Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Jabandziev, P."'
Autor:
Katerina Slaba, Petra Pokorna, Robin Jugas, Hana Palova, Dagmar Prochazkova, Stefania Aulicka, Klara Spanelova, Pavlina Danhofer, Ondrej Horak, Jana Tuckova, Petra Kleiblova, Renata Gaillyova, Matej Hrunka, Martin Jouza, Blanka Pinkova, Jan Papez, Petra Konecna, Jana Zidkova, Petr Stourac, Jaroslav Sterba, Regina Demlova, Eva Demlova, Petr Jabandziev, Ondrej Slaby
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract In the last decade, undiagnosed disease programs have emerged to address the significant number of individuals with suspected but undiagnosed rare genetic diseases. In our single-center study, we have launched a pilot program for pediatric p
Externí odkaz:
https://doaj.org/article/5632c7178ab1493c9496854f9b2ecf9d
Autor:
Jabandziev Petr, Hubacek Jaroslav Alois, Michalek Jaroslav, Jouza Martin, Papez Jan, Pecl Jakub, Slaba Katerina, Slaby Ondrej, Urik Milan, Aulicka Stefania, Kunovsky Lumir, Dominik Petr, Kratochvil Milan, Klucka Jozef, Stourac Petr
Publikováno v:
Romanian Journal of Internal Medicine, Vol 62, Iss 3, Pp 279-285 (2024)
Sepsis is one of the most common causes of death in patients admitted to intensive care units (ICUs). The development of sepsis is significantly influenced by genetic predisposition. In this study, we highlight a potential association between a varia
Externí odkaz:
https://doaj.org/article/b7b44aafc8854c1b9690e272645d972f
Publikováno v:
Maternal Health, Neonatology and Perinatology, Vol 10, Iss 1, Pp 1-6 (2024)
Abstract Background Imperforate hymen is the most common congenital defect of the female urogenital tract. The spectrum of clinical manifestations is broad, ranging from mild cases undiagnosed until adolescence to severe cases of giant intraabdominal
Externí odkaz:
https://doaj.org/article/86c5080e27ea40a2b6aa5ed26ecbea42
Autor:
Tamara Skrisovska, Jana Djakow, Petr Jabandziev, Tereza Kramplova, Jozef Klucka, Martina Kosinova, Petr Stourac
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionThis simulation-based study aimed to evaluate the efficacy of ventilation during paediatric cardiopulmonary resuscitation (CPR) provided by healthcare professionals (HCPs) and lay rescuers (LRs). The objective was to assess the number of
Externí odkaz:
https://doaj.org/article/e7d7d1b8a93d4feba2cba5112b67bc87
Autor:
Martin Sterba, Petra Pokorna, Renata Faberova, Blanka Pinkova, Jarmila Skotakova, Anna Seehofnerova, Jan Blatny, Lucia Janigova, Olga Koskova, Hana Palova, Michal Mahdal, Lukas Pazourek, Petr Jabandziev, Ondrej Slaby, Peter Mudry, Jaroslav Sterba
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract This was a prospective cohort study of eighteen patients with large and debilitating vascular malformations with one or more major systemic complications. In all patients, we discovered activating alterations in either TEK or PIK3CA. Based o
Externí odkaz:
https://doaj.org/article/a577de5101bc4a5b9cfe353e1382fac2
Publikováno v:
BMJ Paediatrics Open, Vol 7, Iss 1 (2023)
Although necrotising enterocolitis (NEC) is a serious, life-threatening disease, improved neonatal care is increasing the number of survivors with NEC among extremely preterm neonates. Therapy is nevertheless mostly symptomatic and the mortality rate
Externí odkaz:
https://doaj.org/article/19afc9e5d2d5415e81adfaeb09412495
Publikováno v:
Biomedical Papers, Vol 166, Iss 4, Pp 353-358 (2022)
Although symptoms of pancreatic diseases such as pancreatitis, acute and chronic and, carcinoma of the pancreas are mainly gastrointestinal in nature, the extra-pancreatic symptoms are also important. These include skin symptoms, such as pancreatic p
Externí odkaz:
https://doaj.org/article/cef8045aa2d54a8aab4b4e2f0456be15
Autor:
Katerina Slaba, Marta Jezova, Petra Pokorna, Hana Palova, Jana Tuckova, Jan Papez, Dagmar Prochazkova, Petr Jabandziev, Ondrej Slaby
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract Background Cardiac‐urogenital syndrome [MIM # 618280] is a newly described very rare syndrome associated with pathogenic variants in the myelin regulatory factor (MYRF) gene that leads to loss of protein function. MYRF is a transcription f
Externí odkaz:
https://doaj.org/article/a422a0e9cbef414ea6792e125f3ab57f
Autor:
Jiri Dolina, Lumir Kunovsky, Radek Kroupa, Karel Stary, Petr Jabandziev, Tereza Nesporova, Karel Maca, Tomas Andrasina, Filip Marek, Zdenek Kala, Jitka Vaculova, David Said, Martina Zapletalova, Jan Lochman, Hana Palova Noskova, Ondrej Slaby, Lydie Izakovicova Holla, Petra Borilova Linhartova
Publikováno v:
Biomedical Papers, Vol 166, Iss 2, Pp 228-235 (2022)
Background. Acromegaly is a disorder associated with hypersecretion of growth hormone, most usually caused by a pituitary adenoma. Dysmotility of the gastrointestinal tract has been reported in acromegalic patients. Achalasia is a disorder characteri
Externí odkaz:
https://doaj.org/article/83a2668532f247c28216fb5c4f930c85
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