The role of hybrid FDG-PET/MRI on decision-making in presurgical evaluation of drug-resistant epilepsy

Autor: Márton Tóth, Péter Barsi, Zoltán Tóth, Katalin Borbély, János Lückl, Miklós Emri, Imre Repa, József Janszky, Tamás Dóczi, Zsolt Horváth, Péter Halász, Vera Juhos, Csilla Gyimesi, Beáta Bóné, Diána Kuperczkó, Réka Horváth, Ferenc Nagy, Anna Kelemen, Zsófia Jordán, Ákos Újvári, Koichi Hagiwara, Jean Isnard, Endre Pál, Attila Fekésházy, Dániel Fabó, Zsolt Vajda

Publikováno v: BMC Neurology, Vol 21, Iss 1, Pp 1-20 (2021)

Abstract Background When MRI fails to detect a potentially epileptogenic lesion, the chance of a favorable outcome after epilepsy surgery becomes significantly lower (from 60 to 90% to 20–65%). Hybrid FDG-PET/MRI may provide additional information

Externí odkaz: https://doaj.org/article/0fb81caa3bfa4ea1bfa57bc6bbb33af2

Small Fiber Neuropathy: Clinicopathological Correlations

Autor: Endre Pál, Krisztina Fülöp, Péter Tóth, Gabriella Deli, Zoltán Pfund, József Janszky, Sámuel Komoly

Publikováno v: Behavioural Neurology, Vol 2020 (2020)

Small fiber neuropathy develops due to the selective damage of the thin fibers of peripheral nerves. Many common diseases can cause this condition, including diabetes, infections, autoimmune and endocrine disorders, but it can occur due to genetic al

Externí odkaz: https://doaj.org/article/d7d3a1f664864dc8bbcac08ae95c3b96

Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

Autor: Zsolt Bánfai, Kinga Hadzsiev, Endre Pál, Katalin Komlósi, Márton Melegh, László Balikó, Béla Melegh

Publikováno v: BMC Medical Genetics, Vol 18, Iss 1, Pp 1-7 (2017)

Abstract Background Defects of the slow myosin heavy chain isoform coding MYH7 gene primarily cause skeletal myopathies including Laing Distal Myopathy, Myosin Storage Myopathy and are also responsible for cardiomyopathies. Scapuloperoneal and limb-g

Externí odkaz: https://doaj.org/article/11c4ce87bacd49b19c38023687eb5643

Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey

Autor: Lynda El-Hassar, Ahmed Amara, Benoit Sanson, Oana Lacatus, Ahmed Amir Belhouchet, Madelon Kroneman, Kristl Claeys, Jean Philippe Plançon, Carmelo Rodolico, Guido Primiano, Francesca Trojsi, Massimiliano Filosto, Tiziana Enrica Mongini, Sara Bortolani, Mauro Monforte, Elena Carraro, Lorenzo Maggi, Federica Ricci, Vincenzo Silani, Daniele Orsucci, Alain Créange, Yann Péréon, Tanya Stojkovic, Nadine Anna Maria Elisabeth van der Beek, Antonio Toscano, Davide Pareyson, Shahram Attarian, Peter Y.K. Van den Bergh, Gauthier Remiche, Janneke G.J. Hoeijmakers, Umesh Badrising, Nicol C. Voermans, Angela M. Kaindl, Ulrike Schara-Schmidt, Benedikt Schoser, Elisabetta Gazzerro, Jana Haberlová, Stanislav Voháňka, Endre Pál, Maria Judit Molnar, Lea Leonardis, Ivailo L Tournev, Andrés Nascimento Osorio, Montse Olivé, Nuria Muelas, Jorge Alonso-Perez, Francesc Plá, Marianne de Visser, Gabriele Siciliano, Sabrina Sacconi

Publikováno v: Journal of Neuromuscular Diseases, 10, 2, pp. 173-184
Journal of neuromuscular diseases, 10(2), 173-184. IOS Press
Journal of neuromuscular diseases, 10(2), 173-184. I O S Press
Journal of Neuromuscular Diseases, 10, 173-184
Journal of Neuromuscular Diseases, 10(2), 173-184. IOS Press BV

BACKGROUND: Telemedicine (TM) contributes to bridge the gap between healthcare facilities and patients' homes with neuromuscular disease (NMD) because of mobility issues. However, its deployment is limited due to difficulties evaluating subtle neurol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bab9186b51dc90db45ba25d891036f79
https://pubmed.ncbi.nlm.nih.gov/36373291

Implantálható kardioverter-defibrillátor által sikeresen megszüntetett malignus kamrai ritmuszavar dystrophia myotonicában szenvedő betegben

Autor: Dávid Varga, Réka Faludi, Tamás Simor, Dorottya Debreceni, Emese Lovadi, Endre Pál, Fanni Molnár, Eszter Fődi, Péter Kupó, Dalma Tényi

Publikováno v: Orvosi Hetilap. 162:1856-1858

Összefoglaló. A dystrophia myotonica (DM) multiszisztémás, autoszomális domináns módon öröklődő, többségében felnőttkori izombetegség, melynek incidenciája 1 : 8000. A betegség kapcsán fellépő izomszöveti degeneráció a haránt

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0798db70a1107b57264ad28300906743
https://doi.org/10.1556/650.2021.32279