Zobrazeno 1 - 8
of 8
pro vyhledávání: '"cerebrospinal fluid [Prion Diseases]"'
Autor:
Llorens, Franc, Villar-Piqué, Anna, Hermann, Peter, Schmitz, Matthias, Calero, Olga, Stehmann, Christiane, Sarros, Shannon, Moda, Fabio, Ferrer, Isidre, Poleggi, Anna, Pocchiari, Maurizio, Catania, Marcella, Klotz, Sigrid, O'Regan, Carl, Brett, Francesca, Heffernan, Josephine, Ladogana, Anna, Collins, Steven J, Calero, Miguel, Kovacs, Gabor G, Zerr, Inga
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Biomolecules, Vol 10, Iss 2, p 290 (2020)
Biomolecules 10(2), 290 (2020). doi:10.3390/biom10020290
Biomolecules
Volume 10
Issue 2
Repisalud
Instituto de Salud Carlos III (ISCIII)
Universidad de Barcelona
Biomolecules, Vol 10, Iss 2, p 290 (2020)
Biomolecules 10(2), 290 (2020). doi:10.3390/biom10020290
Biomolecules
Volume 10
Issue 2
Repisalud
Instituto de Salud Carlos III (ISCIII)
Human prion diseases are classified into sporadic, genetic, and acquired forms. Within this last group, iatrogenic Creutzfeldt&ndash
Jakob disease (iCJD) is caused by human-to-human transmission through surgical and medical procedures. After rea
Jakob disease (iCJD) is caused by human-to-human transmission through surgical and medical procedures. After rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::881f9e30ba11bb50bfed9b0956c6a5b3
http://hdl.handle.net/2445/173289
http://hdl.handle.net/2445/173289
Autor:
Zerr, Inga, Villar-Piqué, Anna, Schmitz, Vanda Edit, Poleggi, Anna, Pocchiari, Maurizio, Sánchez-Valle, Raquel, Calero, Miguel, Calero, Olga, Baldeiras, Inês, Santana, Isabel, Kovacs, Gabor G., Llorens, Franc, Schmitz, Matthias
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Biomolecules
Repisalud
Instituto de Salud Carlos III (ISCIII)
Biomolecules 9(12), 800 (2019). doi:10.3390/biom9120800
Volume 9
Issue 12
Universidad de Barcelona
Biomolecules
Repisalud
Instituto de Salud Carlos III (ISCIII)
Biomolecules 9(12), 800 (2019). doi:10.3390/biom9120800
Volume 9
Issue 12
The exploration of accurate diagnostic markers for differential diagnosis of neurodegenerative diseases is an ongoing topic. A previous study on cerebrospinal fluid (CSF)-mitochondrial malate dehydrogenase 1 (MDH1) in sporadic Creutzfeldt&ndash
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a1786b341a1ed3ce879f1e4aeb77f85d
http://hdl.handle.net/2445/167999
http://hdl.handle.net/2445/167999
Autor:
Saima Zafar, Anna Villar-Piqué, Hermann C. Altmeppen, Matthias Schmitz, Franc Llorens, Katrin Thüne, Inga Zerr, Markus Glatzel, Markus Schlomm
Publikováno v:
Expert review of molecular diagnostics 19(11), 1007-1018 (2019). doi:10.1080/14737159.2019.1667231
Introduction: Human prion diseases are a heterogeneous group of incurable and debilitating conditions characterized by a progressive degeneration of the central nervous system. The conformational changes of the cellular prion protein and its formatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7f6f5688ca2d018f4afb353222ae78b
https://pubmed.ncbi.nlm.nih.gov/31512940
https://pubmed.ncbi.nlm.nih.gov/31512940
Autor:
Shannon Sarros, Isidre Ferrer, Inês Baldeiras, Isabel Santana, Franc Llorens, Christiane Stehmann, Matthias Schmitz, Anna Villar-Piqué, Miguel Calero, Olga Calero, Raquel Sánchez-Valle, Michael D. Geschwind, Ingolf Lachmann, Anna Poleggi, André Karch, Eva Mitrova, Inga Zerr, Maurizio Pocchiari, Anna Ladogana, Dana Žáková, Steven J. Collins
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Molecular neurobiology 56(4), 2811-2821 (2018). doi:10.1007/s12035-018-1251-1
Recercat. Dipósit de la Recerca de Catalunya
instname
Molecular neurobiology
Universidad de Barcelona
Molecular neurobiology 56(4), 2811-2821 (2018). doi:10.1007/s12035-018-1251-1
Recercat. Dipósit de la Recerca de Catalunya
instname
