Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Gordana Milosevski-Lomic"'
Autor:
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, Bahriye Atmis, Anja Büscher, Ute Derichs, Ismail Dursun, Ali Duzova, Loai Akram Eid, Matthias Galiano, Michaela Gessner, Ibrahim Gokce, Karsten Haeffner, Nakysa Hooman, Augustina Jankauskiene, Friederike Körber, Germana Longo, Laura Massella, Djalila Mekahli, Gordana Miloševski-Lomić, Hulya Nalcacioglu, Rina Rus, Rukshana Shroff, Stella Stabouli, Lutz T. Weber, Simone Wygoda, Alev Yilmaz, Katarzyna Zachwieja, Ilona Zagozdzon, Jörg Dötsch, Franz Schaefer, Max Christoph Liebau, The ARegPKD Consortium
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Autosomal recessive polycystic kidney disease (ARPKD) is characterized by bilateral fibrocystic changes resulting in pronounced kidney enlargement. Impairment of kidney function is highly variable and widely available prognostic markers are
Externí odkaz:
https://doaj.org/article/6626eaeb179242108171c93a0a824388
Autor:
Maria Bartosova, Betti Schaefer, Karel Vondrak, Peter Sallay, Christina Taylan, Rimante Cerkauskiene, Maria Dzierzega, Gordana Milosevski-Lomic, Rainer Büscher, Ariane Zaloszyc, Philipp Romero, Felix Lasitschka, Bradley A. Warady, Franz Schaefer, Akos Ujszaszi, Claus Peter Schmitt
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
The impact of peritoneal dialysis (PD) associated peritonitis on peritoneal membrane integrity is incompletely understood. Children are particularly suited to address this question, since they are largely devoid of preexisting tissue damage and life-
Externí odkaz:
https://doaj.org/article/4ae21a79027f45f290111fc263a669cd
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 146, Iss 1-2, Pp 77-80 (2018)
Introduction. Recently, inactivation mutations of CYP24A1, the gene encoding vitamin D 24-hydroxylase, were identified in hypercalciuric nephrolithiasis and nephrocalcinosis. Here, we describe а long-term follow-up of a patient with hypercalciuric n
Autor:
Mirjana Kostic, Amira Peco-Antic, Brankica Spasojevic, Mirjana Cvetkovic, Divna Kruscic, Gordana Milosevski-Lomic, Dusan Paripovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 3-4, Pp 147-152 (2017)
Introduction/Objective. Jeune syndrome (JS) is a rare hereditary ciliopathy characterized by asphyxiating thoracic dystrophy, shortened limbs and brachydactyly. Extraskeletal anomalies such as chronic renal failure (CRF), hepatic fibrosis, and retini
Autor:
Gordana Milosevski-Lomic, Amira Peco-Antic, Aleksandra Vukašinović, Tamara Ilisic, Jelena Kotur-Stevuljevic, Dusan Paripovic
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation
Oxidative stress seems to be an important link between obesity and cardiovascular disease. The aim of our study was to assess oxidative stress in obese patients stratified according to ambulatory blood pressure status and to determine independent pre
Autor:
Rosalie B Sterenborg, Jörg Dötsch, Bert Bammens, Samuel Kilian, Elke Wühl, Sarah Verbeeck, Djalila Mekahli, Rukshana Shroff, Günter Klaus, Kathrin Burgmaier, Gordana Milosevski-Lomic, Katja Sauerstein, Thomas Benzing, Laurence Michel-Calemard, Dorota Wicher, Franziska Grundmann, Bruno Ranchin, Lutz T. Weber, Franz Schaefer, Heiko Billing, Susanne Schaefer, Anja Büscher, Matthias Galiano, Max C. Liebau
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
Autosomal recessive polycystic kidney disease (ARPKD) is a severe pediatric hepatorenal disorder with pronounced phenotypic variability. A substantial number of patients with early diagnosis reaches adulthood and some patients are not diagnosed until
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9826ce8055f43f4939ae18b846046e
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85067279105
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85067279105
