Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Jerzy Kulczycki"'
Autor:
David S. Park, Matthew P. Mount, Steve M. Callaghan, Mandana Amini, Jerzy Kulczycki, Zixu Mao, Yi Zhang, Ruth S. Slack, Hymie Anisman
Publikováno v:
Journal of Biological Chemistry. 288:14362-14371
We have earlier reported the critical nature of calpain-CDK5-MEF2 signaling in governing dopaminergic neuronal loss in vivo. CDK5 mediates phosphorylation of the neuronal survival factor myocyte enhancer factor 2 (MEF2) leading to its inactivation an
Autor:
Szpak Gm, Walentyna Szirkowiec, Wioletta Krysa, Jerzy Kulczycki, Janusz Zimowski, Jacek Zaremba, Wanda Łojkowska, Anna Limon-Sztencel
Publikováno v:
Neurologia i Neurochirurgia Polska. 46:509-518
Background and purpose The aim of the study was to perform molecular analysis in a group of patients affected with prion disease. Diagnosis was based on results of clinical and/or histopathological examination of the brain. This is the largest invest
Publikováno v:
Journal of Biological Chemistry. 286:28783-28793
Although there is growing evidence for a role of the innate immune response in Parkinson's disease, the nature of any humoral response in dopaminergic degeneration is uncertain. Here we report on a protracted N-methyl-4-phenyl-1,2,3,6-tetrahydropyrid
Autor:
Monika Rudzińska, Christian Beetz, Marta Rajkiewicz, Iwona Stepniak, Katarzyna Kurdziel, Maria Rakowicz, Ewelina Elert-Dobkowska, Wioletta Krysa, Anna Sobanska, Jerzy Kulczycki, Anna Sulek, Wanda Lipczynska-Lojkowska, Anna Wasielewska, Jolanta Kubalska, Jacek Zaremba, Agata Sikorska, Jacek Pilch
Publikováno v:
Journal of the neurological sciences. 359(1-2)
Hereditary spastic paraplegias (HSPs) consist of a heterogeneous group of genetically determined neurodegenerative disorders. Progressive lower extremity weakness and spasticity are the prominent features of HSPs resulting from retrograde axonal dege
Publikováno v:
Neurologia i Neurochirurgia Polska. 45:611-613
Autor:
Jerzy Kulczycki
Publikováno v:
Neurologia i Neurochirurgia Polska. 44:614-616
Autor:
Jean-Louis Laplanche, Katell Peoc'h, Cornelia M. van Duijn, Miguel Calero, Gabi Schelzke, Anna Ladogana, Alison Green, André Karch, Katharina Stoeck, Pascual Sánchez-Juan, Raquel Sánchez-Valle, Richard Knight, Joanna Gawinecka, Dana Slivarichova, Maurizio Pocchiari, Jerzy Kulczycki, Inga Zerr, Theodor Sklaviadis, Albert Saiz, Adriano Aguzzi, Eva Mitrova
Publikováno v:
Stoeck, K, Sanchez-Juan, P, Gawinecka, J, Green, A, Ladogana, A, Pocchiari, M, Sanchez-Valle, R, Mitrova, E, Sklaviadis, T, Kulczycki, J, Slivarichova, D, Saiz, A, Calero, M, Knight, R, Aguzzi, A, Laplanche, J-L, Peoc'h, K, Schelzke, G, Karch, A, van Duijn, C M & Zerr, I 2012, ' Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias : a longitudinal multicentre study over 10 years ', Brain, vol. 135, no. 10, pp. 3051-3061 . https://doi.org/10.1093/brain/aws238
Brain, 135, 3051-3061. Oxford University Press
Brain
Brain, 135, 3051-3061. Oxford University Press
Brain
To date, cerebrospinal fluid analysis, particularly protein 14-3-3 testing, presents an important approach in the identification of Creutzfeldt–Jakob disease cases. However, one special point of criticism of 14-3-3 testing is the specificity in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e42ee7665ee4a84ecccb8b372a67008
http://resolver.sub.uni-goettingen.de/purl?gs-1/8382
http://resolver.sub.uni-goettingen.de/purl?gs-1/8382
Autor:
Pascual Sánchez-Juan, N. Cuadrado-Corrales, Anna Ladogana, Albert Saiz, Theodoros Sklaviadis, Eva Mitrova, Richard Knight, Silvia Koščová, Raquel Sánchez-Valle, Joanna Gawinecka, Inga Zerr, Jerzy Kulczycki, Miguel Calero, Alison Green, Adriano Aguzzi, Maurizio Pocchiari, Cornelia M. van Duijn
Publikováno v:
Ladogana, A, Sanchez-Juan, P, Mitrova, E, Green, A, Cuadrado-Corrales, N, Sanchez-Valle, R, Koscova, S, Aguzzi, A, Sklaviadis, T, Kulczycki, J, Gawinecka, J, Saiz, A, Calero, M, van Duijn, C M, Pocchiari, M, Knight, R & Zerr, I 2009, ' Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies ', Journal of Neurology, vol. 256, no. 10, pp. 1620-1628 . https://doi.org/10.1007/s00415-009-5163-x
Journal of Neurology
Journal of Neurology, 256(10), 1620-1628. D. Steinkopff-Verlag
Journal of Neurology
Journal of Neurology, 256(10), 1620-1628. D. Steinkopff-Verlag
The 14-3-3 protein test has been shown to support the clinical diagnosis of sporadic Creutzfeldt-Jakob disease (CJD) when associated with an adequate clinical context, and a high differential potential for the diagnosis of sporadic CJD has been attri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32f0010436cd328cd01c8957593ef63
http://resolver.sub.uni-goettingen.de/purl?gs-1/6745
http://resolver.sub.uni-goettingen.de/purl?gs-1/6745
Autor:
Grazyna M, Szpak, Eliza, Lewandowska, Bogna, Schmidt-Sidor, Elzbieta, Pasennik, Joanna, Modzelewska, Tomasz, Stepień, Grzegorz, Zdaniuk, Jerzy, Kulczycki, Teresa, Wierzba-Bobrowicz
Publikováno v:
Folia neuropathologica. 46(3)
This report presents a case of widespread intramedullary giant cell ependymoma arising from the central canal of the C4 segment of the spinal cord in a 28-year-old man admitted to hospital with tetraplegia and signs of increased intracranial pressure
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