M
Monika Miklaszewska
Researcher at Jagiellonian University Medical College
Publications - 68
Citations - 834
Monika Miklaszewska is an academic researcher from Jagiellonian University Medical College. The author has contributed to research in topics: Kidney disease & Nephropathy. The author has an hindex of 13, co-authored 65 publications receiving 541 citations. Previous affiliations of Monika Miklaszewska include University of Szeged & Boston Children's Hospital.
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Journal ArticleDOI
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
Miguel Verbitsky,Rik Westland,Alejandra Perez,Krzysztof Kiryluk,Qingxue Liu,Priya Krithivasan,Adele Mitrotti,David Fasel,Ekaterina Batourina,Matthew G. Sampson,Monica Bodria,Max Werth,Charlly Kao,Jeremiah Martino,Valentina P Capone,Asaf Vivante,Asaf Vivante,Shirlee Shril,Byum Hee Kil,Maddalena Marasa,Jun Zhang,Young Ji Na,Tze Y Lim,Dina Ahram,Patricia L. Weng,Erin L. Heinzen,Alba Carrea,Giorgio Piaggio,Loreto Gesualdo,Valeria Manca,Giuseppe Masnata,Maddalena Gigante,Daniele Cusi,Claudia Izzi,Francesco Scolari,Joanna A.E. van Wijk,Marijan Saraga,Domenico Santoro,Giovanni Conti,Pasquale Zamboli,Hope White,Dorota Drozdz,Katarzyna Zachwieja,Monika Miklaszewska,Marcin Tkaczyk,Daria Tomczyk,Anna Krakowska,Przemysław Sikora,Tomasz Jarmoliński,Maria K Borszewska-Kornacka,Robert Pawluch,Maria Szczepańska,Piotr Adamczyk,Małgorzata Mizerska-Wasiak,Grażyna Krzemień,Agnieszka Szmigielska,Marcin Zaniew,Mark G Dobson,John M Darlow,Prem Puri,David E. Barton,David E. Barton,Susan L. Furth,Bradley A. Warady,Zoran Gucev,Vladimir J Lozanovski,Vladimir J Lozanovski,Velibor Tasic,Isabella Pisani,Landino Allegri,Lida Rodas,Josep M. Campistol,Cécile Jeanpierre,Shumyle Alam,Pasquale Casale,Pasquale Casale,Craig S. Wong,Fangming Lin,Débora Marques de Miranda,Eduardo A. Oliveira,Ana Cristina Simões-e-Silva,Jonathan Barasch,Brynn Levy,Nan Wu,Nan Wu,Friedhelm Hildebrandt,Gian Marco Ghiggeri,Anna Latos-Bielenska,Anna Materna-Kiryluk,Feng Zhang,Hakon Hakonarson,Virginia E. Papaioannou,Cathy Mendelsohn,Ali G. Gharavi,Simone Sanna-Cherchi +94 more
TL;DR: Genome-wide analysis of copy number variants in 2,824 cases across the phenotypic spectrum of CAKUT sheds light on the genomic architecture of disease and identifies TBX6 as a driver forCAKUT subphenotypes in the 16p11.2 microdeletion syndrome.
