Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Anna Ladogana"'
Autor:
Holger Hummerich, Helen Speedy, Tracy Campbell, Lee Darwent, Elizabeth Hill, Steven Collins, Christiane Stehmann, Gabor G Kovacs, Michael D Geschwind, Karl Frontzek, Herbert Budka, Ellen Gelpi, Adriano Aguzzi, Sven J van der Lee, Cornelia M van Duijn, Pawel P Liberski, Miguel Calero, Pascual Sanchez-Juan, Elodie Bouaziz-Amar, Jean-Louis Laplanche, Stéphane Haïk, Jean-Phillipe Brandel, Angela Mammana, Sabina Capellari, Anna Poleggi, Anna Ladogana, Maurizio Pocchiari, Saima Zafar, Stephanie Booth, Gerard H Jansen, Aušrinė Areškevičiūtė, Eva Løbner Lund, Katie Glisic, Piero Parchi, Peter Hermann, Inga Zerr, Brian S Appleby, Jiri Safar, Pierluigi Gambetti, John Collinge, Simon Mead
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0304528 (2024)
Human prion diseases are rare, transmissible and often rapidly progressive dementias. The most common type, sporadic Creutzfeldt-Jakob disease (sCJD), is highly variable in clinical duration and age at onset. Genetic determinants of late onset or slo
Externí odkaz:
https://doaj.org/article/a8105e366d44473aa02be9676f81d759
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
Prion diseases are rapidly progressive, invariably fatal, transmissible neurodegenerative disorders associated with the accumulation of the amyloidogenic form of the prion protein in the central nervous system (CNS). In humans, prion diseases are hig
Externí odkaz:
https://doaj.org/article/607b833ff69b49488b34ca60c791d22a
Autor:
Christina D. Orrú, Bradley R. Groveman, Aaron Foutz, Matilde Bongianni, Franco Cardone, Neil McKenzie, Audrey Culeux, Anna Poleggi, Katarina Grznarova, Daniela Perra, Michele Fiorini, Xiaoqin Liu, Anna Ladogana, Marco Sbriccoli, Andrew G. Hughson, Stéphane Haïk, Alison J. Green, Michael D. Geschwind, Maurizio Pocchiari, Jiri G. Safar, Gianluigi Zanusso, Byron Caughey
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 11, Pp 2262-2271 (2020)
Abstract Objective Real‐time quaking‐induced conversion (RT‐QuIC) assays detect prion‐seeding activity in a variety of human biospecimens, including cerebrospinal fluid and olfactory mucosa swabs. The assay has shown high diagnostic accuracy
Externí odkaz:
https://doaj.org/article/bb5874f625804d7ba24ed64e6f1053e6
Autor:
Matilde Bongianni, Anna Ladogana, Stefano Capaldi, Sigrid Klotz, Simone Baiardi, Annachiara Cagnin, Daniela Perra, Michele Fiorini, Anna Poleggi, Giuseppe Legname, Tatiana Cattaruzza, Francesco Janes, Massimo Tabaton, Bernardino Ghetti, Salvatore Monaco, Gabor G. Kovacs, Piero Parchi, Maurizio Pocchiari, Gianluigi Zanusso
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 10, Pp 2120-2126 (2019)
Abstract We applied RT‐QuIC assay to detect α‐synuclein aggregates in cerebrospinal fluid (CSF) of patients with suspected Creutzfeldt–Jakob disease who had a neuropathological diagnosis of dementia with Lewy bodies (DLB) (n = 7), other neurod
Externí odkaz:
https://doaj.org/article/f4deb6fe7ffd42969999bc511093e3f8
Autor:
Gianluigi Zanusso, Elisa Colaizzo, Anna Poleggi, Carlo Masullo, Raffaello Romeo, Sergio Ferrari, Matilde Bongianni, Michele Fiorini, Dorina Tiple, Luana Vaianella, Marco Sbriccoli, Flavia Porreca, Michele Equestre, Maurizio Pocchiari, Franco Cardone, Anna Ladogana
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 18, p 10210 (2022)
Genetic Creutzfeldt–Jakob disease (gCJD) associated with the V180I mutation in the prion protein (PrP) gene (PRNP) in phase with residue 129M is the most frequent cause of gCJD in East Asia, whereas it is quite uncommon in Caucasians. We report on
Externí odkaz:
https://doaj.org/article/d9c083d816cb4166ade3f9c43dd04b42
Autor:
Dorina Tiple, Anna Poleggi, Vittorio Mellina, Antonino Morocutti, Livia Brusa, Cesare Iani, Elisa Colaizzo, Luana Vaianella, Simone Baiardi, Anna Ladogana, Piero Parchi, Maurizio Pocchiari
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-4 (2019)
Externí odkaz:
https://doaj.org/article/5860a317bc2a45b3887bb8ac70eee5b7
Autor:
Andrea Mastrangelo, Simone Baiardi, Corrado Zenesini, Anna Poleggi, Angela Mammana, Barbara Polischi, Anna Ladogana, Sabina Capellari, Piero Parchi
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 13, Iss 1, Pp n/a-n/a (2021)
Abstract Introduction Surrogate cerebrospinal fluid (CSF) biomarkers of neurodegeneration still have a central role in the first‐line screening of patients with suspected Creutzfeldt‐Jakob disease (CJD). Recently, CSF α‐synuclein, a marker of
Externí odkaz:
https://doaj.org/article/cdff49935fca4b6db422b16da0ed4cd0
Autor:
Samir Abu-Rumeileh, Peggy Barschke, Patrick Oeckl, Simone Baiardi, Angela Mammana, Andrea Mastrangelo, Mhd Rami Al Shweiki, Petra Steinacker, Anna Ladogana, Sabina Capellari, Markus Otto, Piero Parchi
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 4, p 2051 (2022)
Proenkephalin (PENK) and prodynorphin (PDYN) are endogenous opioid peptides mainly produced in the striatum and, to a lesser extent, in the cerebral cortex. Dysregulated metabolism and altered cerebrospinal fluid (CSF) levels of PENK and PDYN have be
Externí odkaz:
https://doaj.org/article/25eb4a0d0c994a14942c4b51177cfe93
Autor:
Simone Baiardi, Angela Mammana, Marcello Rossi, Anna Ladogana, Benedetta Carlà, Pierluigi Gambetti, Sabina Capellari, Piero Parchi
Publikováno v:
Viruses, Vol 14, Iss 2, p 367 (2022)
Variably protease-sensitive prionopathy is an exceedingly rare, likely underestimated, sporadic prion disease that is characterized by heterogeneous and often non-specific clinical and pathological features posing diagnostic challenges. We report the
Externí odkaz:
https://doaj.org/article/65aacd78e1e84354bd42ee89b6691d43
Autor:
Samir Abu-Rumeileh, Sabina Capellari, Michelangelo Stanzani-Maserati, Barbara Polischi, Paolo Martinelli, Paola Caroppo, Anna Ladogana, Piero Parchi
Publikováno v:
Alzheimer’s Research & Therapy, Vol 10, Iss 1, Pp 1-11 (2018)
Abstract Background Neurofilament light chain protein (NfL) is a surrogate biomarker of neurodegeneration that has never been systematically tested, either alone or in combination with other biomarkers, in atypical/rapidly progressive neurodegenerati
Externí odkaz:
https://doaj.org/article/87c4548d8562420d999ab76bbb32159c