Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Zita Jobbágy"'
Autor:
Cecilia Rajda, Csilla Rózsa, Andrea Mike, Gábor Lovas, Zsolt Mezei, Gábor Jakab, Péter Ács, Gábor Rum, Magdolna Simó, Zita Jobbágy, Zita Bíró, Anita Trauninger, Piroska Imre, Klotild Mátyás, István Deme, Zsolt Illés, Tunde Csepany
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-8 (2023)
Abstract Multiple sclerosis (MS) may impact quality of life, careers and family plans of the affected individuals. The current treatments with disease modifying therapies aim to prevent people with MS (pwMS) from disability accumulation and progressi
Externí odkaz:
https://doaj.org/article/be59c2447b67412d8c543f4314d3ae5c
Autor:
Zsófia Kokas, Dániel Sandi, Zsanett Fricska-Nagy, Judit Füvesi, Tamás Biernacki, Ágnes Köves, Ferenc Fazekas, Adrienne Jóri Birkás, Gabriella Katona, Krisztina Kovács, Dániel Milanovich, Enikő Dobos, István Kapás, Gábor Jakab, Tünde Csépány, Erzsébet Bense, Klotild Mátyás, Gábor Rum, Zoltán Szolnoki, István Deme, Zita Jobbágy, Dávid Kriston, Zsuzsanna Gerócs, Péter Diószeghy, László Bors, Adrián Varga, Levente Kerényi, Gabriella Molnár, Piroska Kristóf, Zsuzsanna Ágnes Nagy, Mária Sátori, Piroska Imre, Szilvia Péntek, Péter Klivényi, Zsigmond Tamás Kincses, László Vécsei, Krisztina Bencsik
Publikováno v:
PLoS ONE, Vol 17, Iss 3 (2022)
A patients Because of the past 3 decades’ extensive research, several disease modifying therapies became available, thus a paradigm change is multiple sclerosis care was necessary. In 2018 a therapeutic guideline was created recommending that treat
Externí odkaz:
https://doaj.org/article/b74f88ce35424d3a83206f1e4beda0ee
Autor:
Krisztina Bencsik, Enikő Dobos, Zita Jobbágy, Adrienne Jóri Birkás, Krisztina Kovács, Mária Sátori, Gyula Lencsés, Gabor Bartok, Erika Losonczi, László Vécsei, on behalf of the Teri-REAL Investigators
Publikováno v:
Pharmaceuticals, Vol 15, Iss 5, p 598 (2022)
Relapsing-remitting multiple sclerosis (RRMS) is a degenerative, inflammatory disease of the central nervous system in which symptoms and disability progression vary significantly among patients. Teri-REAL was a prospective, real-world observational
Externí odkaz:
https://doaj.org/article/b2af7af885ae4160a1161d3df55a5068
Autor:
Investigators, Krisztina Bencsik, Enikő Dobos, Zita Jobbágy, Adrienne Jóri Birkás, Krisztina Kovács, Mária Sátori, Gyula Lencsés, Gabor Bartok, Erika Losonczi, László Vécsei, on behalf of the Teri-REAL Investigators on behalf of the Teri-REAL
Publikováno v:
Pharmaceuticals; Volume 15; Issue 5; Pages: 598
Relapsing-remitting multiple sclerosis (RRMS) is a degenerative, inflammatory disease of the central nervous system in which symptoms and disability progression vary significantly among patients. Teri-REAL was a prospective, real-world observational
Autor:
Mária Judit Molnár, Katalin Visy Várdi, Zoltán Grosz, Levente Kerényi, Lívia Dézsi, Laszló Jávor, Zsuzsanna Almássy, Ágnes Sebők, Beata Borsos, Zita Jobbágy, Judit Bidló
Publikováno v:
Ideggyógyászati szemle. 73:151-159
Pompe disease (PD) is a rare lysosomal disease caused by the deficient activity of acid alpha-glucosidase (GAA) enzyme due to mutations in the GAA gene. The enzymatic deficiency leads to the accumulation of glycogen within the lysosomes. Clinically,
Autor:
Zita Jobbágy, Lívia Dézsi, Veronika Harmath, Agnes Herczegfalvi, Ildikó Szatmári, Anikó Gál, Beata Borsos, Zsuzsanna Almássy, Levente Kerényi, Zoltán Grosz, Katalin Szakszon, Eniko Balku, Mária Judit Molnár, Laszló Jávor, Ágnes Sebők