Journal ArticleDOI
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Esther Lopez-Rivera,Yangfan P. Liu,Miguel Verbitsky,Blair R. Anderson,Valentina P Capone,Edgar A. Otto,Zhonghai Yan,Adele Mitrotti,Jeremiah Martino,Nicholas J Steers,David Fasel,Katarina Vukojević,Rong Deng,Silvia E. Racedo,Qingxue Liu,Max Werth,Rik Westland,Asaf Vivante,Gabriel Makar,Gabriel Makar,Monica Bodria,Matthew G. Sampson,Christopher E. Gillies,Virginia Vega-Warner,Mariarosa Maiorana,Donald Petrey,Barry Honig,Vladimir J Lozanovski,Rémi Salomon,Rémi Salomon,Laurence Heidet,Wassila Carpentier,Dominique Gaillard,Alba Carrea,Loreto Gesualdo,Daniele Cusi,Claudia Izzi,Francesco Scolari,Joanna A.E. van Wijk,Adela Arapović,Mirna Saraga-Babić,Marijan Saraga,Nenad Kunac,Ali Samii,Donna M. McDonald-McGinn,Terrence B. Crowley,Elaine H. Zackai,Dorota Drozdz,Monika Miklaszewska,Marcin Tkaczyk,Przemysław Sikora,Maria Szczepańska,Małgorzata Mizerska-Wasiak,Grażyna Krzemień,Agnieszka Szmigielska,Marcin Zaniew,John M Darlow,Prem Puri,David E. Barton,David E. Barton,Emilio Casolari,Susan L. Furth,Bradley A. Warady,Zoran Gucev,Hakon Hakonarson,Hana Flögelová,Velibor Tasic,Anna Latos-Bielenska,Anna Materna-Kiryluk,Landino Allegri,Craig S. Wong,Iain A. Drummond,V. D’Agati,Akira Imamoto,Jonathan Barasch,Friedhelm Hildebrandt,Krzysztof Kiryluk,Richard P. Lifton,Bernice E. Morrow,Cécile Jeanpierre,Virginia E. Papaioannou,Gian Marco Ghiggeri,Ali G. Gharavi,Nicholas Katsanis,Simone Sanna-Cherchi +84 more
TL;DR: A recurrent 370‐kb deletion at the 22q11.2 locus is identified as a driver of kidney defects in the DiGeorge syndrome and in sporadic congenital kidney and urinary tract anomalies.
Journal ArticleDOI
Perception of health-related quality of life in children with chronic kidney disease by the patients and their caregivers: multicentre national study results.
Katarzyna Kiliś-Pstrusińska,Anna Medyńska,Irena Bałasz Chmielewska,Ryszard Grenda,Agnieszka Kluska-Jóźwiak,Beata Leszczyńska,Julita Niedomagała,Ilona Olszak-Szot,Monika Miklaszewska,Maria Szczepańska,Marcin Tkaczyk,Agnieszka Urzykowska,Anna Wasilewska,Katarzyna Zachwieja,Maria Małgorzata Zajączkowska,Helena Ziółkowska,Ilona Zagozdzon,Danuta Zwolińska +17 more
TL;DR: Children’s lower rating of the quality of life observed by their parents may render the patients unmotivated and adversely affect their adjustment to life in later years, and create conflicts between the parents and the children.
Journal ArticleDOI
The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase ε.
Karolis Azukaitis,Eva Simkova,Mohammad Abdul Majid,Matthias Galiano,Kerstin Benz,Kerstin Amann,Clemens L. Bockmeyer,Radha Gajjar,Kevin E.C. Meyers,Hae Il Cheong,Bärbel Lange-Sperandio,Therese Jungraithmayr,Véronique Frémeaux-Bacchi,Carsten Bergmann,Csaba Bereczki,Monika Miklaszewska,Dorottya Csuka,Zoltán Prohászka,Patrick E. Gipson,Matthew G. Sampson,Mathieu Lemaire,Franz Schaefer +21 more
TL;DR: Most patients presented with HUS accompanied by proteinuria, whereas a subset of patients exhibited clinical and histologic patterns of MPGN without TMA, suggesting additional factors mediating phenotypic heterogeneity.
Journal ArticleDOI
Oxidative Stress Biomarkers and Left Ventricular Hypertrophy in Children with Chronic Kidney Disease.
Dorota Drozdz,Przemko Kwinta,Krystyna Sztefko,Zbigniew Kordon,Tomasz Dróżdż,Monika Łątka,Monika Miklaszewska,Katarzyna Zachwieja,Andrzej Rudziński,Jacek A Pietrzyk +9 more
TL;DR: Hypertension and dyslipidemia correlated with lipid oxidation in children with CKD, and oxLDLs seem to be valuable markers of oxidative stress in CKD patients, correlating with left ventricular hypertrophy.