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Ideggyogyaszati Szemle|June 25, 2020
[The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]Mária Judit Molnár, Beáta Borsos, Katalin Visy Várdi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 28, 2020
Efficacy of nusinersen in type 1, 2 and 3 spinal muscular atrophy: Real world data from Hungarian patientsLéna Szabó, Anita Gergely, Rita Jakus, et al.
Frontiers in Medicine|May 13, 2026
Cognitive impairment, depression, and anxiety in systemic sclerosisVera Szekanecz, Laura Lekli, Lilla Bokor, et al.
American Journal of Physiology. Heart and Circulatory Physiology|April 10, 2016
Differences in the molecular structure of the blood-brain barrier in the cerebral cortex and white matter: an in silico, in vitro, and ex vivo studyÁdám Nyúl-Tóth, Maria Suciu, Judit Molnár, et al.
Journal of Biomolecular Screening|December 4, 2012
The use of microdialysis techniques in mice to study P-gp function at the blood-brain barrierIstván Sziráki, Franciska Erdő, Péter Trampus, et al.
Orvosi Hetilap|May 20, 2014
[Laboratory diagnosis of a rare congenital neurodegenerative disease: cerebrotendinous xanthomatosis]Viktória Evelin Varga, Mónika Katkó, János Harangi, et al.
Archives of Medical Science : AMS|September 15, 2021
Positive association and future perspectives of mitochondrial DNA copy number and telomere length - a pilot twin studyDóra Melicher, Anett Illés, Levente Littvay, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|August 11, 2018
Analysis of GJB2 mutations and the clinical manifestation in a large Hungarian cohortNóra Kecskeméti, Magdolna Szönyi, Anita Gáborján, et al.
Molecular Medicine (Cambridge, Mass.)|April 16, 2026
Genetic epidemiology of C9orf72 repeat expansion associated amyotrophic lateral sclerosis in HungaryZsófia Flóra Nagy, Adrienn Géresi, Zoltán Grosz, et al.
Orphanet Journal of Rare Diseases|October 16, 2020
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvementRoland Stengl, András Bors, Bence Ágg, et al.
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