Molecular neurobiology
Cerebrospinal fluid (CSF) total prion protein (t-PrP) is decreased in sporadic Creutzfeldt-Jakob disease (sCJD). However, data on the comparative signatures of t-PrP across the spectrum of prion diseases, longitudinal changes during disease progressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::190592be13de9a3b24a376660a2223af
https://pubmed.ncbi.nlm.nih.gov/30062673
https://pubmed.ncbi.nlm.nih.gov/30062673
Autor:
Bradley R. Groveman, Saima Zafar, Inga Zerr, Maria Cramm, Dominik Müller-Cramm, Byron Caughey, Christina D. Orrú, Katsuya Satoh, Steven J. Collins, Walter J. Schulz-Schaeffer, Franc Llorens, Ryuichiro Atarashi, Matthias Schmitz
Publikováno v:
Nature protocols 11(11), 2233-2242 (2016). doi:10.1038/nprot.2016.120
The development and adaption of in vitro misfolded protein amplification systems has been a major innovation in the detection of abnormally folded prion protein scrapie (PrPSc) in human brain and cerebrospinal fluid (CSF) samples. Herein, we describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdbd203fbae5a814dee7624d862b8df7
https://pubmed.ncbi.nlm.nih.gov/27735933
https://pubmed.ncbi.nlm.nih.gov/27735933
Autor:
Saima Zafar, Katharina Lüllmann, Panteleimon Oikonomou, Elisabeth Ebert, Michael Beekes, Markus Schlomm, Matthias Schmitz, Inga Zerr, Marie Wohlhage, Eva Mitrova
Publikováno v:
Neurobiology of Aging
Neurobiology of aging 35(5), 1177-1188 (2014). doi:10.1016/j.neurobiolaging.2013.11.010
Neurobiology of aging 35(5), 1177-1188 (2014). doi:10.1016/j.neurobiolaging.2013.11.010
The present study investigates whether posttranslational modifications of cellular prion protein (PrP(C)) in the cerebrospinal fluid (CSF) of humans with prion diseases are associated with methionine (M) and/or valine (V) polymorphism at codon 129 of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a8e12b295f55297b0a4e0711a12dbbd
https://pubmed.ncbi.nlm.nih.gov/24360565
https://pubmed.ncbi.nlm.nih.gov/24360565
Autor:
Saima Zafar, Franziska Kuhn, Maria Cramm, André Karch, Daniela Varges, Alex Raeber, Inga Zerr, Matthias Schmitz, Eva Mitrova, Bjoern Schroeder
Publikováno v:
Molecular Neurobiology
Molecular neurobiology 51(1), 396-405 (2014). doi:10.1007/s12035-014-8709-6
Molecular neurobiology 51(1), 396-405 (2014). doi:10.1007/s12035-014-8709-6
The development of in vitro amplification systems allows detecting femtomolar amounts of prion protein scrapie (PrPSc) in human cerebrospinal fluid (CSF). We performed a CSF study to determine the effects of prion disease type, codon 129 genotype, Pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4260722048d347da6900228834c46f9
Autor:
Beata Sikorska, Anna Ladogana, Isabel Santana, Pawel P. Liberski, Stefan Goebel, Kaj Blennow, Daniela Varges, Aikaterini Karsanidou, Eirini Kanata, Theodoros Sklaviadis, André Karch, Inês Baldeiras, Isidro Ferrer, Daniela Diaz-Lucena, Franc Llorens, Inga Zerr, Ewa Golanska, Tobias Knipper, Raquel Sánchez-Valle, Matthias Schmitz, Peter Hermann, Henrik Zetterberg, Anna Villar-Piqué, Miguel Calero, Olga Calero
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Alzheimer's and dementia 14(6), 751-763 (2018). doi:10.1016/j.jalz.2017.12.008
Alzheimer's & Dementia
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Alzheimer's and dementia 14(6), 751-763 (2018). doi:10.1016/j.jalz.2017.12.008
Alzheimer's & Dementia
Introduction Neurofilament light (NFL) levels in the cerebrospinal fluid are increased in several neurodegenerative dementias. However, their diagnostic accuracy in the differential diagnostic context is unknown. Methods Cerebrospinal fluid NFL level
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd641d4a66e22a41176ed74e23d0128a
http://hdl.handle.net/2445/137381
http://hdl.handle.net/2445/137381