المؤلفون: Fuchs, J, Nilsson, C, Kachergus, J, Munz, M, Larsson, E-M, Schüle, B, Langston, J W, Middleton, F A, Ross, O A, Hulihan, M, Gasser, T, Farrer, M J

المصدر: Fuchs , J , Nilsson , C , Kachergus , J , Munz , M , Larsson , E-M , Schüle , B , Langston , J W , Middleton , F A , Ross , O A , Hulihan , M , Gasser , T & Farrer , M J 2007 , ' Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication. ' , Neurology , vol. 68 , no. 12 , pp. 916-22 . https://doi.org/10.1212/01.wnl.0000254458.17630.c5Test

مصطلحات موضوعية: Adult, Aged, Americas, Autonomic Nervous System Diseases, Blood Proteins, Chromosomes, Human, Pair 4, DNA Mutational Analysis, Dementia, Female, Gene Dosage, Genealogy and Heraldry, Genetic Predisposition to Disease, Genetic Screening, Humans, Male, Microsatellite Repeats, Middle Aged, Mutation, Oligonucleotide Array Sequence Analysis, Parkinsonian Disorders, Pedigree, Phenotype, Sweden, Tomography, Emission-Computed, Single-Photon, alpha-Synuclein

الإتاحة: https://doi.org/10.1212/01.wnl.0000254458.17630.c5Test
https://pure.au.dk/portal/da/publications/phenotypic-variation-in-a-large-swedish-pedigree-due-to-snca-duplication-and-triplicationTest(f6acab00-eaba-11dc-9afb-000ea68e967b).html

المؤلفون: Tan E.K., Shen H., Tan L.C.S., Farrer M., Yew K., Chua E., Jamora R.D., Puvan K., Puong K.Y., Zhao Y., Pavanni R., Wong M.C., Yih Y., Skipper L., Liu J.-J.

المساهمون: PHARMACOLOGY, DUKE-NUS MEDICAL SCHOOL

المصدر: Scopus

مصطلحات موضوعية: LRRK2, Mutation, Parkinson's disease

العلاقة: Tan E.K., Shen H., Tan L.C.S., Farrer M., Yew K., Chua E., Jamora R.D., Puvan K., Puong K.Y., Zhao Y., Pavanni R., Wong M.C., Yih Y., Skipper L., Liu J.-J. (2005). The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neuroscience Letters 384 (3) : 327-329. ScholarBank@NUS Repository. https://doi.org/10.1016/j.neulet.2005.04.103Test; http://scholarbank.nus.edu.sg/handle/10635/150233Test

الإتاحة: https://doi.org/10.1016/j.neulet.2005.04.103Test
http://scholarbank.nus.edu.sg/handle/10635/150233Test

المؤلفون: Toft, M., Haugarvoll, K., Ross, O. A., Farrer, M. J., Aasly, J. O.

المصدر: Acta Neurologica Scandinavica: Supplementum; May2007 Supplement 187, Vol. 115, p72-75, 4p, 1 Chart, 1 Graph

مصطلحات موضوعية: PARKINSON'S disease, GENETIC mutation, GENETIC polymorphisms, POPULATION genetics

مصطلحات جغرافية: NORWAY

المؤلفون: 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.

المصدر: European Journal of Neurology; Apr2006, Vol. 13 Issue 4, p391-394, 4p, 2 Charts

مصطلحات موضوعية: PARKINSON'S disease, BRAIN diseases, GENETIC mutation, GENETICS, NEUROLOGY

مصطلحات جغرافية: ASTURIAS (Spain), SPAIN

المؤلفون: Rajput, A., Rajput, A. H., Rajput, M. L., Encarnacion, M., Bernales, C. Q., Ross, J. P., Farrer, M. J., Vilariño‐Güell, C.

المصدر: European Journal of Neurology; Feb2014, Vol. 21 Issue 2, p361-363, 3p

مصطلحات موضوعية: TREMOR, AMYOTROPHIC lateral sclerosis, MOTOR neuron diseases, MOVEMENT disorders, NEUROLOGIC manifestations of general diseases, NEUROMUSCULAR diseases