Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Lukáš VARGA"'
Publikováno v:
Listy klinicke logopedie, Vol 8, Iss 1, Pp 11-17 (2024)
Unilateral laryngeal paresis can lead to dysphonia as well as respiratory and swallowing deficits. The pathomechanism of swallowing dysfunction in unilateral laryngeal paresis is decreased sensitivity of supraglottic structures, impaired protective f
Externí odkaz:
https://doaj.org/article/6722e90e79be42b28d59ae4afd50fb65
Autor:
Lukáš VARGA, Peter J. FEDOR
Publikováno v:
Plant Protection Science, Vol 44, Iss 4, Pp 155-159 (2008)
Echinothrips americanus Morgan, 1913, is one of the pest species that expanded their area of distribution in a relatively short time. Being native to the eastern parts of North America, its first European interception was recorded in 1989. Since then
Externí odkaz:
https://doaj.org/article/52eeb885310243d79da9fb14604d890d
Autor:
Lukáš Varga
Publikováno v:
Plant Protection Science, Vol 44, Iss 3, Pp 114-118 (2008)
Monitoring of pest species in plant production and extended trade on ornamental plant material, including precise identification, are the main goals of modern plant protection. As a result, a new species of phytophagous thrips - Hercinothrips femoral
Externí odkaz:
https://doaj.org/article/ae1f665d87444107a824f5f9ab9dc4b5
Autor:
Ivica Mašindová, Andrea Šoltýsová, Lukáš Varga, Petra Mátyás, Andrej Ficek, Miloslava Hučková, Martina Sůrová, Dana Šafka-Brožková, Saima Anwar, Judit Bene, Slavomír Straka, Ingrid Janicsek, Zubair M Ahmed, Pavel Seeman, Béla Melegh, Milan Profant, Iwar Klimeš, Saima Riazuddin, Ľudevít Kádasi, Daniela Gašperíková
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0124232 (2015)
In the present study we aimed: 1) To establish the prevalence and clinical impact of DFNB49 mutations in deaf Roma from 2 Central European countries (Slovakia and Hungary), and 2) to analyze a possible common origin of the c.1331+2T>C mutation among
Externí odkaz:
https://doaj.org/article/2211c17f1c124b1f8927900caae4f350
Autor:
Diana Ugorová, Zuzana Polakovičová, Irena Dobišová, Ľubica Pejhovská, Darina Chovancová, Milan Profant, Lukáš Varga
Publikováno v:
Otorinolaryngologie a foniatrie. 71:210-217
Congenital cytomegalovirus infection (cCMV) is the most common non-genetic cause of congenital sensorineural hearing loss (SNHL) and one of the most prevalent inborn infections. Its symptoms are variable, from thrombocytopenia to neurodevelopmental d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7bbb1e33470cbf37f410a61644aa294
https://doi.org/10.48095/ccorl2022210
https://doi.org/10.48095/ccorl2022210
Autor:
Pavel Doležal, E. Račeková, Marcela Martončíková, M. Skálová, Lukáš Varga, Miroslav Tedla, P. Lukášek, Vladimír Čalkovský, Rastislav Zigo, J. Večeřa, Š. Dobrovič, Tomáš Pniak, M. Sabo, M. Almaši, J. Korch, I. Hriseňko, S. Straka
Publikováno v:
Otorinolaryngologie a foniatrie. 71:147-155
Objective: The aim of this study is to fi nd out how many patients with an ongoing smell and taste disorder after COVID-19 infection, can improve the subjective perception of smell by olfactory training method. Methods: Patients after COVID-19 (fi rs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::569de03b6589fafa7b67afbe0234db53
https://doi.org/10.48095/ccorl2022147
https://doi.org/10.48095/ccorl2022147
Publikováno v:
Otorinolaryngologie a foniatrie. 71:24-32
Otitis media is one of the most common diseases in the world and generally it also belongs to the most frequent causes of hearing loss. In some cases, it may progress to chronic otitis media despite adequate initial treatment. Due to its complex path
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f10db6faa23bb2662025c56c13f9b37
https://doi.org/10.48095/ccorl202224
https://doi.org/10.48095/ccorl202224
Autor:
Dana Safka Brozkova, Anna Uhrova Meszarosova, Petra Lassuthova, Lukáš Varga, David Staněk, Silvia Borecká, Jana Laštůvková, Vlasta Čejnová, Dagmar Rašková, Filip Lhota, Daniela Gašperíková, Pavel Seeman
Publikováno v:
Genes
Volume 12
Issue 5
Genes, Vol 12, Iss 684, p 684 (2021)
Volume 12
Issue 5
Genes, Vol 12, Iss 684, p 684 (2021)
Hearing loss is a genetically heterogeneous sensory defect, and the frequent causes are biallelic pathogenic variants in the GJB2 gene. However, patients carrying only one heterozygous pathogenic (monoallelic) GJB2 variant represent a long-lasting di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::dfb625f49cb907360b7f77608b598457
http://europepmc.org/articles/PMC8147375
http://europepmc.org/articles/PMC8147375
Autor:
Zuzana Pavlenkova, Lukas Varga, Silvia Borecka, Miloslav Karhanek, Miloslava Huckova, Martina Skopkova, Milan Profant, Daniela Gasperikova
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract The genetic heterogeneity of sensorineural hearing loss (SNHL) is a major hurdle to the detection of disease-causing variants. We aimed to identify underlying causal genes associated with mid-frequency hearing loss (HL), which contributes to
Externí odkaz:
https://doaj.org/article/d07c4be76fda4d4d81919144ffb8c089
Autor:
Dana Safka Brozkova, Lukas Varga, Anna Uhrova Meszarosova, Zuzana Slobodova, Martina Skopkova, Andrea Soltysova, Andrej Ficek, Jan Jencik, Jana Lastuvkova, Daniela Gasperikova, Pavel Seeman
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background The Roma are a European ethnic minority threatened by several recessive diseases. Variants in MANBA cause a rare lysosomal storage disorder named beta-mannosidosis whose clinical manifestation includes deafness and mental retardat
Externí odkaz:
https://doaj.org/article/da7c7f77811c48b19db2cb2862fd08af