Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Petra Paterová"'
Autor:
Renata, Pomahačová (AUTHOR), Petra, Paterová (AUTHOR), Eva, Nykodýmová (AUTHOR), Petr, Polák (AUTHOR), Josef, Sýkora (AUTHOR)
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie. 2023 Supplement 3, Vol. 78, p17-21. 5p.
Autor:
Renata, Pomahačová (AUTHOR), Petra, Paterová (AUTHOR), Eva, Nykodýmová (AUTHOR), Eva, Sládková (AUTHOR), Eva, Skalická (AUTHOR), Josef, Sýkora (AUTHOR)
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie. 2022 Supplement 3, Vol. 77, p24-29. 6p.
Publikováno v:
Česko-slovenská pediatrie. 77:S24-S29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99e4af3c11cf8cf894559f4a765df2a4
https://doi.org/10.55095/cspediatrie2022/055
https://doi.org/10.55095/cspediatrie2022/055
Publikováno v:
Biomedical Papers, Vol 168, Iss 1, Pp 85-91 (2024)
Background. We report four pediatric subjects with Cushing's disease (CD) diagnosed in the Czech Republic. We focus on initial symptoms of Cushing's syndrome (CS) which can lead to early diagnosis, on typical symptoms of CS in children, their age and
Externí odkaz:
https://doaj.org/article/e009776022c14678ba1c82a76d4116f4
Autor:
Renata Pomahacova, Petra Paterova, Eva Nykodymova, Petr Polak, Eva Sladkova, Eva Skalicka, Josef Sykora
Publikováno v:
Biomedical Papers, Vol 167, Iss 4, Pp 328-334 (2023)
Obesity has become a serious medical condition where many factors can contribute to excess weight gain. The most common type of childhood obesity is simple obesity, which is due to gene-obesogenic environment interaction. Only a minority are due to p
Externí odkaz:
https://doaj.org/article/beabd39042cc4a4cb63e5f5cd3ddcea6
Autor:
Jiří Dort, Zdeňka Černá, Ivan Subrt, Jana Zamboryová, Václav Lád, Eva Dortová, Karel Fiklík, Josef Sýkora, Petr Jehlička, Petra Paterová, Renata Pomahačová, Tomas Votava
Publikováno v:
Pediatric Diabetes. 18:844-847
Thiamine-responsive megaloblastic anemia (TRMA) is a rare autosomal recessive disorder caused by mutations in the SLC19A2 gene. To date at least 43 mutations have been reported for the gene encoding a plasma membrane thiamine transporter protein (THT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aa740a49e33beaecc8bdc884f936666
https://doi.org/10.1111/pedi.12479
https://doi.org/10.1111/pedi.12479
Autor:
Renata Pomahacova, Petra Paterova, Eva Nykodymova, Eliska Vaclavikova, Pavla Sykorova, Katerina Personova, Ramir Katra, Ivan Subrt, Josef Sykora
Publikováno v:
Biomedical Papers, Vol 166, Iss 1, Pp 105-111 (2022)
Background. We describe early and typical nonendocrine symptoms of Multiple Endocrine Neoplasia type 2B (MEN2B) presented in our patients with de novo M918T mutation in the RET proto-oncogene in early childhood, however, the diagnosis of MEN2B and me
Externí odkaz:
https://doaj.org/article/662a3280e1ca4c23806c7841c615f859
Autor:
Renata Pomahacova, Jana Zamboryova, Petra Paterova, Anna Krepelova, Ivan Subrt, Radka Jaklova, Petra Vohradska, Eliska Hrdonkova, Josef Sykora
Publikováno v:
Biomedical Papers, Vol 163, Iss 4, Pp 379-382 (2019)
Background: The complete androgen insensitivity syndrome (CAIS) is a rare genetic disorder causing insensitivity to androgens in a person with female phenotype and 46,XY karyotype due to a mutation in the androgen receptor gene located on chromosome
Externí odkaz:
https://doaj.org/article/0332d4c50b394dc4aa42a5bae7d2cb0d
Autor:
Renata Pomahacova, Jana Zamboryova, Petra Paterova, Karel Fiklik, Zdenka Cerna, Vaclav Lad, Eva Skalicka, Michal Huml, Josef Sykora
Publikováno v:
Biomedical Papers, Vol 162, Iss 4, Pp 289-293 (2018)
Background: The prevalence of autoimmune thyroiditis (AIT), as the most common autoimmune disease (AD) and papillary thyroid cancer (PTC) is steadily rising in children. The aim of this study was to determine the coexistence of other AD and thyroid c
Externí odkaz:
https://doaj.org/article/0c634a3c30434bddb2a45a956cc52eaf