檢索結果 - Detlef Böckenhauer

Refine Results
  1. 1
    Bartter Syndromes and Other Salt-Losing Tubulopathies

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

    出版 2006
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  2. 2
    Salt-Losing Tubulopathies in Children: What’s New, What’s Controversial?

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

    出版 2017
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  3. 3
    Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus

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

    出版 2015
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  4. 4
    Bartter and Gitelman syndromes: Questions of class

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

    出版 2019
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  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 由 Detlef Böckenhauer, Noam Zilberberg, Steven A. Goldstein

    出版 2001
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  6. 6
    Zebrafish as a model for kidney function and disease

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

    出版 2018
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  7. 7
    Genetic, pathophysiological, and clinical aspects of nephrocalcinosis

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

    出版 2016
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  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 由 Steven A. Goldstein, Detlef Böckenhauer, Anne M. Kelly, Noam Zilberberg

    出版 2001
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  9. 9
    EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10

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

    出版 2016
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  10. 10
    Inherited Tubulopathies of the Kidney

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

    出版 2020
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  11. 11
    The orthopaedic management of lower limb deformity in hypophosphataemic rickets

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

    出版 2017
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 Anselm A. Zdebik, Fahad Mahmood, Horia Stanescu, Robert Kleta, Detlef Böckenhauer, Claire Russell

    出版 2013
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  13. 13
    Renal Fanconi syndrome: taking a proximal look at the nephron

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

    出版 2014
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  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 由 Naomi Issler, Stephanie Dufek, Robert Kleta, Detlef Böckenhauer, Naima Smeulders, William van’t Hoff

    出版 2017
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:
  15. 15
    Mitochondrial DNA mutations in renal disease: an overview

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

    出版 2020
    獲取全文 獲取全文
    Revisão
    加到收藏夾
    Saved in:
  16. 16
    Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases

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

    出版 2010
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  17. 17
    Genetic causes of hypomagnesemia, a clinical overview

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

    出版 2016
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  18. 18
    Renal Phenotype in Lowe Syndrome

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

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  19. 19
    Novel OCRL mutations in patients with Dent-2 disease

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

    出版 2015
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  20. 20
    Clinical and diagnostic features of Bartter and Gitelman syndromes

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

    出版 2017
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: