Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Claudia Giannattasio"'
Autor:
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
Publikováno v:
European Journal of Neurology. 15:173-178
Codon 129 polymorphism of the prion protein gene represents a major genetic risk factor for Creutzfeldt-Jakob disease (CJD). Both CJD and Alzheimer's disease (AD) are brain amyloidoses and it would be possible that codon 129 polymorphism plays a role
Autor:
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
Publikováno v:
Dementia and Geriatric Cognitive Disorders. 25:354-358
We assessed the role of the APOE genotype and prion protein polymorphism at codon 129 in predicting the clinical duration of 92 neuropathologically confirmed sporadic Alzheimer’s disease patients. Analyses of survival showed that the absence of the
Autor:
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
Publikováno v:
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 Wilkins
Alzheimer Disease & Associated Disorders, 24(1), 104-107. Lippincott Williams & Wilkins
Alzheimer Disease and Associated Disorders, 24(1), 104-107. Lippincott Williams and Wilkins
Accumulation of cathepsin D immunoreactive lysosomes correlates with tissue pathology in sporadic Creutzfeldt-Jakob disease (CJD) brains. The C-to-T transition within exon 2 of the cathepsin D (CTSD) gene is associated with altered enzymatic activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9215efde25b4bf48b31058c4ba15ac
https://research.vumc.nl/en/publications/c96cd3e1-8268-425d-9389-b07ed57e60af
https://research.vumc.nl/en/publications/c96cd3e1-8268-425d-9389-b07ed57e60af
Autor:
Claudia Giannattasio, Cornelia M. van Duijn, Anna Poleggi, Pascual Sánchez-Juan, Richard Knight, Matthew Bishop, Alejandro Arias-Vásquez, Alison Green
Publikováno v:
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, 77-1-77
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, 77-1-77
Background A polymorphism at codon 129 of the prion protein gene (PRNP) is the only well-known genetic risk factor for Creutzfeldt-Jakob disease (CJD). However, there is increasing evidence that other loci outside the PRNP open reading frame might pl