Your browser doesn't support javascript.
loading
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.
Viering, Daan; Schlingmann, Karl P; Hureaux, Marguerite; Nijenhuis, Tom; Mallett, Andrew; Chan, Melanie M Y; van Beek, André; van Eerde, Albertien M; Coulibaly, Jean-Marie; Vallet, Marion; Decramer, Stéphane; Pelletier, Solenne; Klaus, Günter; Kömhoff, Martin; Beetz, Rolf; Patel, Chirag; Shenoy, Mohan; Steenbergen, Eric J; Anderson, Glenn; Bongers, Ernie M H F; Bergmann, Carsten; Panneman, Daan; Rodenburg, Richard J; Kleta, Robert; Houillier, Pascal; Konrad, Martin; Vargas-Poussou, Rosa; Knoers, Nine V A M; Bockenhauer, Detlef; de Baaij, Jeroen H F.
Affiliation
  • Viering D; Department of Physiology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Schlingmann KP; Department of General Pediatrics, University Children's Hospital, Münster, Germany.
  • Hureaux M; Reference Center for Hereditary Kidney and Childhood Diseases (Maladies rénales héréditaires de l'enfant et de l'adulte [MARHEA]), Paris, France.
  • Nijenhuis T; Department of Genetics, Assistance Publique Hôpitaux de Paris, Hôpital Européen Georges-Pompidou, Paris, France.
  • Mallett A; Department of Nephrology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Chan MMY; Department of Renal Medicine, Townsville University Hospital, Townsville, Australia.
  • van Beek A; Queensland Conjoint Renal Genetics Service - Genetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Australia.
  • van Eerde AM; Department of Renal Medicine, University College London, London, United Kingdom.
  • Coulibaly JM; Department of Endocrinology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Vallet M; Genetics Department, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Decramer S; Service of Nephrology, Yves Le Foll Hospital, Saint Brieuc, France.
  • Pelletier S; Department of Physiological Functional Investigations, Centre Hospitalier Universitaire de Toulouse, Université Paul Sabatier, Toulouse, France.
  • Klaus G; Pediatric Nephrology, Internal Medicine and Rheumatology, Southwest Renal Rare Diseases Centre (SORARE), University Children's Hospital, Toulouse, France.
  • Kömhoff M; Department of Nephrology, University Hospital-Lyon Sud, Lyon, France.
  • Beetz R; Kuratorium für Heimdialyse Pediatric Kidney Center, Marburg, Germany.
  • Patel C; University Children's Hospital, Philipps-University, Marburg, Germany.
  • Shenoy M; Johannes Gutenberg Universität Mainz, Zentrum für Kinder- und Jugendmedizin, Mainz, Germany.
  • Steenbergen EJ; Queensland Conjoint Renal Genetics Service - Genetic Health Queensland, Royal Brisbane and Women's Hospital, Brisbane, Australia.
  • Anderson G; Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester, United Kingdom.
  • Bongers EMHF; Department of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Bergmann C; Department of Pathology, Great Ormond Street Hospital for Children National Health Service (NHS) Foundation Trust, London, United Kingdom.
  • Panneman D; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Rodenburg RJ; Limbach Genetics, Medizinische Genetik Mainz, Prof. Bergmann & Kollegen, Mainz, Germany.
  • Kleta R; Department of Medicine, Division of Nephrology, University Hospital Freiburg, Germany.
  • Houillier P; Radboud Center for Mitochondrial Medicine, Translational Metabolic Laboratory, Department of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Konrad M; Radboud Center for Mitochondrial Medicine, Translational Metabolic Laboratory, Department of Pediatrics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Vargas-Poussou R; Department of Renal Medicine, University College London, London, United Kingdom.
  • Knoers NVAM; Department of Paediatric Nephrology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
  • Bockenhauer D; Reference Center for Hereditary Kidney and Childhood Diseases (Maladies rénales héréditaires de l'enfant et de l'adulte [MARHEA]), Paris, France.
  • de Baaij JHF; Centre de Recherche des Cordeliers, Sorbonne Université, Institut National de la Santé et de Recherche Médicale (INSERM), Université de Paris, Centre National de la Recherche Scientifique (CNRS), Paris, France.
J Am Soc Nephrol ; 33(2): 305-325, 2022 02.
Article in En | MEDLINE | ID: mdl-34607911
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Gitelman Syndrome / Mutation Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Am Soc Nephrol Journal subject: NEFROLOGIA Year: 2022 Document type: Article Affiliation country: Países Bajos
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Gitelman Syndrome / Mutation Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Am Soc Nephrol Journal subject: NEFROLOGIA Year: 2022 Document type: Article Affiliation country: Países Bajos