;
    • Luca, Vincenzo de;
    • Maes, Miriam S.;
    • Herbert, Deanna;
    • Shahmirian, Anashe;
    • Cheema, Sheraz Y.;
    • Zai, Gwyneth C.;
    • Atukuri, Anupama;
    • Sherman, Michael;
    • Shaikh, Sajid A.;
    • Tampakeras, Maria;
    • Freeman, Natalie;
    • King, Nicole;
    • Müller, Daniel J.;
    • Greenbaum, Lior;
    • Lerer, Bernard;
    • Voineskos, Aristotle N.
    Publication type:
    Article
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