Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ludmila Podracká"'
Autor:
Leonardo Gatticchi, Jan Miertus, Paolo Enrico Maltese, Simone Bressan, Luca De Antoni, Ludmila Podracká, Lucia Piteková, Vanda Rísová, Mari Mällo, Kaie Jaakson, Kairit Joost, Leonardo Colombo, Matteo Bertelli
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background Alström syndrome is a rare recessively inherited disorder caused by variants in the ALMS1 gene. It is characterized by multiple organ dysfunction, including cone-rod retinal dystrophy, dilated cardiomyopathy, hearing loss, obesit
Externí odkaz:
https://doaj.org/article/430cf243a6be4a2283a903b579084f56
Autor:
Loes Oomen, Charlotte M. H. H. T. Bootsma-Robroeks, Antonia H. M. Bouts, Mar Carbonell Pradas, Romy Gander, Katrin Kienzl-Wagner, Paul König, Pedro Lopez Pereira, Olivier Dunand, Sara M. F. S. Mosca, Michal Pac, Ludmila Podracka, Agnieszka A. Prytula, Maria Sangermano, Renata Vitkevic, Jakub Zieg, Loes F. M. van der Zanden, Wout F. J. Feitz, Liesbeth L. de Wall
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundPediatric kidney transplantations are rarely performed, and there is limited knowledge about the diversity in current clinical practices across Europe. This study aims to explore the utility of clinical snapshot studies in identifying these
Externí odkaz:
https://doaj.org/article/5446d87be2d04f74a3041f048e52986b
Autor:
Simone Bressan, Leonardo Gatticchi, Paolo Enrico Maltese, Leonardo Colombo, Ludmila Podracká, Vanda Rísová, Luca De Antoni, Kaie Jaakson, Mari Mällo, Jan Miertus, Lucia Piteková, Matteo Bertelli, Kairit Joost
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Background Alström syndrome is a rare recessively inherited disorder caused by variants in the ALMS1 gene. It is characterized by multiple organ dysfunction, including cone-rod retinal dystrophy, dilated cardiomyopathy, hearing loss, obesity, insuli
Diversity of kidney care referral pathways in national child health systems of 48 European countries
Autor:
Velibor Tasic, Vidar O. Edvardsson, Evgenia Preka, Larisa Prikhodina, Constantinos J. Stefanidis, Rezan Topaloglu, Diamant Shtiza, Ashot Sarkissian, Thomas Mueller-Sacherer, Rena Fataliyeva, Ina Kazyra, Elena Levtchenko, Danka Pokrajac, Dimitar Roussinov, Danko Milošević, Avraam Elia, Tomas Seeman, Mia Faerch, Inga Vainumae, Janne Kataja, Michel Tsimaratos, Irakli Rtskhiladze, Peter F. Hoyer, George Reusz, Atif Awan, Danny Lotan, Licia Peruzzi, Nazim Nigmatullina, Nasira Beishebaeva, Edite Jeruma, Augustina Jankauskiene, Olivier Niel, Valerie Said-Conti, Angela Ciuntu, Snežana Pavićević, Michiel Oosterveld, Anna Bjerre, Marcin Tkaczyk, Ana Teixeira, Adrian C. Lungu, Alexey Tsygin, Vesna Stojanović, Ludmila Podracka, Tanja Kersnik Levart, Mar Espino-Hernández, Per Brandström, Giuseppina Sparta, Harika Alpay, Dmytro Ivanov, Jan Dudley, Komiljon Khamzaev, Dieter Haffner, Jochen Ehrich
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundPrimary, secondary and tertiary healthcare services in Europe create complex networks covering pediatric subspecialties, sociology, economics and politics. Two surveys of the European Society for Paediatric Nephrology (ESPN) in 1998 and 201
Externí odkaz:
https://doaj.org/article/f14fb7b985dd4342a50d5e772886dda3
Autor:
Kristina Podolakova, Lubomir Barak, Emilia Jancova, Simona Tarnokova, Ludmila Podracka, Zuzana Dobiasova, Martina Skopkova, Daniela Gasperikova, Juraj Stanik
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Little is known about complete remission in Type 1 diabetes mellitus (T1D) with the discontinuance of insulin treatment for a period of time. In this retrospective study we analysed the frequency and factors of onset and duration of 1. remis
Externí odkaz:
https://doaj.org/article/a1782293193f42c8add2061e0b80e967
Autor:
Alexandra Gaál Kovalčíková, Ľubica Janovičová, Július Hodosy, Janka Bábíčková, Diana Vavrincová-Yaghi, Peter Vavrinec, Peter Boor, Ľudmila Podracká, Katarína Šebeková, Peter Celec, Ľubomíra Tóthová
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Extracellular DNA (ecDNA) in plasma is a non-specific biomarker of tissue damage. Urinary ecDNA, especially of mitochondrial origin, is a potential non-invasive biomarker of kidney damage. Despite prominent tissue damage, ecDNA has not yet b
Externí odkaz:
https://doaj.org/article/cd8186a4d9ed4c5c8ccb87bd4b7f0108
Publikováno v:
Children, Vol 11, Iss 1, p 66 (2024)
The presence of metabolic syndrome (MetS) increases the risk of developing type 2 diabetes, cardiovascular diseases, and mortality. MetS is associated with increased leukocyte or erythrocyte counts. In 16- to 20-year-old males (n = 1188) and females
Externí odkaz:
https://doaj.org/article/2b8ace37c164459eb8060cabfc43c3ff
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background Obesity and hypertension represent serious health issues affecting the pediatric population with increasing prevalence. Hypovitaminosis D has been suggested to be associated with arterial hypertension. Serotonin by modulating nitr
Externí odkaz:
https://doaj.org/article/d806bcd9ce9249238c5cadf7f1653157
Autor:
Katarína Krivošíková, Nadja Šupčíková, Alexandra Gaál Kovalčíková, Jakub Janko, Michal Pastorek, Peter Celec, Ľudmila Podracká, Ľubomíra Tóthová
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundUrinary tract infections (UTI) are common types of bacterial infection in children. UTI treatment is aimed to prevent complications including hypertension, proteinuria, and progression to chronic kidney disease. Activated neutrophils releas
Externí odkaz:
https://doaj.org/article/59105dd0f7ce4eddb0b6dbdd98c67de5
Autor:
Johnson S, Stojanovic J, Ariceta G, Bitzan M, Besbas N, Frieling M, Karpman D, Landau D, Langman C, Licht C, Pecoraro C, Riedl M, Siomou E, van de Kar N Walle JV, Loirat C, Taylor CM, Anne-Laure Adra, Klaus Arbeiter, Yelda Bilginer, Heiko Billing, Maria Bitsori, Bernard Boudailliez, Francisco de la Cerda – Ojeda, Gérard Champion, Amit Dagan, Bradley Dixon, Philippe Eckart, Israel Eisenstein, Arnaud Garnier, Clara Gomes, Karsten Häffner, Jerome Harambat, Carol Inward, Rafael Krmar, Theresa Kwon, Anne-Laure Lapeyraque, Sebastian Loos, Meeta Malik, Mignon McCulloch, David Milford, Danko Milosevic, Carla Nester, François Nobili, Pedro J Ortega, Fotios Papachristou, Antonia Peña - Carrión, Ludmila Podracká, Nikoleta Printza, Bruno Ranchin, Christopher Reid, Caroline Rousset-Rouvière, Rémi Salomon, Anne-Laure Sellier-Leclerc, James Springate, Sophie Taque, Despoina Tramma, Sibylle Tschumi, Ulrike Walden, Kay Tyerman, Aoife Waters, Donald J Weaver Jr
Publikováno v:
Pediatric Nephrology, 29, 10, pp. 1967-78
Pediatric Nephrology, 29, 1967-78
Pediatric Nephrology, 29, 1967-78
Item does not contain fulltext BACKGROUND: In 2009, the European Paediatric Study Group for Haemolytic Uraemic Syndrome (HUS) published a clinical practice guideline for the investigation and initial therapy of diarrhea-negative HUS (now more widely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7cfc2ff06baa3cd6fd37ac75199a0be
https://hdl.handle.net/2066/138690
https://hdl.handle.net/2066/138690