Torthaí cuardaigh - Velibor Tasic

Beachtaigh na torthaí
  1. 1
    Post-streptococcal Glomerulonephritis in Hong Kong

    Post-streptococcal Glomerulonephritis in Hong Kong de réir Velibor, Tasić, Kuzmanovska, Dafina, Sajkovski, Aleksander

    Foilsithe / Cruthaithe 1988
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  2. 2
    Obesity in Childhood and Adolescence, Genetic Factors

    Obesity in Childhood and Adolescence, Genetic Factors de réir Marko Kostovski, Velibor Tasić, Nevena Laban, Momir Polenaković, Dragan Danilovski, Zoran Gucev

    Foilsithe / Cruthaithe 2017
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  3. 3
    As implicações da complexidade, sistemas de pensamento e filosofia para pediatras

    As implicações da complexidade, sistemas de pensamento e filosofia para pediatras de réir J. H. H. Ehrich, Jürgen Manemann, Velibor Tasić, Natale G. DeSanto, Barbara Rodrigues Barbosa

    Foilsithe / Cruthaithe 2021
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  4. 4
    Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder

    Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder de réir Zoran Gucev, Velibor Tasić, Aleksandra Jančevska, Marina Krstevska Konstantinova, Nada Pop‐Jordanova, Zoran Trajkovski, Leslie G. Biesecker

    Foilsithe / Cruthaithe 2008
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  5. 5
    Renal Phenotype in Lowe Syndrome

    Renal Phenotype in Lowe Syndrome de réir Detlef Böckenhauer, Arend Bökenkamp, William van’t Hoff, Elena Levtchenko, Joana E. Kist‐van Holthe, Velibor Tasic, Michael Ludwig

    Foilsithe / Cruthaithe 2008
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  6. 6
    Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets

    Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets de réir Peter J. Malloy, Velibor Tasić, Doris Taha, Filiz Tütüncüler, Goh Siok Ying, Loke Kah Yin, Jining Wang, David Feldman

    Foilsithe / Cruthaithe 2013
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  7. 7
    Clinical and Functional Characterization of URAT1 Variants

    Clinical and Functional Characterization of URAT1 Variants de réir Velibor Tasić, Ann Marie Hynes, Kenichiro Kitamura, Hae Il Cheong, Vladimir J. Lozanovski, Zoran Gucev, Promsuk Jutabha, Naohiko Anzai, John A. Sayer

    Foilsithe / Cruthaithe 2011
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  8. 8
    Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

    Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis de réir Pawaree Saisawat, Velibor Tasić, Virginia Vega-Warner, Elijah O. Kehinde, Barbara Günther, Rannar Airik, Jeffrey W. Innis, Bethan E. Hoskins, Julia Hoefele, Edgar A. Otto, Friedhelm Hildebrandt

    Foilsithe / Cruthaithe 2011
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  9. 9
    Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion

    Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion de réir Joaquim Calado, Yves Sznajer, Daniel L. Metzger, Ana Rita, Marie C. Hogan, Antonios Kattamis, M. Scharf, Velibor Tasić, Johann Greil, Florian Brinkert, Markus J. Kemper, René Santer

    Foilsithe / Cruthaithe 2008
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  10. 10
    Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract

    Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract de réir Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Alina C. Hilger, Pawaree Saisawat, Asaf Vivante, Nataša Stajić, Radovan Bogdanović, Heiko Reutter, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt

    Foilsithe / Cruthaithe 2014
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  11. 11
    Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract

    Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract de réir Daw‐Yang Hwang, Gabriel C. Dworschak, Stefan Kohl, Pawaree Saisawat, Asaf Vivante, Alina C. Hilger, Heiko Reutter, Neveen A. Soliman, Radovan Bogdanović, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt

    Foilsithe / Cruthaithe 2014
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  12. 12
    Dent Disease with Mutations in OCRL1

    Dent Disease with Mutations in OCRL1 de réir R R Hoopes, Antony E. Shrimpton, Stephen J. Knohl, Paul Hueber, Bernd Höppe, János Mátyus, Ari M. Simckes, Velibor Tasic, Burkhard Toenshoff, Sharon F. Suchy, Robert L. Nussbaum, Steven J. Scheinman

