Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Zdenek Kabelka"'
Autor:
Petra, Dytrych, Petra, Krol, Michaela, Kotrova, Daniela, Kuzilkova, Petr, Hubacek, Ladislav, Krol, Rami, Katra, Ondrej, Hrusak, Zdenek, Kabelka, Pavla, Dolezalova, Tomas, Kalina, Eva, Fronkova
Publikováno v:
In Molecular Immunology May 2015 65(1):139-147
Autor:
Jiri, Borsky, Jana, Veleminska, Michal, Jurovčík, Jiri, Kozak, Dana, Hechtova, Miroslav, Tvrdek, Milos, Cerny, Zdenek, Kabelka, Jaroslav, Fajstavr, Jan, Janota, Jiri, Zach, Renata, Peterkova, Miroslav, Peterka
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology November 2012 76(11):1616-1626
Autor:
Petr Janoušek, Marcela Malíková, Radka Kremlikova Pourova, O. Bendová, Emanuela Leonardi, Alessandra Murgia, Michal Jurovčík, Dagmar Rašková, Marcela Dvoráková, Pavel Seeman, Zdenek Kabelka, Jaromír Astl
Publikováno v:
Annals of Human Genetics. 74:299-307
Summary Mutations in SLC26A4 cause Pendred syndrome (PS) – hearing loss with goitre – or DFNB4 – non-syndromic hearing loss (NSHL) with inner ear abnormalities such as Enlarged Vestibular Aqueduct (EVA) or Mondini Dysplasia (MD). We tested 303
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b7277332dc29e24b4152579691c8207
https://doi.org/10.1111/j.1469-1809.2010.00581.x
https://doi.org/10.1111/j.1469-1809.2010.00581.x
Autor:
O. Bendová, Dagmar Rašková, M Kubálková, Daniel Groh, Zdenek Kabelka, Pavel Seeman, Marcela Malíková, Eva Seemanova, I Sakmaryová
Publikováno v:
Clinical Genetics. 66:152-157
Mutations in the gene gap junction beta 2 (GJB2), the gene for the connexin 26, are the most common cause of pre-lingual deafness worldwide. The mutation 35delG within GJB2 is prevalent in Europe. To date, there are no data about GJB2 mutation spectr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6703d6fdae9d4a12875dc73ed56cdce8
https://doi.org/10.1111/j.1399-0004.2004.00283.x
https://doi.org/10.1111/j.1399-0004.2004.00283.x
Autor:
Zdenek Kabelka, Milena Markova
Publikováno v:
International Congress Series. 1254:451-454
We have used Mitomycin C while treating patients with difficult laryngeal stenosis, stenosis of the subglottic area, and also for patients suffering from choanal atresia. The stenosis was originally caused by posttraumatic, post-intubation, and conge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72360df2ec62d8f10d79a21f1097f39e
https://doi.org/10.1016/s0531-5131(03)01077-x
https://doi.org/10.1016/s0531-5131(03)01077-x
Publikováno v:
Physiological research. 62(3)
The most frequent hereditary hearing loss is caused by mutations in the GJB2 gene coding for the gap junction beta 2 protein Connexin 26 (Cx26). In contrast to many studies performed in patients with bi-allelic mutations, audiometric studies on heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba6effbb0191f2de6b85fccf0059299c
https://pubmed.ncbi.nlm.nih.gov/23489192
https://pubmed.ncbi.nlm.nih.gov/23489192
Autor:
Zdenek Kabelka, Daniel Groh
Publikováno v:
Otolaryngology–Head and Neck Surgery. 143
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::048e871a067b8270cd94e91b4174df1a
https://doi.org/10.1016/j.otohns.2010.06.532
https://doi.org/10.1016/j.otohns.2010.06.532
Autor:
Jara Nedvidkova, Jiri Bronsky, Hana Krásničanová, Marie Vesela, Martin Chada, Michal Hrdlicka, Jiri Nevoral, Jiri Koutek, Richard Prusa, Zdenek Kabelka, Jana Schmidtova, Richard Kellermayer
Publikováno v:
The International journal of eating disorders. 44(6)
Objective: Orexin A (OXA) is a hypothalamic neuropeptide involved in regulation of food intake and nutritional status. There are multiple disturbances of neuropeptide signaling described in girls with anorexia nervosa (AN), but OXA levels have not be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35c09278a88e3c4a36dd3310d1a35b65
https://pubmed.ncbi.nlm.nih.gov/21823139
https://pubmed.ncbi.nlm.nih.gov/21823139
Autor:
Radka, Pourová, Petr, Janousek, Michal, Jurovcík, Marcela, Dvoráková, Marcela, Malíková, Dagmar, Rasková, Olga, Bendová, Emanuela, Leonardi, Alessandra, Murgia, Zdenek, Kabelka, Jaromír, Astl, Pavel, Seeman
Mutations in SLC26A4 cause Pendred syndrome (PS) - hearing loss with goitre - or DFNB4 - non-syndromic hearing loss (NSHL) with inner ear abnormalities such as Enlarged Vestibular Aqueduct (EVA) or Mondini Dysplasia (MD). We tested 303 unrelated Czec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a4d416eb3235a38eaaa8ac6c2237d40f
http://hdl.handle.net/11577/2466005
http://hdl.handle.net/11577/2466005
Publikováno v:
International journal of pediatric otorhinolaryngology. 74(5)
Objective Studies describing wound infections after cochlear implantation are rare. Meticulous operative techniques and sufficient surgical skill can help to avoid severe postoperative complications. Minor complications such as seromas, superficial w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::179e263f605dcdf6a1bc7654ae5173b2
https://pubmed.ncbi.nlm.nih.gov/20394849
https://pubmed.ncbi.nlm.nih.gov/20394849