Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Pavlína Plevová"'
Publikováno v:
Medicina, Vol 53, Iss 1, Pp 1-10 (2017)
The most frequent cause of familial glomerular hematuria is thin basement membrane nephropathy (TBMN) caused by germline COL4A3 or COL4A4 gene mutations. Less frequent but important cause with respect to morbidity is Alport syndrome caused by germlin
Externí odkaz:
https://doaj.org/article/5e7e97d88cf94f8bb1a8d2907a85efac
Autor:
Martin Komarc, Silvie Hrubá, Pavel Seeman, Pavlína Plevová, Vladimír Koucký, Rudolf Černý, Jan Kluh, Dagmar Rašková, Zuzana Balatková, Jan Plzak, Zdeněk Čada, Veronika Bandúrová, Jan Jencik, Jana Laštůvková, Simona Poisson Marková, Dana Šafka Brožková
Publikováno v:
European Archives of Oto-Rhino-Laryngology. 276:3353-3358
Hearing loss is the most frequent sensory disorder and is genetically extremely heterogeneous. By far the most frequent cause of nonsyndromic autosomal recessive hearing loss (AR-NSHL) are biallelic pathogenic mutations in the GJB2 gene causing DFNB1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d73ee6e5dc7ab24f7584df32fecbc4af
https://doi.org/10.1007/s00405-019-05649-5
https://doi.org/10.1007/s00405-019-05649-5
Autor:
Pavlína Kušnierová, Leos Pleva, Jana Zapletalová, Lucie Faldynova, Pavlína Plevová, Šárka Hilscherová, Petra Kovářová, Michal Karpisek, Pavel Kukla
Publikováno v:
Cor et Vasa. 59:e235-e239
Cil: Cilem nasi studie bylo posoudit vliv jednonukleotidových polymorfismů APOE (e2-rs7412, e4-rs429358) na koncentraci apolipoproteinu E v plazmě u pacientů s prokazanou ischemickou chorobou srdecni.Metody: Soubor tvořilo 94 pacientů s ischemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::222ce6b4da8045a5b5c7e687f4ed027a
https://doi.org/10.1016/j.crvasa.2016.11.011
https://doi.org/10.1016/j.crvasa.2016.11.011
Autor:
Pavlína Plevová
Publikováno v:
Klinicka Onkologie. 32
Background It is estimated that 5-10% of colorectal cancers arise due to a known genetic syndrome. Individuals with these cancer syndromes are also at risk of extracolonic cancers. Polyposis and nonpolyposis hereditary syndromes are generally recogni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e997342e95cae275e466757b253097d1
https://doi.org/10.14735/amko2019s97
https://doi.org/10.14735/amko2019s97
Autor:
Hedvika Geržová, Pavlína Plevová
Publikováno v:
Klinicka Onkologie. 32
Background Ovarian tumors in childhood and adolescence are distinguished from those that arise in adulthood by their histological subtype. These tumors may arise as the first manifestation of a cancer predisposition syndrome. Correct diagnosis of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9c0cc07399de87ae78c84b2c46605e0
https://doi.org/10.14735/amko2019s79
https://doi.org/10.14735/amko2019s79
Publikováno v:
Medicina, Vol 53, Iss 1, Pp 1-10 (2017)
The most frequent cause of familial glomerular hematuria is thin basement membrane nephropathy (TBMN) caused by germline COL4A3 or COL4A4 gene mutations. Less frequent but important cause with respect to morbidity is Alport syndrome caused by germlin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d61ea5afd678d98b39979448382ff27
http://www.sciencedirect.com/science/article/pii/S1010660X17300022
http://www.sciencedirect.com/science/article/pii/S1010660X17300022
Autor:
Petra Tvrda, Petra Turska, Pavlína Plevová, Eva Mrázková, Barbara Kantorova, Jana Zapletalová, Martina Paprskarova
Publikováno v:
Medicina; Volume 54; Issue 2; Pages: 28
Medicina
Medicina
Background and Objective: Hearing loss is the most common sensory deficit in humans. The aim of this study was to clarify the genetic aetiology of nonsyndromic hearing loss in the Moravian-Silesian population of the Czech Republic. Patients and Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::227e6a04a27f3fbc6376fde2f86f86dc
Autor:
Jana Zapletalová, Pavlína Plevová, Leos Pleva, Pavlína Kušnierová, Pavel Kukla, Petra Kovarova, Lucie Faldynova, Michal Karpisek
Publikováno v:
Biomedical Papers, Vol 159, Iss 4, Pp 586-594 (2015)
Aims: We sought to identify biochemical predictors that indicate susceptibility to in-stent restenosis (ISR) after coronary artery bare-metal stenting. Methods: A total of 111 consecutive patients with post-percutaneous coronary intervention (PCI) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ef9394f3e8faf69580972bd628389db
https://doi.org/10.5507/bp.2015.037
https://doi.org/10.5507/bp.2015.037
Autor:
Zdenek Svagera, Frantisek Vsiansky, Pavlína Kušnierová, Kristian Safarcik, Pavlína Plevová, Leos Pleva
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 75:508-513
The present study aimed to verify the reference intervals of plasma matrix metalloproteinases (MMPs) 2, 3, and 9 and serum asymmetric dimethylarginine (ADMA) in a healthy population with an average age corresponding to that of patients with cardiovas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd5201cc68a62570d0a54b4813a535be
https://doi.org/10.3109/00365513.2015.1057760
https://doi.org/10.3109/00365513.2015.1057760
Autor:
Petra Tvrda, Pavlína Plevová, Petra Turska, Eva Mrázková, Martina Paprskarova, Rastislav Slavkovsky
Publikováno v:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 38(10)
This study aimed to clarify the molecular epidemiology of hearing loss by identifying the responsible genes in patients without GJB2 mutations.Prospective genetic study.Tertiary referral hospital.Fifty one patients with bilateral sensorineural hearin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5870c3fd9986f6adfc0b1c7ca6d4b874
https://pubmed.ncbi.nlm.nih.gov/28984810
https://pubmed.ncbi.nlm.nih.gov/28984810