    Foilsithe / Cruthaithe 2005
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  13. 13
    Clinical, biochemical, and pathophysiological analysis of <i>SLC34A1</i> mutations

    Clinical, biochemical, and pathophysiological analysis of <i>SLC34A1</i> mutations de réir Amy Fearn, Benjamin Allison, Sarah J. Rice, Noel Edwards, Jan Halbritter, Soline Bourgeois, Eva M. Pastor‐Arroyo, Friedhelm Hildebrandt, Velibor Tasić, Carsten A. Wagner, Nati Hernando, John A. Sayer, Andreas Werner

    Foilsithe / Cruthaithe 2018
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  14. 14
    Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6

    Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6 de réir Duncan B. Sparrow, Aideen M. McInerney‐Leo, Zoran Gucev, Brooke Gardiner, Mhairi Marshall, Paul Leo, Deborah L. Chapman, Velibor Tasić, Abduhadi Shishko, Matthew A. Brown, Emma L. Duncan, Sally L. Dunwoodie

    Foilsithe / Cruthaithe 2013
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  15. 15
    Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract

    Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract de réir Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl, Jing Chen, Shirlee Shril, Julian Schulz, Amelie van der Ven, Ghaleb H. Daouk, Neveen A. Soliman, Aravind Selvin Kumar, Prabha Senguttuvan, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt

    Foilsithe / Cruthaithe 2016
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  16. 16
    Fourteen Monogenic Genes Account for 15% of Nephrolithiasis/Nephrocalcinosis

    Fourteen Monogenic Genes Account for 15% of Nephrolithiasis/Nephrocalcinosis de réir Jan Halbritter, Michelle A. Baum, Ann Marie Hynes, Sarah J. Rice, David T. Thwaites, Zoran Gucev, Brittany Fisher, Leslie Spaneas, Jonathan D. Porath, Daniela A. Braun, Ari J. Wassner, Caleb P. Nelson, Velibor Tasić, John A. Sayer, Friedhelm Hildebrandt

    Foilsithe / Cruthaithe 2014
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  17. 17
    Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

    Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis de réir Stefanie Weber, Linda Schneider, Melanie Peters, Joachim Misselwitz, Gabriele Rönnefarth, M. Böswald, Klaus E. Bonzel, Tomáš Seeman, Tereza Šuláková, Eberhard Kuwertz-Bröking, Alojz Gregorič, Jean‐Bernard Palcoux, Velibor Tasić, Friedrich Manz, K Schärer, Hannsjörg W. Seyberth, Martin Konrad

    Foilsithe / Cruthaithe 2001
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  18. 18
    CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

    CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis de réir Martin Konrad, Jianghui Hou, Stefanie Weber, JoCombining Diaeresisrg DoCombining Diaeresistsch, Jameela A. Kari, Tomáš Seeman, Eberhard Kuwertz-BroCombining Diaeresisking, Amira Peco‐Antić, Velibor Tasić, Katalin Dittrich, Hammad O. Alshaya, Rodo O. von Vigier, Sabina Gallati, Daniel A. Goodenough, André Schaller

    Foilsithe / Cruthaithe 2007
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  19. 19
    Distal renal tubular acidosis: ERKNet/ESPN clinical practice points

    Distal renal tubular acidosis: ERKNet/ESPN clinical practice points de réir Francesco Trepiccione, Steven Walsh, Gema Ariceta, Olivia Boyer, Francesco Emma, Roberta Camilla, Pietro Manuel Ferraro, Dieter Haffner, Martin Konrad, Elena Levtchenko, Sergio Camilo Lopez-Garcia, Fernando Santos, Stella Stabouli, Maria Szczepańska, Velibor Tasić, Rezan Topaloĝlu, Rosa Vargas‐Poussou, Tanja Wlodkowski, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2021
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  20. 20
    Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis

    Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis de réir Daniela A. Braun, Jennifer A. Lawson, Heon Yung Gee, Jan Halbritter, Shirlee Shril, Weizhen Tan, Deborah R. Stein, Ari J. Wassner, Michael A. Ferguson, Zoran Gucev, Brittany Fisher, Leslie Spaneas, Jennifer D. Varner, John A. Sayer, Danko Milošević, Michelle A. Baum, Velibor Tasić, Friedhelm Hildebrandt

    Foilsithe / Cruthaithe 2016
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