Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jody Lavrich"'
Autor:
Satish K. Nemani, Xiangzhu Xiao, Ignazio Cali, Laura Cracco, Gianfranco Puoti, Massimiliano Nigro, Jody Lavrich, Anuradha Bharara Singh, Brian S. Appleby, Valerie L. Sim, Silvio Notari, Witold K. Surewicz, Pierluigi Gambetti
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
Abstract One of remarkable features of sporadic Creutzfeldt-Jakob disease (sCJD) is the great phenotypic variability. Understanding the molecular basis of this variability has important implications for the development of therapeutic approaches. It i
Externí odkaz:
https://doaj.org/article/c9ed097c798c49debd92f73c5be253e7
Autor:
Laura Cracco, Xiangzhu Xiao, Satish K. Nemani, Jody Lavrich, Ignazio Cali, Bernardino Ghetti, Silvio Notari, Witold K. Surewicz, Pierluigi Gambetti
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-9 (2019)
Abstract Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-re
Externí odkaz:
https://doaj.org/article/ea9329de289a415c88f3286c662ceb27
Autor:
Romolo Nonno, Silvio Notari, Michele Angelo Di Bari, Ignazio Cali, Laura Pirisinu, Claudia d’Agostino, Laura Cracco, Diane Kofskey, Ilaria Vanni, Jody Lavrich, Piero Parchi, Umberto Agrimi, Pierluigi Gambetti
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 1, Pp 73-81 (2019)
Variably protease-sensitive prionopathy (VPSPr), a recently described human sporadic prion disease, features a protease-resistant, disease-related prion protein (resPrPD) displaying 5 fragments reminiscent of Gerstmann-Sträussler-Scheinker disease.
Externí odkaz:
https://doaj.org/article/ad97e37aa0e14c208f6fcf1cda0903b4
Autor:
Fabio Moda, Claudio Soto, Fabrizio Tagliavini, Satish K. Nemani, Jody Lavrich, Diane Kofskey, Pierluigi Gambetti, Silvio Notari, Ignazio Cali, Brian S. Appleby
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Scientific Reports
Scientific Reports
The presence of abnormal, disease-related prion protein (PrPD) has recently been demonstrated by protein misfolding cyclic amplification (PMCA) in urine of patients affected with variant Creutzfeldt-Jakob disease (vCJD), a prion disease typically acq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60650f79f7ba6fefb68460538696a18c
http://link.springer.com/article/10.1038/s41598-019-41694-0
http://link.springer.com/article/10.1038/s41598-019-41694-0
Autor:
Ilaria Vanni, Silvio Notari, Laura Cracco, Pierluigi Gambetti, Piero Parchi, Diane Kofskey, Ignazio Cali, Claudia D'Agostino, Jody Lavrich, Umberto Agrimi, Romolo Nonno, Michele Angelo Di Bari, Laura Pirisinu
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 1, Pp 73-81 (2019)
Emerging Infectious Diseases
Emerging Infectious Diseases
Variably protease-sensitive prionopathy (VPSPr), a recently described human sporadic prion disease, features a protease-resistant, disease-related prion protein (resPrPD) displaying 5 fragments reminiscent of Gerstmann-Sträussler-Scheinker disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d18ddcf6cbf018b51b33ba4b8e6c6d42
https://wwwnc.cdc.gov/eid/article/25/1/18-0807_article
https://wwwnc.cdc.gov/eid/article/25/1/18-0807_article
Autor:
Massimiliano Nigro, Silvio Notari, Brian S. Appleby, Valerie L. Sim, Gianfranco Puoti, Pierluigi Gambetti, Satish K. Nemani, Jody Lavrich, Laura Cracco, Witold K. Surewicz, Ignazio Cali, Anuradha Bharara Singh, Xiangzhu Xiao
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
One of remarkable features of sporadic Creutzfeldt-Jakob disease (sCJD) is the great phenotypic variability. Understanding the molecular basis of this variability has important implications for the development of therapeutic approaches. It is well es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ac7948af08cbea47736a3c26f9c6342
https://doi.org/10.1186/s40478-020-00966-x
https://doi.org/10.1186/s40478-020-00966-x
Autor:
Satish K. Nemani, Silvio Notari, Laura Cracco, Jody Lavrich, Ignazio Cali, Pierluigi Gambetti, Xiangzhu Xiao, Bernardino Ghetti, Witold K. Surewicz
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-9 (2019)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-related pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fc1f650bc5141f3185e542637a3227
https://doi.org/10.1186/s40478-019-0734-2
https://doi.org/10.1186/s40478-019-0734-2