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1دورية أكاديمية
المؤلفون: Nicole Anteneová, Silvie Kelifová, Hana Kolářová, Alžběta Vondráčková, Iveta Tóthová, Petra Lišková, Martin Magner, Josef Zámečník, Hana Hansíková, Jiří Zeman, Markéta Tesařová, Tomáš Honzík
المصدر: Brain Sciences, Vol 10, Iss 11, p 766 (2020)
مصطلحات موضوعية: Kearns-Sayre Syndrome (KSS) Spectrum, Progressive External Ophthalmoplegia (PEO), Pearson Syndrome, mtDNA, Single, Large-Scale Mitochondrial DNA Deletions (SLSMD), Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Iveta Tóthová, Dušan Igaz, Jaroslav Antal
المصدر: Journal of Environmental Engineering and Landscape Management, Vol 15, Iss 2 (2007)
مصطلحات موضوعية: soil, water content, moisture, mathematical Global Model, correlation, gravimetric method, Environmental engineering, TA170-171
وصف الملف: electronic resource
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المؤلفون: Sarah L. Stenton, Marketa Tesarova, Natalia L. Sheremet, Claudia B. Catarino, Valerio Carelli, Elżbieta Ciara, Kathryn Curry, Martin Engvall, Leah R. Fleming, Peter Freisinger, Katarzyna Iwanicka-Pronicka, Elżbieta Jurkiewicz, Thomas Klopstock, Mary K. Koenig, Hana Kolářová, Bohdan Kousal, Tatiana Krylova, Chiara La Morgia, Lenka Nosková, Dorota Piekutowska-Abramczuk, Sam N. Russo, Viktor Stránecký, Iveta Tóthová, Frank Träisk, Holger Prokisch
المصدر: Brain 145, 1624-1631 (2022)
Brain 145(5), 1624-1631 (2022). doi:10.1093/brain/awac052مصطلحات موضوعية: Adult, Male, genetic structures, genetics [Mutation], Optic Atrophy, Hereditary, Leber, Dnajc30, Lhon, Leigh Syndrome, Mitochondrial Disease, genetics [DNA, Mitochondrial], Leigh syndrome, DNA, Mitochondrial, DNAJC30, eye diseases, LHON, mitochondrial disease, genetics [Optic Atrophy, Hereditary, Leber], Optic Atrophies, Hereditary, Mutation, genetics [Leigh Disease], Humans, Female, ddc:610, Neurology (clinical), Leigh Disease, Child
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2bf87daded9ca23e3b2756c60479a76
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=64376 -
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المؤلفون: Dana Gabriková, Martin Mistrík, Jarmila Bernasovská, Iveta Tóthová, Jana Kisková
مصطلحات موضوعية: HK1, HSMN-Russe, rare disease, Gypsies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b99bea70744a6915dcccb2b5fb5298fc
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5
المؤلفون: Niklas Dahl, Doroteya Raykova, Iveta Tóthová, Joakim Klar, Alkwin Wanders, Elisabet Gustafson, Adam Ameur
المصدر: European journal of human genetics : EJHG. 23(12)
مصطلحات موضوعية: Adult, Male, Pathology, medicine.medical_specialty, Adolescent, Duodenum, Urinary system, Molecular Sequence Data, Urinary Bladder, Uterus, Mutation, Missense, Biology, Article, Genetics, medicine, Missense mutation, Humans, Amino Acid Sequence, Child, Genetics (clinical), Actin, Intestinal Pseudo-Obstruction, Middle Aged, Phenotype, Small intestine, Actins, Pedigree, medicine.anatomical_structure, Biliary tract, Female, Hypoperistalsis