Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Zuzana Hrubá"'
Autor:
Zuzana Hrubá, Adéla Kotzianová, Ondřej Židek, Marek Pokorný, Vladimír Velebný, Štěpán Vondrovic
Publikováno v:
Textile Research Journal. 92:717-729
Traditional filtration media composed of fibers with sizes on the micrometer scale have difficulty filtering particles a little smaller than 300 nm. Even though nanofibrous materials are able to capture these particles and can have excellent filtrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0899d329415a203a7b302d8e83805e97
https://doi.org/10.1177/00405175211044164
https://doi.org/10.1177/00405175211044164
(AB)USE ME: A Mixed Reality Performance Installation Exploring Use of the Body as a Mediating Object
Publikováno v:
Lecture Notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering ISBN: 9783030734251
ArtsIT
ArtsIT
Performance art has long been used as a means for challenging various social constructs, such as ethics and personhood, and sometimes in ways which from the outside can appear traumatic for the performer – perhaps the most famous example being Mari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32b068bee9bb8b131f7358b92afe63bc
https://doi.org/10.1007/978-3-030-73426-8_4
https://doi.org/10.1007/978-3-030-73426-8_4
Publikováno v:
Minerva pediatrica.
Background Normalising growth in children with congenital adrenal hyperplasia due to 21- hydroxylase deficiency (21OHD-CAH) requires a long-term maintenance of a fragile balance between hydrocortisone (HC) replacement and androgen suppression. The gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a698abc6faa849dc362eb16c8512927b
https://pubmed.ncbi.nlm.nih.gov/32508077
https://pubmed.ncbi.nlm.nih.gov/32508077
Autor:
Kamila, Réblová, Zuzana, Hrubá, Dagmar, Procházková, Renata, Pazdírková, Slávka, Pouchlá, Jiří, Zeman, Lenka, Fajkusová
Publikováno v:
Clinica Chimica Acta
ICT FP7 Publications Database
OpenAIRE
ICT FP7 Publications Database
OpenAIRE
Background Hyperphenylalaninemia (HPA) is one of the most common inherited metabolic disorders caused by deficiency of the enzyme phenylalanine hydroxylase (PAH). HPA is associated with mutations in the PAH gene, which leads to reduced protein stabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab9a7e89becefa1562f183965099f6e
Autor:
Eva Sťahlová Hrabincová, Lenka Fajkusová, Zuzana Vrzalová, Felix Votava, Stanislava Kolouskova, Slávka Vrábelová, Zuzana Hrubá
Publikováno v:
European Journal of Medical Genetics. 54:112-117
Congenital adrenal hyperplasia (CAH) comprises a group of autosomal recessive disorders caused by an enzymatic deficiency which impairs the biosynthesis of cortisol and, in the majority of severe cases, also the biosynthesis of aldosterone. Approxima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20fed56bac19a5d4f7fdef9ae65f6697
https://doi.org/10.1016/j.ejmg.2010.10.005
https://doi.org/10.1016/j.ejmg.2010.10.005
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Wolfram-like syndrome (WFSL) is a rare autosomal dominant disease characterised by congenital progressive hearing loss, diabetes mellitus, and optic atrophy. The patient was a boy with the juvenile form of diabetes mellitus and findings which clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e3f6f174049ab1f46fe41e014d08c1
http://europepmc.org/articles/PMC5198010
http://europepmc.org/articles/PMC5198010
Autor:
Josef Zamecnik, Tat’ána Maříková, Jana Sedláčková, Lenka Fajkusová, Petr Vondráček, Markéta Hermanová, Josef Kraus, Zuzana Hrubá, Petra Hedvicakova, Jana Haberlová, Stanislav Voháňka
Publikováno v:
Neuromuscular Disorders. 19:749-753
Duchenne and Becker muscular dystrophies (DMD/BMD) are associated with mutations in the DMD gene. We determined the mutation status of 47 patients with dystrophinopathy without deletion or duplication in the DMD gene by screening performed by reverse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec19514ec9a9ba8caca0e19e920387b0
https://doi.org/10.1016/j.nmd.2009.08.011
https://doi.org/10.1016/j.nmd.2009.08.011
Autor:
Stanislava Kolouskova, Felix Votava, Lenka Fajkusová, Eva Hrabincová, Slávka Pouchlá, Zuzana Vrzalová, Zuzana Hrubá
Publikováno v:
International Journal of Molecular Medicine. 26
Congenital adrenal hyperplasia (CAH) is comprised of a group of autosomal recessive disorders caused by an enzymatic deficiency which impairs the biosynthesis of cortisol and, in most of the severe cases, also the biosynthesis of aldosterone. Approxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e08e7101bbc1edc1b4d1bfa4b848e5
https://doi.org/10.3892/ijmm_00000504
https://doi.org/10.3892/ijmm_00000504
Publikováno v:
Neuromuscular Disorders. 24:883
Limb-girdle muscular dystrophy (LGMD) is defined as a muscular dystrophy with predominantly proximal distribution of muscle weakness. It includes a number of disorders with heterogeneous etiology. We determined the frequency of recessive LGMD subtype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b364a34e87f475431af181d2be5506e8
https://doi.org/10.1016/j.nmd.2014.06.298
https://doi.org/10.1016/j.nmd.2014.06.298
Autor:
Kamila Réblová, Jiří Zeman, Slávka Pouchlá, Lenka Fajkusová, Dagmar Procházková, Renata Pazdírková, Zuzana Hrubá
Publikováno v:
Clinica Chimica Acta. 426:157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf26028c152b602fe00a3388a1ebda7b
https://doi.org/10.1016/j.cca.2013.10.010
https://doi.org/10.1016/j.cca.2013.10.010