Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Martin Hložánek"'
Autor:
Pavel Kozner, Libor Eichenmann, Marie Ceska Burdova, Marketa Pavlikova, Martin Hlozanek, Dagmar Dotrelova
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Central retinal artery occlusion (CRAO) is an ophthalmologic emergency that can lead to irreversible loss of vision. Intravenous thrombolysis (IVT) has been used experimentally for its treatment. Our study aimed to evaluate the effect of eme
Externí odkaz:
https://doaj.org/article/7a6e24f9c49445ff9c899694be35fe36
Autor:
Lubica Dudakova, Pavlina Skalicka, Olga Ulmanová, Martin Hlozanek, Viktor Stranecky, Frantisek Malinka, Andrea L. Vincent, Petra Liskova
Publikováno v:
Journal of Ophthalmology, Vol 2020 (2020)
Background. The aim of the study was to identify the molecular genetic cause of two different Mendelian traits with ocular involvement present in the members of a single consanguineous Czech Roma family. Methods. We have performed ocular examination
Externí odkaz:
https://doaj.org/article/a9f5bf8ee86445b5839f539bb8755dd6
Autor:
Martin Hložánek, Zbyněk Straňák, Zuzana Terešková, Jan Mareš, Inka Krejčířová, Marie Česká Burdová
Publikováno v:
Diagnostics, Vol 12, Iss 5, p 1251 (2022)
Neonatal ophthalmic screening should lead to early diagnosis of ocular abnormalities to reduce long-term visual impairment in selected diseases. If a treatable pathology is diagnosed within a few days after the birth, adequate therapy may be indicate
Externí odkaz:
https://doaj.org/article/bbc3b5994e4341ae8fac26e645a13bce
Publikováno v:
Neurologie pro praxi. 24:88-93
Autor:
Marie Česká Burdová, Jana Štěpánková, Radka Kremlíková Pourová, Gabriela Mahelková, Martin Hložánek, Pavel Kožner, Dagmar Dotřelová
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 261:1723-1729
Autor:
Marie Česká, Burdová, Jana, Štěpánková, Radka Kremlíková, Pourová, Gabriela, Mahelková, Martin, Hložánek, Pavel, Kožner, Dagmar, Dotřelová
Publikováno v:
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie.
Stickler syndrome (STL) is an inherited progressive connective tissue collagen disorder. STL is the most common hereditary cause of retinal complications, retinal tears, and the development of retinal detachment (RD) in childhood. The aim of the stud
Autor:
Lenka Griščíková, Rudolf Autrata, Inka Krejčířová, Jorge L. Alió, Barbora Žajdlíková, Dana Tomčíková, Martin Hložánek
Publikováno v:
Journal of pediatric ophthalmology and strabismus.
Purpose: To evaluate the long-term efficacy of anterior chamber iris-fixated phakic intraocular lens (PIOL) implantation in the treatment of high myopic (> −9.00 diopters [D]) or hyperopic (> +6.00 D) anisometropia in children with intolerance to s
Publikováno v:
Czech and Slovak Ophthalmology. 77:28-34
Purpose: The aim of the study was to evaluate ocular surface and tear film in patients with pediatric (primary or secondary) unilateral glaucoma and compare results obtained from the treated eye and untreated healthy eye. Methods: Patients with unila
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b6b2265cef7acc97d69b08db8e1db1db
http://www.scopus.com/inward/record.url?eid=2-s2.0-33749151160&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33749151160&partnerID=MN8TOARS