Hasil Pencarian - Velibor Tasic

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  1. 1
    Neutrophil Gelatinase-Associated Lipocalin as an Early Biomarker of Acute Kidney Injury in Newborns

    Neutrophil Gelatinase-Associated Lipocalin as an Early Biomarker of Acute Kidney Injury in Newborns oleh Silvana Naunova-Timovska, Svetlana Cekovska, Emilija Sahpazova, Velibor Tasić

    Diterbitkan 2020-01-01
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  2. 2
    A Patient with Unilateral Tibial Aplasia and Accessory Scrotum: A Pure Coincidence or Nonfortuitous Association?

    A Patient with Unilateral Tibial Aplasia and Accessory Scrotum: A Pure Coincidence or Nonfortuitous Association? oleh Zoran Gucev, Marco Castori, Velibor Tasic, Nada Popjordanova, Arijeta Hasani

    Diterbitkan 2010-01-01
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  3. 3
    The implications of complexity, systems thinking and philosophy for pediatricians

    The implications of complexity, systems thinking and philosophy for pediatricians oleh Jochen Ehrich, Jürgen Manemann, Velibor Tasic, Natale Gaspare DeSanto

    Diterbitkan 2021-03-01
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  4. 4
    The Rationale of Complement Blockade of the MCP<sub>ggaac</sub> Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review

    The Rationale of Complement Blockade of the MCP<sub>ggaac</sub> Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Re... oleh Daniel Turudic, Danka Pokrajac, Velibor Tasic, Dino Kasumovic, Zoltan Prohaszka, Danko Milosevic

    Diterbitkan 2023-08-01
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  5. 5
    Friedreich Ataxia (Fa) Associated with Diabetes Mellitus Type 1 and Hyperthrophic Cardiomyopathy

    Friedreich Ataxia (Fa) Associated with Diabetes Mellitus Type 1 and Hyperthrophic Cardiomyopathy oleh Zoran Gucev, Velibor Tasic, Aleksandra Jancevska, Nada Popjordanova, Svetlana Koceva, Marija Kuturec, Vesna Sabolic

    Diterbitkan 2009-05-01
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  6. 6
    Pulsed-field gel electrophoresis used for typing of extended-spectrum-β-lactamases- producing Escherichia coli Isolated from infant ҆ s respiratory and digestive system

    Pulsed-field gel electrophoresis used for typing of extended-spectrum-β-lactamases- producing Escherichia coli Isolated from infant ҆ s respiratory and digestive system oleh Gorica Popova, Dean Jankuloski, Benjamin Felix, Katerina Boskovska, Biljana Stojanovska - Dimzovska, Velibor Tasic, Katerina Blagoevska

    Diterbitkan 2018-10-01
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  7. 7
    Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population

    Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population oleh Blanka Stiburkova, Jana Bohatá, Kateřina Pavelcová, Velibor Tasic, Dijana Plaseska-Karanfilska, Sung-Kweon Cho, Ludmila Potočnaková, Jana Šaligová

    Diterbitkan 2021-11-01
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  8. 8
    Universal Health Coverage “Leave No Child Behind”

    Universal Health Coverage “Leave No Child Behind” oleh Liesbeth Siderius, David Neubauer, Anjan Bhattacharya, Péter Altorjai, Lali Margvelashvili, Sanath Lamabadusuriya, Jolanta Wierzba, Artur Mazur, Piotr Albrecht, Velibor Tasic

    Diterbitkan 2021-03-01
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  9. 9
    Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans

    Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans oleh Aleksandra Stajkovska, Sanja Mehandziska, Margarita Stavrevska, Kristina Jakovleva, Natasha Nikchevska, Zan Mitrev, Ivan Kungulovski, Gjorgje Zafiroski, Velibor Tasic, Goran Kungulovski

    Diterbitkan 2018-04-01
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  10. 10
    Clinical and functional characterization of URAT1 variants.

    Clinical and functional characterization of URAT1 variants. oleh Velibor Tasic, Ann Marie Hynes, Kenichiro Kitamura, Hae Il Cheong, Vladimir J Lozanovski, Zoran Gucev, Promsuk Jutabha, Naohiko Anzai, John A Sayer

    Diterbitkan 2011-01-01
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  11. 11
    Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic Testing

    Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic Testing oleh Michaela Stippel, Korbinian M. Riedhammer, Korbinian M. Riedhammer, Bärbel Lange-Sperandio, Michaela Geßner, Matthias C. Braunisch, Matthias C. Braunisch, Roman Günthner, Roman Günthner, Martin Bald, Miriam Schmidts, Peter Strotmann, Velibor Tasic, Christoph Schmaderer, Lutz Renders, Uwe Heemann, Julia Hoefele

    Diterbitkan 2021-05-01
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  12. 12
    Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2

    Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2 oleh Yu Toyoda, Sung Kweon Cho, Sung Kweon Cho, Velibor Tasic, Kateřina Pavelcová, Jana Bohatá, Hiroshi Suzuki, Victor A. David, Jaeho Yoon, Anna Pallaiova, Jana Šaligová, Darryl Nousome, Raul Cachau, Cheryl A. Winkler, Tappei Takada, Blanka Stibůrková, Blanka Stibůrková, Blanka Stibůrková

    Diterbitkan 2023-01-01
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  13. 13
    Worldwide view of nephropathic cystinosis: results from a survey from 30 countries

