Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Tomas Seeman"'
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:
Djalila Mekahli, Max C. Liebau, Melissa A. Cadnapaphornchai, Stuart L. Goldstein, Larry A. Greenbaum, Mieczyslaw Litwin, Tomas Seeman, Franz Schaefer, Lisa M. Guay-Woodford
Publikováno v:
BMC Nephrology, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Purpose Autosomal recessive polycystic kidney disease (ARPKD) is a hereditary condition characterized by massive kidney enlargement and developmental liver defects. Potential consequences during childhood include the need for kidney replacem
Externí odkaz:
https://doaj.org/article/1bf40945d1034d07a5ca7a9914231cc8
Autor:
Elke Wühl, Javier Calpe, Dorota Drożdż, Serap Erdine, Fernando Fernandez-Aranda, Adamos Hadjipanayis, Peter F. Hoyer, Augustina Jankauskiene, Susana Jiménez-Murcia, Mieczysław Litwin, Giuseppe Mancia, Artur Mazur, Denes Pall, Tomas Seeman, Manish D. Sinha, Giacomo Simonetti, Stella Stabouli, Empar Lurbe
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
The joint statement is a synergistic action between HyperChildNET and the European Academy of Pediatrics about the diagnosis and management of hypertension in youth, based on the European Society of Hypertension Guidelines published in 2016 with the
Externí odkaz:
https://doaj.org/article/6b775198f59e431c8e00e341682db0a7
Autor:
Empar Lurbe, Giuseppe Mancia, Javier Calpe, Dorota Drożdż, Serap Erdine, Fernando Fernandez-Aranda, Adamos Hadjipanayis, Peter F. Hoyer, Augustina Jankauskiene, Susana Jiménez-Murcia, Mieczysław Litwin, Artur Mazur, Denes Pall, Tomas Seeman, Manish D. Sinha, Giacomo Simonetti, Stella Stabouli, Elke Wühl
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
The joint statement is a synergistic action between HyperChildNET and the European Academy of Pediatrics about the diagnosis and management of hypertension in youth, based on the European Society of Hypertension Guidelines published in 2016 with the
Externí odkaz:
https://doaj.org/article/74f908ee39814bddaca2539e8669a728
Autor:
Martin Bezdicka, Filip Kaufman, Ivana Krizova, Alzbeta Dostalkova, Michaela Rumlova, Tomas Seeman, Karel Vondrak, Filip Fencl, Jakub Zieg, Ondrej Soucek
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Approximately one third of children with steroid-resistant nephrotic syndrome (SRNS) carry pathogenic variants in one of the many associated genes. The WT1 gene coding for the WT1 transcription factor is among the most frequently affected ge
Externí odkaz:
https://doaj.org/article/b11a26d8ae524e0d88fce9c3e005a802
Autor:
Josep Redon, Tomas Seeman, Dénes Pall, Lagle Suurorg, Konstantinos Kamperis, Serap Erdine, Elke Wühl, Giuseppe Mancia
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
IntroductionTo date, our knowledge on antihypertensive pharmacological treatment in children and adolescents is still limited because there are few randomized clinical trials (CTs), hampering appropriate management. The objective was to perform a nar
Externí odkaz:
https://doaj.org/article/87dd8422b455415dbb388683e9b03bc8
Autor:
Richard Klaus, Annette Friederike Jansson, Matthias Griese, Tomas Seeman, Kerstin Amann, Bärbel Lange-Sperandio
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Pediatric sarcoidosis is a complex inflammatory disorder with multisystemic manifestations. Kidney involvement in children is rare, and prognostic factors are unknown.Case Report and Methods: We report the case of a 16-year-old girl with
Externí odkaz:
https://doaj.org/article/ce368b8224f04cadbbc9c77fd979c0b3
Autor:
Lena Obeidova, Tomas Seeman, Filip Fencl, Kveta Blahova, Jan Hojny, Veronika Elisakova, Jana Reiterova, Jitka Stekrova
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0235071 (2020)
Cystic kidney diseases are a very heterogeneous group of chronic kidney diseases. The diagnosis is usually based on clinical and ultrasound characteristics and the final diagnosis is often difficult to be made. Next-generation sequencing (NGS) may he
Externí odkaz:
https://doaj.org/article/40e5750d5d9e4ed0b7b184e68fb455e3
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Publikováno v:
Case Reports in Nephrology and Dialysis, Vol 14, Iss 1, Pp 104-109 (2024)
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, which is mainly caused by pathogenic variants in two particular genes: PKD1 and PKD2. ADPKD caused by variants in other genes (GANAB or I
Externí odkaz:
https://doaj.org/article/1e348d8228474ea885b6928b6d0fa88b