ArticleJournal of the American Society of Nephrology : JASN2017
Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
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Article in Journal of the American Society of Nephrology : JASN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.
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50citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
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Who cites it
50 citing papers in PubMed, 118 citations in OpenAlex.
- Adjunctive acetazolamide therapy for the treatment of Bartter syndrome.International urology and nephrology · 2020Trial
- Copeptin in the diagnosis and management of renal tubular disorders.Pediatric nephrology (Berlin, Germany) · 2026Review
- Gitelman Syndrome in a Child Presenting With Polyuria and Polydipsia: Diagnostic Challenges in a Resource-Limited Setting.Case reports in nephrology · 2026Article
- An Atypical Presentation of Bartter Syndrome Type 3 With Hypocalciuria and Opisthotonus Posture in a Preterm Infant.Clinical case reports · 2025Article
- Fetal umbilical vein thrombosis associated with fetal bartter syndrome: an unusual case report and literature review.BMC pregnancy and childbirth · 2025Review
- Genetic background of neonatal hypokalemia.Pediatric nephrology (Berlin, Germany) · 2025Review
- Integrated transcriptomic and single-cell RNA-seq analysis identifies CLCNKB, KLK1 and PLEKHA4 as key gene of AKI-to-CKD progression.Frontiers in immunology · 2025Article
- Article
- Clinical, genetic characteristics and outcome of four Chinese patients with Bartter syndrome type 3: Further insight into a genotype-phenotype correlation.Molecular genetics and metabolism reports · 2024Article
- ClC-K Kidney Chloride Channels: From Structure to Pathology.Handbook of experimental pharmacology · 2024Article
- Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.Genome medicine · 2023Article
- Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3.Scientific reports · 2023Article
- Genetic diagnosis and treatment of hereditary renal tubular disease with hypokalemia and alkalosis.Journal of nephrology · 2023Review
- Bartter syndrome type III with glomerular dysplasia and chronic kidney disease: A case report.Frontiers in pediatrics · 2023Review
- Bartter Syndrome: Perspectives of a Pediatric Nephrologist.Electrolyte & blood pressure : E & BP · 2022Review
- Model organisms for functional validation in genetic renal disease.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2022Article
- Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygousClinical case reports · 2022Article
- Potassium and the kidney: a reciprocal relationship with clinical relevance.Pediatric nephrology (Berlin, Germany) · 2022Review
- The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing.Journal of the Endocrine Society · 2022Article
- A novel mutation of KCNJ1 identified in an affected child with nephrolithiasis.BMC nephrology · 2022Article
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Authors and funding
39 authors at 20 institutions in 4 countries.
Elsa SeysPediatric Nephrology Unit, American Memorial Hospital, Reims University Hospital, Reims, France.
Olga AndriniUnité Mixte de Recherche en Santé 1138, Team 3, Université Pierre et Marie Curie, Paris, France.
Mathilde KeckUnité Mixte de Recherche en Santé 1138, Team 3, Université Pierre et Marie Curie, Paris, France.
Lamisse Mansour-HendiliFaculté de Médecine, Université Paris Descartes, Paris, France.
Pierre-Yves CourandCentre d'Investigation Clinique, Hôpital Européen Georges Pompidou, Assistance Publique-Hôpitaux de Paris, Paris, France.
Christophe SimianDepartment of Genetics and.
Georges DeschenesPediatric Nephrology Unit, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France.
Theresa KwonPediatric Nephrology Unit, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris, France.
Aurélia Bertholet-ThomasNéphrogones, Centre de Référence des Maladies Rénales Rares, Pediatric Nephrology, Rhumatology and Dermatology Unit, Hôpital Femme-Mère-Enfant and.
Guillaume BobrieNephrology Unit, Clinique du Vert Galant, Tremblay-en-France, France.
Jean Sébastien BordeNephrology Unit, Centre hospitalier de Saintonge, Saintes, France.
Guylhène Bourdat-MichelDepartement of Pediatrics, Centre Hospitalier Universitaire de Grenoble, Grenoble, France.
Stéphane DecramerDepartement of Pediatrics and.
Mathilde CailliezPediatric Nephrology Unit, Hôpital de la Timone, Assistance Publique des Hôpitaux de Marseille, Marseille, France.
