Search Results - "Alcalay, R.N."

Alpha galactosidase A activity in Parkinson's disease by Alcalay, R.N., Wolf, P., Levy, O.A., Kang, U.J., Waters, C., Fahn, S., Ford, B., Kuo, S.H., Vanegas, N., Shah, H., Liong, C., Narayan, S., Pauciulo, M.W., Nichols, W.C., Gan-Or, Z., Rouleau, G.A., Chung, W.K., Oliva, P., Keutzer, J., Marder, K., Zhang, X.K.

“…Glucocerebrosidase (GCase, deficient in Gaucher disease) enzymatic activity measured in dried blood spots of Parkinson's Disease (PD) cases is within healthy…”
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The relation between depression and parkin genotype: The CORE-PD study by Srivastava, A, Tang, M.-X, Mejia-Santana, H, Rosado, L, Louis, E.D, Caccappolo, E, Comella, C, Colcher, A, Siderowf, A, Jennings, D, Nance, M, Bressman, S, Scott, W.K, Tanner, C, Mickel, S, Andrews, H, Waters, C, Fahn, S, Cote, L, Frucht, S, Ford, B, Alcalay, R.N, Ross, B, Orbe Reilly, M, Rezak, M, Novak, K, Friedman, J.H, Pfeiffer, R.D, Marsh, L, Hiner, B, Merle, D, Ottman, R, Clark, L.N, Marder, K

“…Abstract Background Mutations in parkin are a known genetic risk factor for early onset Parkinson’s disease (EOPD) but their role in non-motor manifestations…”
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Age-specific prevalence of Parkinson’s disease and possible parkinsonian syndrome in Gaucher disease: Real-world evidence from the ICGG Gaucher Registry by Alcalay, R.N., Mistry, P., Di Fonzo, A., Batista, J.L., Bianculli, P., Carwile, J.L., Perichon, G., Balwani, M.

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Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study by ALCALAY, R. N, CACCAPPOLO, E, LOUIS, E, COMELLA, C, COLCHER, A, JENNINGS, D, NANCE, M, BRESSMAN, S, SCOTT, W. K, TANNER, C, MICKEL, S, ANDREWS, H, MEJIA-SANTANA, H, WATERS, C, FAHN, S, COTE, L, FRUCHT, S, FORD, B, REZAK, M, NOVAK, K, FRIEDMAN, J. H, PFEIFFER, R, MARSH, L, TANG, M.-X, HINER, B, SIDEROWF, A, PAYAMI, H, MOLHO, E, FACTOR, S, OTTMAN, R, CLARK, L. N, MARDER, K, ROSADO, L, ORBE REILLY, M, RUIZ, D, ROSS, B, VERBITSKY, M, KISSELEV, S

“…To assess the cognitive phenotype of glucocerebrosidase (GBA) mutation carriers with early-onset Parkinson disease (PD). We administered a neuropsychological…”
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Analysis of heterozygous PRKN variants and copy number variations in Parkinson's disease by Yu, E., Krohn, L., Rudakov, U., Mufti, K., Ruskey, J.A., Asayesh, F., Estiar, M.A., Spiegelman, D., Greenbaum, L., Dauvilliers, Y., Dupre, N., Rouleau, G.A., Hassin-Baer, S., Fon, E.A., Alcalay, R.N., Gan-Or, Z.

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NPC1 variants are not associated with Parkinson's disease by Senkevich, K., Amar Bencheikh, B. Ouled, Rudakou, U., Yu, E., Mufti, K., Ruskey, J.A., Asayesh, F., Laurent, S.B., Spiegelman, D., Fahn, S., Waters, C., Monchi, O., Dauvilliers, Y., Alcalay, R.N., Dupré, N., Greenbaum, L., Hassin-Baer, S., Espay, A.J., Rouleau, G.A., Fon, E.A., Gan-Or, Z.

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Olfaction in Parkin heterozygotes and compound heterozygotes: The CORE-PD study by ALCALAY, R. N, SIDEROWF, A, FAHN, S, COTE, L, FRUCHT, S, FORD, B, ORBE-REILLY, M, ROSS, B, VERBITSKY, M, KISSELEV, S, COMELLA, C, COLCHER, A, OTTMAN, R, JENNINGS, D, NANCE, M, BRESSMAN, S, SCOTT, W. K, TANNER, C, MICKEL, S, REZAK, M, NOVAK, K. E, FRIEDMAN, J. H, PFEIFFER, R, CACCAPPOLO, E, MARSH, L, HINER, B, CLARK, L. N, MARDER, K, MEJIA-SANTANA, H, TANG, M.-X, ROSADO, L, LOUIS, E, RUIZ, D, WATERS, C

“…While Parkinson disease (PD) is consistently associated with impaired olfaction, one study reported better olfaction among Parkin mutation carriers than…”
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