Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Petr Jabandziev"'
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
Autor:
Jan Papez, Jiri Starha, Katerina Slaba, Jaroslav A Hubacek, Jakub Pecl, Stefania Aulicka, Milan Urik, Serdar Ceylaner, Petra Vesela, Ondrej Slaby, Petr Jabandziev
Publikováno v:
Biomedical Papers, Vol 165, Iss 4, Pp 454-457 (2021)
Background. Primary hypomagnesemia with secondary hypocalcemia (HSH) is a rare genetic disorder. Dysfunctional transient receptor potential melastatin 6 causes impaired intestinal absorption of magnesium, leading to low serum levels accompanied by hy
Externí odkaz:
https://doaj.org/article/41128d7da2d14bd8b8c01741231cabd0
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Sepsis is a major cause of lethality in neonatal intensive care units. Despite significant advances in neonatal care and growing scientific knowledge about the disease, 4 of every 10 infants born in developed countries and suffering from sepsis die o
Externí odkaz:
https://doaj.org/article/2eefee6048704011ace2e9f2b17e16d5
Autor:
Karolina Poredska, Lumir Kunovsky, Vladimir Prochazka, Jiri Dolina, Miroslava Chovancova, Jakub Vlazny, Tomas Andrasina, Michal Eid, Petr Jabandziev, Petr Kysela, Zdenek Kala
Publikováno v:
Diagnostic Pathology, Vol 14, Iss 1, Pp 1-4 (2019)
Abstract Background Neurofibromatosis type-1 (NF1), also called von Recklinghausen disease, is a rare genetic disease which can lead to the development of benign or even malignant tumors. NF1 is mostly diagnosed in children or early adolescents who p
Externí odkaz:
https://doaj.org/article/9d38fc24c703493bb6d5d833cd8090d0