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المؤلفون: Siro Bagnoli, Adele Acciarri, Benedetta Nacmias, Anna Poleggi, David R. Wekstein, Alessandra Bizzarro, Maria Puopolo, Carlo Masullo, Maria Giovanna Matera, Davide Seripa, Sandro Sorbi, A. Lauria, Maurizio Pocchiari, Elena Cellini, G. Dal Forno, Piero Antuono, Claudia Giannattasio
المصدر: European Journal of Neurology. 15:173-178
مصطلحات موضوعية: Genetics, Apolipoprotein E, business.industry, animal diseases, Apoe polymorphism, Disease, Virology, nervous system diseases, PRNP, Neurology, mental disorders, Medicine, Prnp gene, Neurology (clinical), Genetic risk factor, Prion protein, business, Gene
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المؤلفون: Adele Acciarri, Piero Antuono, David R. Wekstein, Carlo Masullo, Anna Poleggi, Maria Giovanna Matera, Alessandra Bizzarro, Maria Puopolo, Claudia Giannattasio, Davide Seripa, Gloria Dal Forno, Alessandra Lauria, Maurizio Pocchiari
المصدر: Dementia and Geriatric Cognitive Disorders. 25:354-358
مصطلحات موضوعية: Genetics, Apolipoprotein E, Cognitive Neuroscience, Disease, Biology, medicine.disease, Loss of heterozygosity, Psychiatry and Mental health, Degenerative disease, Genotype, medicine, Prnp gene, Geriatrics and Gerontology, Allele, Alzheimer's disease
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المؤلفون: Gabor G. Kovacs, Ellen Gelpi, Richard Knight, Herbert Budka, Sara Nocentini, Cornelia M. van Duijn, Anikó Gál, Mária Judit Molnár, Piero Parchi, Anna Poleggi, Uta Heinemann, Sabina Capellari, Claudia Giannattasio, Matthew Bishop, Eva Mitrova, Thomas Ströbel, Pascual Sánchez-Juan, Agnes Bakos, Inga Zerr, Maaike Schuur, Girma Belay
المساهمون: Neurology, Epidemiology, G G Kovac, P Sanchez-Juan, T Strobel, M Schuur, A Poleggi, S Nocentini, C Giannattasio, G Belay, M Bishop, S Capellari, P Parchi, E Gelpi, A Gal, A Bako, M J. Molnar, U Heinemann, I Zerr, Richar S.G. Knight, Eva Mitrova, Cornelia van Duijn, Herbert Budka, Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H.
المصدر: Kovacs, G G, Sanchez-Juan, P, Ströbel, T, Schuur, M, Poleggi, A, Nocentini, S, Giannattasio, C, Belay, G, Bishop, M, Capellari, S, Parchi, P, Gelpi, E, Gal, A, Bakos, A, Molnar, M J, Heinemann, U, Zerr, I, Knight, R S G, Mitrova, E, Van Duijn, C & Budka, H 2010, ' Cathepsin D (C224T) polymorphism in sporadic and genetic creutzfeldt-jakob disease ', Alzheimer Disease and Associated Disorders, vol. 24, no. 1, pp. 104-107 . https://doi.org/10.1097/WAD.0b013e3181ad378c
Alzheimer Disease & Associated Disorders, 24(1), 104-107. Lippincott Williams & Wilkins
Alzheimer Disease and Associated Disorders, 24(1), 104-107. Lippincott Williams and Wilkinsمصطلحات موضوعية: Adult, Male, Apolipoprotein E, Genotype, PRION, Cathepsin D, Biology, Polymorphism, Single Nucleotide, Creutzfeldt-Jakob Syndrome, CATHEPSIN, Exon, Degenerative disease, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Allele, Gene, Aged, Genetics, Middle Aged, medicine.disease, nervous system diseases, CJD, Psychiatry and Mental health, Clinical Psychology, Female, CTSD, Geriatrics and Gerontology, Gerontology
وصف الملف: STAMPA; ELETTRONICO
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9215efde25b4bf48b31058c4ba15ac
https://research.vumc.nl/en/publications/c96cd3e1-8268-425d-9389-b07ed57e60af -
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المؤلفون: Claudia Giannattasio, Cornelia M. van Duijn, Anna Poleggi, Pascual Sánchez-Juan, Richard Knight, Matthew Bishop, Alejandro Arias-Vásquez, Alison Green
المصدر: BMC Medical Genetics, 8, pp. 77-1-77
Sánchez-Juan, P, Bishop, M T, Green, A, Giannattasio, C, Arias-Vasquez, A, Poleggi, A, Knight, R S G & van Duijn, C M 2007, ' No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease ', BMC Medical Genetics, vol. 8, pp. 77 . https://doi.org/10.1186/1471-2350-8-77
BMC Medical Genetics
BMC Medical Genetics, Vol 8, Iss 1, p 77 (2007)
BMC Medical Genetics, 8, 77-1-77مصطلحات موضوعية: Adult, lcsh:Internal medicine, Linkage disequilibrium, lcsh:QH426-470, animal diseases, tau Proteins, Biology, Polymorphism, Single Nucleotide, Creutzfeldt-Jakob Syndrome, Linkage Disequilibrium, PRNP, Cognitive neurosciences [UMCN 3.2], Polymorphism (computer science), mental disorders, Genetic variation, Perception and Action [DCN 1], Genetics, Humans, Genetic Predisposition to Disease, Genetics(clinical), lcsh:RC31-1245, Gene, Genetics (clinical), Aged, Aged, 80 and over, Haplotype, Genetic Variation, Middle Aged, Virology, nervous system diseases, lcsh:Genetics, Open reading frame, Haplotypes, Genetic defects of metabolism [UMCN 5.1], Case-Control Studies, Functional Neurogenomics [DCN 2], Research Article
وصف الملف: application/pdf
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