Resultados da busca - Alcalay, Roy

Neuropathology of Genetic Synucleinopathies with Parkinsonism – review of the literature por Schneider, Susanne A, Alcalay, Roy N.

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Precision medicine in Parkinson’s disease: emerging treatments for genetic Parkinson’s disease por Schneider, Susanne A., Alcalay, Roy N.

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Patients’ opinions on genetic counseling on the increased risk of Parkinson disease among Gaucher disease carriers por Mulhern, Maureen, Bier, Louise, Alcalay, Roy, Balwani, Manisha

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Emerging Targeted Therapeutics for Genetic Subtypes of Parkinsonism por Schneider, Susanne A., Hizli, Baccara, Alcalay, Roy N.

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Age-specific Parkinson disease risk in GBA mutation carriers: information for genetic counseling por Rana, Huma Q., Balwani, Manisha, Bier, Louise, Alcalay, Roy N.

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Urinary LRRK2 phosphorylation predicts parkinsonian phenotypes in G2019S LRRK2 carriers por Fraser, Kyle B., Moehle, Mark S., Alcalay, Roy N., West, Andrew B.

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Lack of Association Between Cancer History and PARKIN Genotype: a Family Based Study in PARKIN/Parkinson’s Families por Alcalay, Roy N., Clark, Lorraine N., Marder, Karen S., Bradley, W. Edward C.

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The “Head Snap”: A Subtle Clinical Feature During the Finger–Nose–Finger Maneuver in Essential Tremor por Sternberg, Eliezer J., Alcalay, Roy N., Levy, Oren A., Louis, Elan D.

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Postural and Intention Tremors: A Detailed Clinical Study of Essential Tremor vs. Parkinson’s Disease por Sternberg, Eliezer J., Alcalay, Roy N., Levy, Oren A., Louis, Elan D.

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Pure hereditary spastic paraplegia due to a de-novo mutation in the NIPA1 gene por Arkadir, David, Noreau, Anne, Goldman, Jill S., Rouleau, Guy A., Alcalay, Roy N.

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Movement Disorders Rounds: A Case of Missing Pathology in a Patient with LRRK2 Parkinson’s Disease por Agin-Liebes, Julian, Cortes, Etty, Vonsattel, Jean-Paul, Marder, Karen, Alcalay, Roy N.

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Essential Tremor-Parkinson’s Disease: A Double Whammy por Louis, Elan D., Wise, Adina, Alcalay, Roy N, Rao, Ashwini K., Factor-Litvak, Pam

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Lack of evidence for genetic association of saposins A, B, C and D with Parkinson’s disease por Sosero, Yuri Ludwig, Bandres-Ciga, Sara, Hassin-Baer, Sharon, Alcalay, Roy N, Gan-Or, Ziv

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Subnormal GM1 in PBMCs: Promise for Early Diagnosis of Parkinson’s Disease? por Alselehdar, Samar K., Chakraborty, Monami, Chowdhury, Suman, Alcalay, Roy N., Surface, Matthew, Ledeen, Robert

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Prevalence and Features of Unreported Dystonia in a Family Study of “Pure” Essential Tremor por Louis, Elan D., Hernandez, Nora, Alcalay, Roy N., Tirri, Dennis J, Ottman, Ruth, Clark, Lorraine N.

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Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson Disease por Galper, Jasmin, Balwani, Manisha, Fahn, Stanley, Waters, Cheryl, Krohn, Lynne, Gan‐Or, Ziv, Dzamko, Nicolas, Alcalay, Roy N.

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Attitudes Toward Telehealth Services Among People Living With Parkinson's Disease: A Survey Study por Xu, Yaqian, Feeney, Megan P., Surface, Matthew, Novak, Dan, Troche, Michelle S., Beck, James C., Alcalay, Roy N.

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Corticobasal syndrome in a man with Gaucher disease type 1: Expansion of the understanding of the neurological spectrum por Potnis, Kunal C., Flueckinger, Lauren B., DeArmey, Stephanie M., Alcalay, Roy N., Cooney, Jeffrey W., Kishnani, Priya S.

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Urinary proteome profiling for stratifying patients with familial Parkinson’s disease por Virreira Winter, Sebastian, Karayel, Ozge, Strauss, Maximilian T, Padmanabhan, Shalini, Surface, Matthew, Merchant, Kalpana, Alcalay, Roy N, Mann, Matthias

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Lipidomics prediction of Parkinson’s disease severity: A machine-learning analysis por Avisar, Hila, Guardia-Laguarta, Cristina, Area-Gomez, Estela, Surface, Matthew, Chan, Amanda K., Alcalay, Roy N., Lerner, Boaz

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