Klivényi Péter (Peter Klivenyi, Péter Klivényi)

Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 24

Top Topics

Prognostic Factors

Multiple Sclerosis

Top Venues

Ideggyogyaszati szemle

International journal of molecular sciences

Research square

This page only lists publications with an associated author ORCID identifier.

Publications

Miriama Ostrozovicova, Gertrud Tamas, Petr Dušek, Milan Grofik, Vladimir Han, Petr Holly, Robert Jech, Katarina Kalinova, Klivényi Péter, Norbert Kovacs, Kristina Kulcsarova, Egon Kurca, Alexandra Lackova, Hamin Lee, Patrick Lewis, Veronika Magocova, Maria Marekova, David Murphy, Jan Necpal, David Pinter, Miroslava Rabajdova, Evžen Růžička, Tereza Serranova, Katarzyna Smilowska, Krisztina Soos, Igor Straka, Tatiana Svorenova, Peter Valkovic, Katerina Zarubova, Zuzana Gdovinová, Henry Houlden, Mie Rizig, Matei Skorvanek
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central Europe. Research square (2024)
Miriama Ostrozovicova, Gertrud Tamas, Petr Dušek, Milan Grofik, Vladimir Han, Petr Holly, Robert Jech, Katarina Kalinova, Klivényi Péter, Norbert Kovacs, Kristina Kulcsarova, Egon Kurca, Alexandra Lackova, Hamin Lee, Patrick Lewis, Veronika Magocova, Maria Marekova, David Murphy, Jan Necpal, David Pinter, Miroslava Rabajdova, Evžen Růžička, Tereza Serranova, Katarzyna Smilowska, Krisztina Soos, Igor Straka, Tatiana Svorenova, Peter Valkovic, Katerina Zarubova, Zuzana Gdovinová, Henry Houlden, Mie Rizig, Matei Skorvanek
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central Europe. Research square (2024)
Miriama Ostrozovicova, Gertrud Tamas, Petr Dušek, Milan Grofik, Vladimir Han, Petr Holly, Robert Jech, Katarina Kalinova, Klivényi Péter, Norbert Kovacs, Kristina Kulcsarova, Egon Kurca, Alexandra Lackova, Hamin Lee, Patrick Lewis, Veronika Magocova, Maria Marekova, David Murphy, Jan Necpal, David Pinter, Miroslava Rabajdova, Evžen Růžička, Tereza Serranova, Katarzyna Smilowska, Krisztina Soos, Igor Straka, Tatiana Svorenova, Peter Valkovic, Katerina Zarubova, Zuzana Gdovinová, Henry Houlden, Mie Rizig, Matei Skorvanek
p.L1795F LRRK2 variant is a common cause of Parkinson's disease in Central Europe. Research square (2024)
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Zádori Dénes, Salamon András, Judit Danis, Kalmár Tibor, Zoltán Maróti, Mária Judit Molnár, Klivényi Péter, Márta Széll, Éva Ádám
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International journal of molecular sciences 24 (3) (2023)
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Zádori Dénes, Salamon András, Judit Danis, Kalmár Tibor, Zoltán Maróti, Mária Judit Molnár, Klivényi Péter, Márta Széll, Éva Ádám
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International journal of molecular sciences 24 (3) (2023)
Faragó Péter, Zsigmond Tamás Kincses, Kovács László, Hortobágyi Tibor, Despotov Katalin, Radics Bence, Klivényi Péter, János Tajti
[Isolated IgG4 hypertrophic pachymeningitis with cranial nerve involvement]. Ideggyogyaszati szemle 76 (1-2) (2023)
Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, Azlina Ahmad-Annuar, Bashayer R Al-Mubarak, Roy N Alcalay, Victoria Alvarez, Ignacio Amorin, Grazia Annesi, David Arkadir, Soraya Bardien, Roger A Barker, Melinda Barkhuizen, A Nazli Basak, Vincenzo Bonifati, Agnita Boon, Laura Brighina, Kathrin Brockmann, Andrea Carmine Belin, Jonathan Carr, Jordi Clarimon, Mario Cornejo-Olivas, Leonor Correia Guedes, Jean-Christophe Corvol, David Crosiers, Joana Damásio, Parimal Das, Patricia de Carvalho Aguiar, Anna De Rosa, Jolanta Dorszewska, Sibel Ertan, Rosangela Ferese, Joaquim Ferreira, Emilia Gatto, Gençer Genç, Nir Giladi, Pilar Gómez-Garre, Hasmet Hanagasi, Nobutaka Hattori, Faycal Hentati, Dorota Hoffman-Zacharska, Sergey N Illarioshkin, Joseph Jankovic, Silvia Jesús, Valtteri Kaasinen, Anneke Kievit, Klivényi Péter, Vladimir Kostic, Dariusz Koziorowski, Andrea A Kühn, Anthony E Lang, Shen-Yang Lim, Chin-Hsien Lin, Katja Lohmann, Vladana Markovic, Mika Henrik Martikainen, George Mellick, Marcelo Merello, Lukasz M Milanowski, Pablo Mir, Özgür Öztop-Çakmak, Márcia Mattos Gonçalves Pimentel, Teeratorn Pulkes, Andreas Puschmann, Ekaterina Rogaeva, Esther M Sammler, Maria Skaalum Petersen, Matej Skorvanek, Mariana Spitz, Oksana Suchowersky, Ai Huey Tan, Pichet Termsarasab, Avner Thaler, Vitor Tumas, Enza Maria Valente, Bart van de Warrenburg, Caroline H Williams-Gray, Ruey-Mei Wu, Baorong Zhang, Alexander Zimprich, Justin Solle, Shalini Padmanabhan, Christine Klein