Autor:
Jelena Joksic, Aleksandra Zeljkovic, Jelena Janac, Jelena Vekic, Amira Peco-Antic, Dusan Paripovic, Osama H. Bekhet, Vesna Spasojevic-Kalimanovska, Zorana Jelic-Ivanovic, Gordana Milosevski-Lomic, Tamara Gojkovic
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation
Background: Obesity-related childhood hypertension is associated with disturbances of serum lipids, but less is known about distribution of lipoprotein subclasses and activities of proteins involved in reverse cholesterol transport in hypertensive ob
Autor:
Gordana Milosevski-Lomic, Natasa Stajic, Radovan Bogdanovic, Amira Peco-Antic, Milan Đukić, Dusan Paripovic, Zoran Krstic
Publikováno v:
Acta Paediatrica. 105:e35-e41
Aim This studied reviewed renovascular hypertension (RVH) due to renal artery stenosis (RAS) in two Serbian paediatric centres from 2001 to 2013. Methods The patients' demographic data, underlying syndromes, blood pressure (BP), antihypertensive trea
Autor:
Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta, Carsten Bergmann, Anja Katrin Buescher, Mathias Burgmaier, Ismail Dursun, Ali Duzova, Loai Eid, Florian Erger, Markus Feldkoetter, Matthias Galiano, Michaela Geßner, Heike Goebel, Ibrahim Gokce, Dieter Haffner, Nakysa Hooman, Bernd Hoppe, Augustina Jankauskiene, Guenter Klaus, Jens König, Mieczyslaw Litwin, Laura Massella, Djalila Mekahli, Engin Melek, Sevgi Mir, Lars Pape, Larisa Prikhodina, Bruno Ranchin, Raphael Schild, Tomas Seeman, Lale Sever, Rukshana Shroff, Neveen A. Soliman, Stella Stabouli, Malgorzata Stanczyk, Yilmaz Tabel, Katarzyna Taranta-Janusz, Sara Testa, Julia Thumfart, Rezan Topaloglu, Lutz Thorsten Weber, Dorota Wicher, Elke Wühl, Simone Wygoda, Alev Yilmaz, Katarzyna Zachwieja, Ilona Zagozdzon, Klaus Zerres, Jörg Dötsch, Franz Schaefer, Max Christoph Liebau, Nadejda Ranguelov, Nathalie Godefroid, Laure Collard, Jacques Lombet, Julie Maquet, Gesa Schalk, Uwe Querfeld, Bodo B. Beck, Thomas Benzing, Reinhard Buettner, Franziska Grundmann, Christine Kurschat, Kerstin Benz, Anja Tzschoppe, Björn Buchholz, Rainer Buescher, Karsten Häffner, Martin Pohl, Oliver Gross, Jenny Krügel, Johanna Stock, Ludwig Patzer, Jun Oh, Wanja Bernhardt, Anke Doyon, Tobias Vinke, Anja Sander, Michael Henn, Ute Derichs, Rolf Beetz, Nikola Jeck, Bärbel Lange-Sperandio, Sabine Ponsel, Franziska Kusser, Barbara Uetz, Marcus Benz, Silke Schmidt, Christina Huppertz-Kessler, Birgitta Kranz, Andrea Titieni, Donald Wurm, Heinz E. Leichter, Martin Bald, Heiko Billing, Marwa M. Nabhan, Luis Enrique Lara, Fotios Papachristou, Francesco Emma, Rimante Cerkauskiene, Karolis Azukaitis, Anna Wasilewska, Irena Balasz-Chmielewska, Monika Miklaszewska, Marcin Tkaczyk, Przemyslaw Sikora, Marcin Zaniew, Ania Niemirska, Jolanta Antoniewicz, Justyna Lesiak, Alberto Caldas Afonso, Ana Teixeira, Gordana Milosevski-Lomic, Dusan Paripović, Amira Peco-Antic, Svetlana Papizh, Aysun Karabay Bayazit, Ali Anarat, Alper Soylu, Salih Kavukcu, Cengiz Candan, Salim Caliskan, Nur Canpolat, Sevinc Emre, Harika Alpay, Nurver Akinci, Secil Conkar, Hakan M. Poyrazoglu, Ruhan Dusunsel
OBJECTIVE: To identify prenatal, perinatal, and postnatal risk factors for dialysis within the first year of life in children with autosomal recessive polycystic kidney disease (ARPKD) as a basis for parental counseling after prenatal and perinatal d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f6cfde1e35902f2f1dd74b9ce09f4a8
https://hdl.handle.net/20.500.12605/19675
https://hdl.handle.net/20.500.12605/19675
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 143, Iss 3-4, Pp 219-225 (2015)
A normal development of lower urinary tract function control evolves from involuntary bladder empting (incontinence) during infancy to daytime urinary continence, and finally a successful day and night continence that is generally achieved by the 5th