Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renata, Pomahacova"'
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:
Alzbeta Santova, Lukas Plachy, Vit Neuman, Marketa Pavlikova, Lenka Petruzelkova, Petra Konecna, Petra Venhacova, Jaroslav Skvor, Renata Pomahacova, David Neumann, Jan Vosahlo, Jiri Strnadel, Kamila Kocourkova, Barbora Obermannova, Stepanka Pruhova, Ondrej Cinek, Zdenek Sumnik
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveTo compare parameters of glycemic control among three types of hybrid closed loop (HCL) systems in children with T1D (CwD) using population-wide data from the national pediatric diabetes registry ČENDA.MethodsCwD aged 12 months and monitore
Externí odkaz:
https://doaj.org/article/0779972e570f41b9a410c14b0e73f777
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
Autor:
Zdenek Sumnik, Marketa Pavlikova, Vit Neuman, Lenka Petruzelkova, Petra Konecna, Petra Venhacova, Jaroslav Skvor, Renata Pomahacova, David Neumann, Jan Vosahlo, Jiri Strnadel, Kamila Kocourková, Barbora Obermannova, Alzbeta Santova, Lukas Plachy, Stepanka Pruhova, Ondrej Cinek
Publikováno v:
Hormone Research in Paediatrics.
AIMS To assess the differences in key parameters of type 1 diabetes (T1D) control associated with treatment and monitoring modalities including newly introduced hybrid closed-loop (HCL) algorithm in children and adolescents with T1D (CwD) using the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f7c5a161217ee174b99359a868e687c
https://doi.org/10.1159/000530833
https://doi.org/10.1159/000530833
Publikováno v:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.
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 sex distrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e22754bcb6b790055cc1b0e3bd13d0b6
https://pubmed.ncbi.nlm.nih.gov/36504094
https://pubmed.ncbi.nlm.nih.gov/36504094
Autor:
Renata, Pomahacova, Petra, Paterova, Eva, Nykodymova, Eliska, Vaclavikova, Pavla, Sykorova, Katerina, Personova, Ramir, Katra, Ivan, Subrt, Josef, Sykora
Publikováno v:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia. 166(1)
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 medullary thyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffb7c4422858ebc7f94ff56ca947c1c5
https://pubmed.ncbi.nlm.nih.gov/34446941
https://pubmed.ncbi.nlm.nih.gov/34446941
Autor:
Renata, Pomahacova, Jana, Zamboryova, Petra, Paterova, Anna, Krepelova, Ivan, Subrt, Radka, Jaklova, Petra, Vohradska, Eliska, Hrdonkova, Josef, Sykora
Publikováno v:
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia. 163(4)
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 X. These chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b6a6d80d6c40b57b6ea9838ba40b1f1
https://pubmed.ncbi.nlm.nih.gov/30401990
https://pubmed.ncbi.nlm.nih.gov/30401990