Zobrazeno 1 - 10
of 3 740
pro vyhledávání: '"P100 Latency"'
Autor:
Papadopoulou, Athina, Pfister, Armanda, Tsagkas, Charidimos, Gaetano, Laura, Sellathurai, Shaumiya, D'Souza, Marcus, Cerdá-Fuertes, Nuria, Gugleta, Konstantin, Descoteaux, Maxime, Chakravarty, Mallar M., Fuhr, Peter, Kappos, Ludwig, Granziera, Cristina, Magon, Stefano, Sprenger, Till, Hardmeier, Martin
Publikováno v:
In Clinical Neurophysiology May 2024 161:122-132
Autor:
Sulejmanpašić, Gorana1 gsulejmanpasic@gmail.com, Memić-Serdarević, Amra1, Zahiragić, Amra1, Šabanagić-HajrićZ, Selma2
Publikováno v:
Medical Journal / Medicinski Žurnal. Jan-Mar2023, Vol. 29 Issue 1, p28-34. 7p.
Autor:
Koçtekin, Belkıs1 bkoctekin@gmail.com, Yüksel, Burcu2, Durmaz, Doğan3, Çilli, Mert Abdullah2, Tekindal, Mustafa Agah4, Çoban, Deniz Turgut3
Publikováno v:
Turkish Journal of Neurology / Turk Noroloji Dergisi. Sep2022, Vol. 28 Issue 3, p169-175. 7p.
Autor:
Belkıs Koçtekin, Burcu Yüksel, Doğan Durmaz, Mert Abdullah Çilli, Mustafa Agah Tekindal, Deniz Turgut Çoban
Publikováno v:
Türk Nöroloji Dergisi, Vol 28, Iss 3, Pp 169-175 (2022)
Objective: It was aimed to investigate the relationship of stereoacuity with retinal nerve fiber layer thickness (RNFLT) and P100 latency in multiple sclerosis (MS) patients with and without optic neuritis (ON). Materials and Methods: Twenty-nine pat
Externí odkaz:
https://doaj.org/article/958a02e9097d418b87148b55a8a47d90
Akademický článek
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Publikováno v:
International journal of health sciences. :3800-3810
Hypothyroidism is classified as congenital and acquired according to the time of onset. Consequences of thyroid gland dysfunction also depend on the life stage at which they occur. Peripheral and central nervous system dysfunction are important clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0f4bc02d73cab927e60632e2599347b
https://doi.org/10.53730/ijhs.v6ns3.6611
https://doi.org/10.53730/ijhs.v6ns3.6611
Autor:
Jasna Jancic, Nikola Zarkovic, Blazo Nikolic, Nikola Ivancevic, Branislav Rovcanin, Dejan Nesic
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionNeurofibromatosis type 1 (NF type 1) is an autosomal dominant disease with typical clinical manifestations, such as skin lesions, Lisch nodules, optic pathway gliomas, and neurofibromas, caused by the mutation of the NF1 gene. Visual evok
Externí odkaz:
https://doaj.org/article/4f471dc8701243298c092f4dcbfcfbf0
Kniha
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Autor:
Vecchio, Domizia1,2 (AUTHOR) domizia.vecchio@gmail.com, Barbero, Paolo1 (AUTHOR), Galli, Giulia1 (AUTHOR), Virgilio, Eleonora1,3 (AUTHOR), Naldi, Paola1 (AUTHOR), Comi, Cristoforo1,2 (AUTHOR), Cantello, Roberto1,2 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. Mar2023, Vol. 12 Issue 6, p2382. 7p.
Publikováno v:
Acta Informatica Medica. 30:318
Background: The VEPs provide an objective measure of brain function, analyzing integrity of visual processing. With patients affected with schizophrenia, the changes with the implementation of VEP are evident, such as symmetrical deceleration of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d3ce40540c187d1ccea0dde31f07e59
https://doi.org/10.5455/aim.2022.30.318-323
https://doi.org/10.5455/aim.2022.30.318-323