    Worldwide view of nephropathic cystinosis: results from a survey from 30 countries oleh Aurélia Bertholet-Thomas, Julien Berthiller, Velibor Tasic, Behrouz Kassai, Hasan Otukesh, Marcella Greco, Jochen Ehrich, Rejane de Paula Bernardes, Georges Deschênes, Sally-Ann Hulton, Michel Fischbach, Kenza Soulami, Bassam Saeed, Ehsan Valavi, Carlos Jose Cobenas, Bülent Hacihamdioglu, Gabrielle Weiler, Pierre Cochat, Justine Bacchetta

    Diterbitkan 2017-07-01
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  14. 14
    The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy—A human genetics department experience

    The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy—A human genetics department experience oleh Jasmina Ćomić, Jasmina Ćomić, Korbinian M. Riedhammer, Korbinian M. Riedhammer, Roman Günthner, Christian W. Schaaf, Christian W. Schaaf, Patrick Richthammer, Hannes Simmendinger, Donald Kieffer, Riccardo Berutti, Velibor Tasic, Nora Abazi-Emini, Valbona Nushi-Stavileci, Jovana Putnik, Nataša Stajic, Adrian Lungu, Oliver Gross, Lutz Renders, Uwe Heemann, Matthias C. Braunisch, Thomas Meitinger, Julia Hoefele

    Diterbitkan 2022-08-01
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  15. 15
    A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux.

    A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux. oleh Amelie T van der Ven, Birgit Kobbe, Stefan Kohl, Shirlee Shril, Hans-Martin Pogoda, Thomas Imhof, Hadas Ityel, Asaf Vivante, Jing Chen, Daw-Yang Hwang, Dervla M Connaughton, Nina Mann, Eugen Widmeier, Mary Taglienti, Johanna Magdalena Schmidt, Makiko Nakayama, Prabha Senguttuvan, Selvin Kumar, Velibor Tasic, Elijah O Kehinde, Shrikant M Mane, Richard P Lifton, Neveen Soliman, Weining Lu, Stuart B Bauer, Matthias Hammerschmidt, Raimund Wagener, Friedhelm Hildebrandt

    Diterbitkan 2018-01-01
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  16. 16
    Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions

    Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions oleh Konstantin Deutsch, Verena Klämbt, Thomas M. Kitzler, Tilman Jobst-Schwan, Ronen Schneider, Florian Buerger, Steve Seltzsam, Sherif El Desoky, Jameela A. Kari, Farkhanda Hafeez, Maria Szczepańska, Loai A. Eid, Hazem S. Awad, Muna Al-Saffar, Neveen A. Soliman, Velibor Tasic, Camille Nicolas-Frank, Kirollos Yousef, Luca M. Schierbaum, Sophia Schneider, Abdul Halawi, Izzeldin Elmubarak, Katharina Lemberg, Shirlee Shril, Shrikant M. Mane, Nancy Rodig, Friedhelm Hildebrandt

    Diterbitkan 2024-09-01
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  17. 17
    Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age

    Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age oleh Roman Günthner, Roman Günthner, Lea Knipping, Stefanie Jeruschke, Robin Satanoskij, Bettina Lorenz-Depiereux, Clara Hemmer, Matthias C. Braunisch, Matthias C. Braunisch, Korbinian M. Riedhammer, Korbinian M. Riedhammer, Jasmina Ćomić, Jasmina Ćomić, Burkhard Tönshoff, Velibor Tasic, Nora Abazi-Emini, Valbona Nushi-Stavileci, Karin Buiting, Nikola Gjorgjievski, Ana Momirovska, Ludwig Patzer, Martin Kirschstein, Oliver Gross, Adrian Lungu, Stefanie Weber, Lutz Renders, Uwe Heemann, Thomas Meitinger, Anja K. Büscher, Julia Hoefele

    Diterbitkan 2022-10-01
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  18. 18
    Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract

    Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract oleh Chen-Han Wilfred Wu, Tze Y. Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum, Sophia Schneider, Nina Mann, Dervla M. Connaughton, Makiko Nakayama, Amelie T. van der Ven, Rufeng Dai, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Natasa Stajic, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan M. Fathy, Danko Milosevic, Daniel Turudic, Muna Al Saffar, Hazem S. Awad, Loai A. Eid, Aravind Ramanathan, Prabha Senguttuvan, Shrikant M. Mane, Richard S. Lee, Stuart B. Bauer, Weining Lu, Alina C. Hilger, Velibor Tasic, Shirlee Shril, Simone Sanna-Cherchi, Friedhelm Hildebrandt

    Diterbitkan 2022-10-01
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  19. 19
    Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus

    Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus oleh Simon H. Jiang, Vicki Athanasopoulos, Julia I. Ellyard, Aaron Chuah, Jean Cappello, Amelia Cook, Savit B. Prabhu, Jacob Cardenas, Jinghua Gu, Maurice Stanley, Jonathan A. Roco, Ilenia Papa, Mehmet Yabas, Giles D. Walters, Gaetan Burgio, Kathryn McKeon, James M. Byers, Charlotte Burrin, Anselm Enders, Lisa A. Miosge, Pablo F. Canete, Marija Jelusic, Velibor Tasic, Adrian C. Lungu, Stephen I. Alexander, Arthur R. Kitching, David A. Fulcher, Nan Shen, Todor Arsov, Paul A. Gatenby, Jeff J. Babon, Dominic F. Mallon, Carmen de Lucas Collantes, Eric A. Stone, Philip Wu, Matthew A. Field, Thomas D. Andrews, Eun Cho, Virginia Pascual, Matthew C. Cook, Carola G. Vinuesa

    Diterbitkan 2019-05-01
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  20. 20
    Diversity of kidney care referral pathways in national child health systems of 48 European countries

    Diversity of kidney care referral pathways in national child health systems of 48 European countries oleh 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

    Diterbitkan 2024-01-01
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