Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Vittorio Mellina"'
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:
Italia La Rosa, Francesco Diana, Claudio Colonnese, Simone Peschillo, Paolo Missori, Francesco Marzetti, Vittorio Mellina
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 26:2082-2086
Background Intracerebral hemorrhage can be classified as either primary or secondary to various conditions such as vascular anomalies or stroke. We present a case of real-time incident detected on digital subtraction angiography (DSA) during thrombec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::945cb932f5c301744447f53eec70f7eb
https://doi.org/10.1016/j.jstrokecerebrovasdis.2017.04.026
https://doi.org/10.1016/j.jstrokecerebrovasdis.2017.04.026
Autor:
Maurizio Pocchiari, Vittorio Mellina, Luana Vaianella, Antonino Morocutti, Dorina Tiple, Simone Baiardi, Elisa Colaizzo, Anna Ladogana, Piero Parchi, Livia Brusa, Anna Poleggi, Cesare Iani
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-4 (2019)
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-4 (2019)
Genetic transmissible spongiform encephalopathy (TSE) diseases are always associated with one of the more than 50 disease-associated point or insert mutations of the PrP gene (PRNP) [12] and represent approximately 10 to 20% of all forms of TSE disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b45664cb92c28e29b7627d0be039271
https://doi.org/10.1186/s40478-019-0699-1
https://doi.org/10.1186/s40478-019-0699-1
Autor:
Anna Poleggi, Anna Ladogana, Ramona Vinci, Serena Principe, Piero Parchi, Sabina Capellari, Maria Eugenia Schininà, S. Almonti, Roberta Galeno, Vittorio Mellina, Bruno Maras, Franco Cardone, Laura Di Francesco, Silvio Notari, Maurizio Pocchiari
Publikováno v:
Biochemical and Biophysical Research Communications. 454:289-294
Creutzfeldt-Jakob disease (CJD) is a neurodegenerative disorder characterized by the deposition of the pathological conformer (PrP(CJD)) of the host encoded cellular prion protein (PrP(C)). In genetic CJD associated with V210I or R208H PrP substituti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::652278343fe8d27763d3a5df09ce5b8b
https://doi.org/10.1016/j.bbrc.2014.10.051
https://doi.org/10.1016/j.bbrc.2014.10.051
Autor:
Vittorio Mellina, J.-P. Brandel, Bettina Meissner, S. Almonti, Inga Zerr, Patrick Cras, Robert G. Will, Gerard H. Jansen, D. Collie, Steven J. Collins, Michael B. Coulthart, David Summers, B. Van Everbroeck, Kai Kallenberg, Damien Galanaud, Pascual Sánchez-Juan, Pete Smith, H. Roberts
Publikováno v:
Neurology
Neurology, 2009, 72 (23), pp.1994-2001. ⟨10.1212/WNL.0b013e3181a96e5d⟩
Neurology, American Academy of Neurology, 2009, 72 (23), pp.1994-2001. ⟨10.1212/WNL.0b013e3181a96e5d⟩
Neurology, 2009, 72 (23), pp.1994-2001. ⟨10.1212/WNL.0b013e3181a96e5d⟩
Neurology, American Academy of Neurology, 2009, 72 (23), pp.1994-2001. ⟨10.1212/WNL.0b013e3181a96e5d⟩
International audience; BACKGROUND: With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six molecular subtypes (MM1, MM2, MV1, MV2, VV1, and VV2) have been described, which vary with respect to age at disease onset, disease duration, early sym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db6a8841f31bd16d034a83bdf0ed6574
https://hal.inria.fr/hal-00805400
https://hal.inria.fr/hal-00805400
Autor:
K. Kallenberg, Bettina Meissner, Patrick Cras, Gerard H. Jansen, Vittorio Mellina, Steven J. Collins, D Galanaud, I. Zerr, JP Brandel, Robert G. Will, David Summers, Pascual Sánchez-Juan
Publikováno v:
RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 181
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fde028edd9e3679abfd0c5786a9c9bd
https://doi.org/10.1055/s-0029-1221369
https://doi.org/10.1055/s-0029-1221369
Autor:
Anna Ladogana, Miguel Calero, N. Cuadrado-Corrales, Uta Heinemann, Eva Mitrova, C.M. van Duijn, Pascual Sánchez-Juan, Albert Saiz, Dana Slivarichova, Alison Green, Vittorio Mellina, Theodoros Sklaviadis, Katharina Stoeck, Jerzy Kulczycki, K Hess, Raquel Sánchez-Valle, Richard Knight, Inga Zerr
Publikováno v:
European Journal of Neurology, 14(2), 121-124. Wiley-Blackwell Publishing Ltd
Patients with suspected Creutzfeldt-Jakob disease (CJD) often have routine cerebrospinal fluid (CSF) analysis performed to exclude treatable inflammatory conditions; however, little information is available about the range of results obtained for CSF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65075317a6ad3aa656dc36fad66cf137
https://pubmed.ncbi.nlm.nih.gov/17250717
https://pubmed.ncbi.nlm.nih.gov/17250717
Autor:
Victoria Lewis, Katharina Stoeck, Markus Glatzel, Vittorio Mellina, Pascual Sánchez-Juan, Steven J. Collins, Jean-Philippe Brandel, Inga Zerr, N. Delasnerie-Laupretre, Javier Almazán, Jesús de Pedro-Cuesta, Cornelia M. van Duijn, Gerard H. Jansen, Herbert Budka, Ellen Gelpi, Michael B. Coulthart, Maurizio Pocchiari, Hans A Kretszchmar, Annick Alpérovitch, Maria Puopolo, Eva Mitrova
Publikováno v:
Repisalud
Instituto de Salud Carlos III (ISCIII)
BMC Public Health
BMC Public Health, BioMed Central, 2006, 6, pp.278. ⟨10.1186/1471-2458-6-278⟩
BMC Public Health, 2006, 6, pp.278. ⟨10.1186/1471-2458-6-278⟩
BMC Public Health, Vol 6, Iss 1, p 278 (2006)
BMC Public Health, 6. BioMed Central Ltd.
Instituto de Salud Carlos III (ISCIII)
BMC Public Health
BMC Public Health, BioMed Central, 2006, 6, pp.278. ⟨10.1186/1471-2458-6-278⟩
BMC Public Health, 2006, 6, pp.278. ⟨10.1186/1471-2458-6-278⟩
BMC Public Health, Vol 6, Iss 1, p 278 (2006)
BMC Public Health, 6. BioMed Central Ltd.
Background The objective of this study was to describe the diagnostic panorama of human transmissible spongiform encephalopathies across 11 countries. Methods From data collected for surveillance purposes, we describe annual proportions of deaths due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7586a27ad6ea67ffb0449842bf5b7fb4
https://doi.org/10.1186/1471-2458-6-278
https://doi.org/10.1186/1471-2458-6-278
Autor:
S. Almonti, Anna Poleggi, Michele Equestre, Maurizio Pocchiari, Anna Ladogana, Maria Puopolo, Vittorio Mellina
Publikováno v:
Neurology. 64(9)
Objective: To assess the incidence and mortality rates of genetic transmissible spongiform encephalopathy (TSE) diseases in Italy. Methods: The authors have sequenced the prion protein gene ( PRNP ) in 643 patients referred to the Italian Registry of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12859d7d9f1de4852df7ddc283e98038
https://pubmed.ncbi.nlm.nih.gov/15883322
https://pubmed.ncbi.nlm.nih.gov/15883322