Torthaí cuardaigh - Detlef Böckenhauer

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  1. 1
    Bartter Syndromes and Other Salt-Losing Tubulopathies

    Bartter Syndromes and Other Salt-Losing Tubulopathies de réir Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2006
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  2. 2
    Salt-Losing Tubulopathies in Children: What’s New, What’s Controversial?

    Salt-Losing Tubulopathies in Children: What’s New, What’s Controversial? de réir Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2017
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  3. 3
    Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus

    Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus de réir Detlef Böckenhauer, Daniel G. Bichet

    Foilsithe / Cruthaithe 2015
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  4. 4
    Bartter and Gitelman syndromes: Questions of class

    Bartter and Gitelman syndromes: Questions of class de réir Martine Besouw, Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2019
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  5. 5
    KCNK2: reversible conversion of a hippocampal potassium leak into a voltage-dependent channel

    KCNK2: reversible conversion of a hippocampal potassium leak into a voltage-dependent channel de réir Detlef Böckenhauer, Noam Zilberberg, Steven A. Goldstein

    Foilsithe / Cruthaithe 2001
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  6. 6
    Zebrafish as a model for kidney function and disease

    Zebrafish as a model for kidney function and disease de réir Priya Outtandy, Claire Russell, Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2018
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  7. 7
    Genetic, pathophysiological, and clinical aspects of nephrocalcinosis

    Genetic, pathophysiological, and clinical aspects of nephrocalcinosis de réir Ben Oliveira, Robert Kleta, Detlef Böckenhauer, Stephen B. Walsh

    Foilsithe / Cruthaithe 2016
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  8. 8
    Potassium leak channels and the KCNK family of two-p-domain subunits

    Potassium leak channels and the KCNK family of two-p-domain subunits de réir Steven A. Goldstein, Detlef Böckenhauer, Anne M. Kelly, Noam Zilberberg

    Foilsithe / Cruthaithe 2001
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  9. 9
    EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10

    EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10 de réir Ola Abdelhadi, Daniela Iancu, Horia Stanescu, Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2016
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  10. 10
    Inherited Tubulopathies of the Kidney

    Inherited Tubulopathies of the Kidney de réir Mallory L. Downie, Sergio Camilo Lopez-Garcia, Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2020
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  11. 11
    The orthopaedic management of lower limb deformity in hypophosphataemic rickets

    The orthopaedic management of lower limb deformity in hypophosphataemic rickets de réir A Horn, Jonathan Wright, Detlef Böckenhauer, William van’t Hoff, Deborah M. Eastwood

    Foilsithe / Cruthaithe 2017
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  12. 12
    Epilepsy in kcnj10 Morphant Zebrafish Assessed with a Novel Method for Long-Term EEG Recordings

    Epilepsy in kcnj10 Morphant Zebrafish Assessed with a Novel Method for Long-Term EEG Recordings de réir Anselm A. Zdebik, Fahad Mahmood, Horia Stanescu, Robert Kleta, Detlef Böckenhauer, Claire Russell

    Foilsithe / Cruthaithe 2013
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  13. 13
    Renal Fanconi syndrome: taking a proximal look at the nephron

    Renal Fanconi syndrome: taking a proximal look at the nephron de réir Enriko Klootwijk, Markus Reichold, Robert J. Unwin, Robert Kleta, Richard Warth, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2014
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  14. 14
    Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK

    Epidemiology of paediatric renal stone disease: a 22-year single centre experience in the UK de réir Naomi Issler, Stephanie Dufek, Robert Kleta, Detlef Böckenhauer, Naima Smeulders, William van’t Hoff

    Foilsithe / Cruthaithe 2017
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  15. 15
    Mitochondrial DNA mutations in renal disease: an overview

    Mitochondrial DNA mutations in renal disease: an overview de réir Larissa P. Govers, Hakan R. Toka, Ali Hariri, Stephen B. Walsh, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2020
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  16. 16
    Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases

    Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases de réir Detlef Böckenhauer, William van’t Hoff, Mehul Dattani, A. Lehnhardt, M.S. Subtirelu, Friedhelm Hildebrandt, Daniel G. Bichet

    Foilsithe / Cruthaithe 2010
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  17. 17
    Genetic causes of hypomagnesemia, a clinical overview

    Genetic causes of hypomagnesemia, a clinical overview de réir Daan H.H.M. Viering, Jeroen H. F. de Baaij, Stephen B. Walsh, Robert Kleta, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2016
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  18. 18
    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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  19. 19
    Novel OCRL mutations in patients with Dent-2 disease

    Novel OCRL mutations in patients with Dent-2 disease de réir Detlef Böckenhauer, Arend Bökenkamp, Matti Nuutinen, Robert J. Unwin, William van’t Hoff, Tony Sirimanna, Kristina Vrljičak, Michael Ludwig

    Foilsithe / Cruthaithe 2015
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  20. 20
    Clinical and diagnostic features of Bartter and Gitelman syndromes

    Clinical and diagnostic features of Bartter and Gitelman syndromes de réir Patrick R. Walsh, Yincent Tse, Emma Ashton, Daniela Iancu, Lucy Jenkins, Marc Bienias, Robert Kleta, William van’t Hoff, Detlef Böckenhauer

    Foilsithe / Cruthaithe 2017
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