Publikováno v:
Life, Vol 11, Iss 507, p 507 (2021)
Life
Volume 11
Issue 6
Life
Volume 11
Issue 6
Pompe disease is caused by the accumulation of glycogen in the lysosomes due to a deficiency of the lysosomal acid-α-glucosidase (GAA) enzyme. Depending on residual enzyme activity, the disease manifests two distinct phenotypes. In this study, we as
Autor:
Mária Judit, Molnár, Beáta, Borsos, Katalin Visy, Várdi, Zoltán, Grosz, Ágnes, Sebők, Lívia, Dézsi, Zsuzsanna, Almássy, Levente, Kerényi, Zita, Jobbágy, László, Jávor, Judit, Bidló
Publikováno v:
Ideggyogyaszati szemle. 73(05-06)
Pompe disease (PD) is a rare lysosomal disease caused by the deficient activity of acid alpha-glucosidase (GAA) enzyme due to mutations in the GAA gene. The enzymatic deficiency leads to the accumulation of glycogen within the lysosomes. Clinically,
Autor:
László Horváth, Gabriella Molnár, Péter Ács, Viktoria Papp, Judit Kasza, Zsolt Illes, László Vécsei, Adrienne Jóri Birkás, Csilla Rozsa, Gábor Lovas, Thor Petersen, Levente Kerényi, István Deme, Mária Sátori, Gábor Jakab, Zsuzsanna Lohner, Krisztina Bencsik, Piroska Imre, Melinda Magyari, Gyöngyi Galántai, Gábor Rum, Ágnes Köves, Ferenc Nagy, Krisztina Kovacs, Cecilia Rajda, Magdolna Simó, Anna Iljicsov, Zsuzsanna Nagy, Zita Jobbágy, Péter Diószeghy, Timea Berki, Nils Koch-Henriksen, Sámuel Komoly
Publikováno v:
Papp, V, Iljicsov, A, Rajda, C, Magyari, M, Koch-Henriksen, N, Petersen, T, Jakab, G, Deme, I, Nagy, F, Imre, P, Lohner, Z, Kovács, K, Birkás, A J, Köves, Rum, G, Nagy, Z, Kerényi, L, Vécsei, L, Bencsik, K, Jobbágy, Z, Diószeghy, P, Horváth, L, Galántai, G, Kasza, J, Molnár, G, Simó, M, Sátori, M, Rózsa, C, Ács, P, Berki, T, Lovas, G, Komoly, S & Illes, Z 2020, ' A population-based epidemiological study of neuromyelitis optica spectrum disorder in Hungary ', European Journal of Neurology, vol. 27, no. 2, pp. 308-317 . https://doi.org/10.1111/ene.14079
Background and purpose: The goal of this study was to determine the prevalence and incidence of neuromyelitis optica spectrum disorder (NMOSD) in Hungary based on the 2015 International Panel of NMO Diagnosis (IPND) criteria. Methods: A retrospective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec270552c6eb5b7401fc8e643712fba9
https://pure.au.dk/portal/da/publications/a-populationbased-epidemiological-study-of-neuromyelitis-optica-spectrum-disorder-in-hungary(b01946d5-1cef-43d4-b137-26dc5f3fc844).html
https://pure.au.dk/portal/da/publications/a-populationbased-epidemiological-study-of-neuromyelitis-optica-spectrum-disorder-in-hungary(b01946d5-1cef-43d4-b137-26dc5f3fc844).html
Autor:
Sámuel Komoly, Zsanett Fricska-Nagy, László Vécsei, Krisztina Bencsik, Csilla Rozsa, Judit Füvesi, Gyula Lencsés, Gábor Jakab, Zita Jobbágy, Tünde Csépány
Background The common symptoms of multiple sclerosis are fatigue, depression, cognitive dysfunction, pain and sexual dysfunction, which influence the health-related quality of life of the patients. Objective We aimed to determine the correlations bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38eaaae5466c11f32446bebe93ee417e
Autor:
Csilla Rozsa, George Füst, Zsolt Illes, Lilian Varga, Zsuzsanna Nagy, Kornélia Eizler, Nóra Veszeli, Anita Trauninger, Zoltán Prohászka, Dorottya Csuka, Zita Jobbágy
Publikováno v:
Immunobiology. 217:1216