Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication von FUCHS, J, NILSSON, C, GASSER, T, FARRER, M. J, KACHERGUS, J, MUNZ, M, LARSSON, E.-M, SCHÜLE, B, LANGSTON, J. W, MIDDLETON, F. A, ROSS, O. A, HULIHAN, M

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NOVEL p.Ile151Val MUTATION IN VCP IN A PATIENT OF AFRICAN AMERICAN DESCENT WITH SPORADIC ALS von DEJESUS-HERNANDEZ, M, DESARO, P, JOHNSTON, A, ROSS, O. A, WSZOLEK, Z. K, ERTEKIN-TANER, N, GRAFF-RADFORD, N. R, RADEMAKERS, R, BOYLAN, K

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MAPT H1 HAPLOTYPE IS A RISK FACTOR FOR ESSENTIAL TREMOR AND MULTIPLE SYSTEM ATROPHY von VILARINO-GÜELL, C, SOTO-ORTOLAZA, A. I, FARRER, M. J, ROSS, O. A, RAJPUT, A, MASH, D. C, PAPAPETROPOULOS, S, PAHWA, R, LYONS, K. E, UITTI, R. J, WSZOLEK, Z. K, DICKSON, D. W

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Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population von TOFT, M, PIELSTICKER, L, ROSS, O. A, AASLY, J. O, FARRER, M. J

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CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA von OBI, T, NISHIOKA, K, HATTORI, N, ROSS, O. A, TERADA, T, YAMAZAKI, K, SUGIURA, A, TAKANASHI, M, MIZOGUCHI, K, MORI, H, MIZUNO, Y

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Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke von Heckman, M. G., Soto-Ortolaza, A. I., Diehl, N. N., Rayaprolu, S., Brott, T. G., Wszolek, Z. K., Meschia, J. F., Ross, O. A.

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A family with parkinsonism, essential tremor, restless legs syndrome, and depression von PUSCHMANN, A, PFEIFFER, R. F, DICKSON, D. W, WSZOLEK, Z. K, STOESSL, A. J, KURIAKOSE, R, LASH, J. L, SEARCY, J. A, STRONGOSKY, A. J, VILARINO-GÜELL, C, FARRER, M. J, ROSS, O. A

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PINK1 (PARK6) associated Parkinson disease in Ireland von HEALY, D. G, ABOU-SLEIMAN, P. M, GIBSON, J. M, ROSS, O. A, JAIN, S, GANDHI, S, GOSAL, D, MUQIT, M. M. K, WOOD, N. W, LYNCH, T

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Characterization of DCTN1 genetic variability in neurodegeneration von VILARINO-GÜELL, C, WIDER, C, UITTI, R. J, GRAFF-RADFORD, N. R, BOEVE, B. F, JOSEPHS, K. A, MILLER, B, BOYLAN, K. B, GWINN, K, ADLER, C. H, AASLY, J. O, HENTATI, F, SOTO-ORTOLAZA, A. I, DESTEE, A, KRYGOWSKA-WAJS, A, CHARTIER-HARLIN, M.-C, ROSS, O. A, RADEMAKERS, R, FARRER, M. J, COBB, S. A, KACHERGUS, J. M, KEELING, B. H, DACHSEL, J. C, HULIHAN, M. M, DICKSON, D. W, WSZOLEK, Z. K

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AN INDEPENDENT REPLICATION OF PARK16 IN ASIAN SAMPLES von VILARINO-GÜELL, C, ROSS, O. A, BARCIKOWSKA, M, LEE, M.-C, HENTATI, F, UITTI, R. J, WSZOLEK, Z. K, FARRER, M. J, WU, R.-M, AASLY, J. O, WHITE, L. R, RAJPUT, A, RAJPUT, A. H, LYNCH, T, KRYGOWSKA-WAJS, A, JASINSKA-MYGA, B, OPALA, G

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Atypical parkinsonian syndromes: a general neurologist's perspective von Deutschländer, A. B., Ross, O. A., Dickson, D. W., Wszolek, Z. K.

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TDP‐43 pathology in multiple system atrophy: colocalization of TDP‐43 and α‐synuclein in glial cytoplasmic inclusions von Koga, S., Lin, W.‐L., Walton, R. L., Ross, O. A., Dickson, D. W.

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Lrrk2 R1441 substitution and progressive supranuclear palsy von Ross, O. A., Whittle, A. J., Cobb, S. A., Hulihan, M. M., Lincoln, S. J., Toft, M., Farrer, M. J., Dickson, D. W.

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Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17) due to microtubule‐associated protein tau (MAPT) p.P301L mutation, inc... von Tacik, P., Sanchez‐Contreras, M., DeTure, M., Murray, M. E., Rademakers, R., Ross, O. A., Wszolek, Z. K., Parisi, J. E., Knopman, D. S., Petersen, R. C., Dickson, D. W.

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LRRK2 mutations are a common cause of Parkinson's disease in Spain von Mata, I. F., Ross, O. A., Kachergus, J., Huerta, C., Ribacoba, R., Moris, G., Blazquez, M., Guisasola, L. M., Salvador, C., Martinez, C., Farrer, M., Alvarez, V.

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Parkinsonism, Lrrk2 G2019S, and tau neuropathology von Rajput, A, Dickson, D W, Robinson, C A, Ross, O A, Dächsel, J C, Lincoln, S J, Cobb, S A, Rajput, M L, Farrer, M J

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Partial loss of function of colony‐stimulating factor 1 receptor in a patient with white matter abnormalities von Konno, T., Miura, T., Harriott, A. M., Mezaki, N., Edwards, E. S., Rademakers, R., Ross, O. A., Meschia, J. F., Ikeuchi, T., Wszolek, Z. K.

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Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations von Kachergus, Jennifer, Mata, Ignacio F., Hulihan, Mary, Taylor, Julie P., Lincoln, Sarah, Aasly, Jan, Gibson, J. Mark, Ross, Owen A., Lynch, Timothy, Wiley, Joseph, Payami, Haydeh, Nutt, John, Maraganore, Demetrius M., Czyzewski, Krzysztof, Styczynska, Maria, Wszolek, Zbigniew K., Farrer, Matthew J., Toft, Mathias

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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease von HAUGARVOLL, K, RADEMAKERS, R, GUIDI, M, RIBOLDAZZI, G, BROWN, L, WALTER, U, BENECKE, R, BERG, D, GASSER, T, THEUNS, J, PALS, P, CRAS, P, KACHERGUS, J. M, DE DEYN, P. Paul, ENGELBORGHS, S, PICKUT, B, UITTI, R. J, FOROUD, T, NICHOLS, W. C, HAGENAH, J, KLEIN, C, SAMII, A, ZABETIAN, C. P, NUYTEMANS, K, BONIFATI, V, VAN BROECKHOVEN, C, FARRER, M. J, WSZOLEK, Z. K, ROSS, O. A, GIBSON, J. M, TAN, E.-K, GAIG, C, TOLOSA, E, GOLDWURM, S

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Low density lipoprotein receptor related protein 1 and 6 gene variants and ischaemic stroke risk von Harriott, A. M., Heckman, M. G., Rayaprolu, S., Soto-Ortolaza, A. I., Diehl, N. N., Kanekiyo, T., Liu, C.-C., Bu, G., Malik, R., Cole, J. W., Meschia, J. F., Ross, O. A.

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