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project. PloS one 18 (10) (2023)
Salamon András, Zsófia Flóra Nagy, Margit Pál, Máté Szabó, Ádám Csősz, László Szpisjak, Gabriella Gárdián, Zádori Dénes, Márta Széll, Klivényi Péter
Genetic Screening of a Hungarian Cohort with Focal Dystonia Identified Several Novel Putative Pathogenic Gene Variants. International journal of molecular sciences 24 (13) (2023)
Faragó Péter, Zsigmond Tamás Kincses, Kovács László, Hortobágyi Tibor, Despotov Katalin, Radics Bence, Klivényi Péter, János Tajti
[Isolated IgG4 hypertrophic pachymeningitis with cranial nerve involvement]. Ideggyogyaszati szemle 76 (1-2) (2023)
Anett Csáti, Délia Szok, Rita Végh, Katalin Jakab, Károly Péter Sárvári, Gabriella Terhes, Gyula Pásztor, Magdolna Gaál, Klivényi Péter, János Tajti
[Neurosyphilis or not - a case of a differential diagnostic challenge]. Ideggyogyaszati szemle 76 (9-10) (2023)
Máté Szabó, Dániel DO Kiem, Gabriella Gárdián, Szpisjak László, Salamon András, Klivényi Péter, Zádori Dénes
Clinical features of cervical dystonia patients classified by the COL-CAP concept and treated with ultrasound-guided botulinum neurotoxin. Ideggyogyaszati szemle 76 (1-2) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Zsófia Flóra Nagy, Balázs Sonkodi, Margit Pál, Klivényi Péter, Márta Széll
Likely Pathogenic Variants of Ca v 1.3 and Na v 1.1 Encoding Genes in Amyotrophic Lateral Sclerosis Could Elucidate the Dysregulated Pain Pathways. Biomedicines 11 (3) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Zsófia Flóra Nagy, Balázs Sonkodi, Margit Pál, Klivényi Péter, Márta Széll
Likely Pathogenic Variants of Ca v 1.3 and Na v 1.1 Encoding Genes in Amyotrophic Lateral Sclerosis Could Elucidate the Dysregulated Pain Pathways. Biomedicines 11 (3) (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Levente Szalardy, Bernadett Fakan, Rita Maszlag-Torok, Emil Ferencz, Zita Reisz, Bence L Radics, Sandor Csizmadia, Laszlo Szpisjak, Adam Annus, Denes Zadori, Gábor G Kovács, Klivényi Péter
Identifying diagnostic and prognostic factors in cerebral amyloid angiopathy-related inflammation: a systematic analysis of published and seven new cases. Neuropathology and applied neurobiology (2023)
Klivényi Péter, Szpisjak László, Salamon András, Viola Luca Németh, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Dénes
[Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle 76 (1-2) (2023)
Fanni Annamária Boros, László Szpisjak, Renáta Bozó, Evelyn Kelemen, Zádori Dénes, Salamon András, Judit Danis, Kalmár Tibor, Zoltán Maróti, Mária Judit Molnár, Klivényi Péter, Márta Széll, Éva Ádám
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the CCDC88C Gene. International journal of molecular sciences 24 (3) (2023)
Dániel Sandi, Zsófia Kokas, Tamás Biernacki, Krisztina Bencsik, Klivényi Péter, László Vécsei
Proteomics in Multiple Sclerosis: The Perspective of the Clinician. International journal of molecular sciences 23 (9) (2022)
Levente Hadady, Klivényi Péter, Daniel Fabo, Sándor Beniczky
Real-world user experience with seizure detection wearable devices in the home environment. Epilepsia (2022)
Tamás Biernacki, Zsófia Kokas, Dániel Sandi, Judit Füvesi, Zsanett Fricska-Nagy, Péter Faragó, Tamás Zsigmond Kincses, Klivényi Péter, Krisztina Bencsik, László Vécsei
Emerging Biomarkers of Multiple Sclerosis in the Blood and the CSF: A Focus on Neurofilaments and Therapeutic Considerations. International journal of molecular sciences 23 (6) (2022)
Laszlo Szpisjak, Viola L Nemeth, Noemi Szepfalusi, Denes Zadori, Zoltan Maroti, Tibor Kalmar, Laszlo Vecsei, Klivényi Péter
Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene Mutation. Cerebellum (London, England) 16 (5-6) (2018)
Sándor Márki, Anikó Göblös, Eszter Szlávicz, Nóra Török, Péter Balicza, Benjamin Bereznai, Annamária Takáts, József Engelhardt, Klivényi Péter, László Vécsei, Mária Judit Molnár, Nikoletta Nagy, Márta Széll
The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population. Parkinson's disease 2018 (2018)