Pauline KrugCentre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte, Paris, France.
Paul CozetteNephrology Unit, Centre Hospitalier du Pays d'Aix, Aix-en-Provence, France.
Jean Daniel DelbetPediatric Nephrology Unit, Hôpital Trousseau, Assistance Publique des Hôpitaux de Paris, Paris, France.
Laurence DubourgExploration Fonctionnelle Rénale et Métabolique, Groupement Hospitalier est Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Dominique ChaveauDepartement of Nephrology, Centre de Référence des Maladies Rénales Rares du Sud-Ouest, Hôpital de Toulouse, Université Paul Sabatier, Toulouse, France.
Marc FilaPediatric Nephrology Unit, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
Noémie Jourde-ChicheFaculté de Médecine, Centre de Référence des Maladies Rénales Rares du Sud-Ouest, Aix-MarseilleUniversité-Vascular Research Center of Marseille, Marseille, France.
Bertrand KnebelmannCentre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte, Paris, France.
Marie-Pierre LavocatDepartement of Pediatrics, Hôpital Nord, Centre Hospitalier Universitaire de Saint Etienne, Saint Etienne, France.
Sandrine LemoineExploration Fonctionnelle Rénale et Métabolique, Groupement Hospitalier est Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Djamal DjeddiDepartment of Pediatrics and Adolescent Medicine, Centre Hospitalier Universitaire d'Amiens, Amiens, France.
Brigitte LlanasService de Néphrologie Pédiatrique, Groupement Hospitalier Pellegrin, Centre Hospitalier Universitaire de Bordeaux, Centre de Référence des Maladies Rénales Rares du Sud-Ouest, Bordeaux, France.
Ferielle LouilletDepartment of Pediatrics, Centre Hospitalier Universitaire Charles Nicolle, Rouen, France.
Elodie MerieauNephrology Unit,Centre Hospitalier Universitaire Tours, Tours, France.
Maria MilevaDepartment of Pediatrics, Centre Hospitalier Pierre Oudot de Bourgoin-Jallieu, Bourgoin-Jallieu, France.
Luisa Mota-VieiraMolecular Genetics Unit, Hospital do Divino Espírito Santo de Ponta Delgada, Entidade Pública Empresarial Regional, Açores, Portugal.
Christiane MoussonNephrology Unit, Centre Hospitalier Universitaire de Dijon, Dijon, France.
François NobiliPediatric Nephrology Unit, Centre Hospitalier Universitaire de Besançon, Besançon, France.
Robert NovoPediatric Nephrology Unit, Hôpital Jeanne de Flandre, Centre Hospitalier Universitaire de Lille, Lille, France.
Gwenaëlle Roussey-KeslerPediatric Nephrology Unit, Centre Hospitalier Universitaire de Nantes, Nantes, France.
Isabelle VrillonPediatric Nephrology Unit, Hôpitaux de Brabois, Centre Hospitalier Universitaire de Nancy, Vandoeuvre Les Nancy, France.
Stephen B WalshCentre for Nephrology, University College London, London, UK; and.
Jacques TeulonUnité Mixte de Recherche en Santé 1138, Team 3, Université Pierre et Marie Curie, Paris, France.
Anne BlanchardFaculté de Médecine, Université Paris Descartes, Paris, France.
Rosa Vargas-PoussouDepartment of Genetics and.
Sorbonne Université · FRAssistance Publique – Hôpitaux de Paris · FRAix-Marseille Université · FRCentre de Recherche en Acquisition et Traitement de l'Image pour la Santé · FRCentre Hospitalier du Pays d'Aix · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Sainte-Anne · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Besançon · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Tours · FRCHU Dijon Bourgogne · FRDélégation Paris 5 · FRHôpital Charles-Nicolle · FRHôpital de la Croix-Rousse · FRHôpital de la Timone · FR
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bartter syndrome type 3 is a clinically heterogeneous hereditary salt-losing tubulopathy caused by mutations of the chloride voltage-gated channel Kb gene (
Indexed as
AdolescentAdultBartter SyndromeChildChild, PreschoolFemaleGenetic Association StudiesHumansInfantMaleMutationRetrospective StudiesYoung AdultBartter-s syndromechronic kidney diseasehuman geneticsproteinuria
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