Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders
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Title
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders
Authors
Keywords
Bartter syndrome, hypokalemic metabolic alkalosis, inherited hypokalemia, salt-losing tubulopathy
Journal
KIDNEY INTERNATIONAL
Volume 99, Issue 2, Pages 324-335
Publisher
Elsevier BV
Online
2021-01-25
DOI
10.1016/j.kint.2020.10.035
References
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Note: Only part of the references are listed.- Markers of potassium homeostasis in salt losing tubulopathies- associations with hyperaldosteronism and hypomagnesemia
- (2020) Michael Eder et al. BMC Nephrology
- High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults
- (2019) Marguerite Hureaux et al. KIDNEY INTERNATIONAL
- Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies
- (2018) Emma J. Ashton et al. KIDNEY INTERNATIONAL
- Hydrochlorothiazide Test as a Tool in the Diagnosis of Gitelman Syndrome in Chinese Patients
- (2018) Xiaoyan Peng et al. Frontiers in Endocrinology
- Clinical and Genetic Spectrum of Bartter Syndrome Type 3
- (2017) Elsa Seys et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Salt-Losing Tubulopathies in Children: What’s New, What’s Controversial?
- (2017) Robert Kleta et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
- (2017) Anne Blanchard et al. KIDNEY INTERNATIONAL
- Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents
- (2017) Joseph T. Flynn et al. PEDIATRICS
- Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome
- (2017) Alejandro García Castaño et al. PLoS One
- New guideline for perioperative management of people with inherited salt-wasting alkaloses
- (2016) H Gallagher et al. BRITISH JOURNAL OF ANAESTHESIA
- Renal apnoea: extreme disturbance of homoeostasis in a child with Bartter syndrome type IV
- (2016) Lucy Anne Plumb et al. LANCET
- Polyhydramnios, Transient Antenatal Bartter’s Syndrome, andMAGED2Mutations
- (2016) Kamel Laghmani et al. NEW ENGLAND JOURNAL OF MEDICINE
- Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases
- (2015) Bichr Allaf et al. PRENATAL DIAGNOSIS
- Treatment of Bartter syndrome. Unsolved issue
- (2014) Carla Lessa Pena Nascimento et al. Jornal de Pediatria
- Full term; an artificial concept
- (2012) Neil Marlow Archives of Disease in Childhood-Fetal and Neonatal Edition
- Bartter syndrome and growth hormone deficiency: three cases
- (2012) Mithat Buyukcelik et al. PEDIATRIC NEPHROLOGY
- Antenatal Bartter syndrome: a rare cause of unexplained severe polyhydramnios
- (2011) Y R Bhat et al. ANNALS OF TROPICAL PAEDIATRICS
- Genetic basis of Bartter syndrome in Korea
- (2011) B. H. Lee et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Does hypokalaemia cause nephropathy? an observational study of renal function in patients with Bartter or Gitelman syndrome
- (2011) S. B. Walsh et al. QJM-AN INTERNATIONAL JOURNAL OF MEDICINE
- A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis
- (2010) Ipek Akil et al. Clinical and Experimental Nephrology
- ANTENATAL BARTTER SYNDROME: Analysis of Two Cases with Placental Findings
- (2010) Banu Dane et al. Fetal and Pediatric Pathology
- The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies
- (2010) Kandai Nozu et al. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Long-term follow-up of patients with Bartter syndrome type I and II
- (2010) E. Puricelli et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases
- (2010) D. Bockenhauer et al. NEPHRON PHYSIOLOGY
- Cardiac arrhythmias and rhabdomyolysis in Bartter–Gitelman patients
- (2010) Cinzia Cortesi et al. PEDIATRIC NEPHROLOGY
- Gestational Age at Delivery and Special Educational Need: Retrospective Cohort Study of 407,503 Schoolchildren
- (2010) Daniel F. MacKay et al. PLOS MEDICINE
- Review article: the clinical management of congenital chloride diarrhoea
- (2009) S. WEDENOJA et al. ALIMENTARY PHARMACOLOGY & THERAPEUTICS
- Bartter’s Syndrome in Pregnancy: Review of Potassium Homeostasis in Gestation
- (2009) Ashar Luqman et al. AMERICAN JOURNAL OF THE MEDICAL SCIENCES
- Hypokalemic rhabdomyolysis in congenital tubular disorders: a case series and a systematic review
- (2009) Rodo O. von Vigier et al. PEDIATRIC NEPHROLOGY
- Longitudinal growth in chronic hypokalemic disorders
- (2009) Helena Gil-Peña et al. PEDIATRIC NEPHROLOGY
- Myocardial perfusion defects in Bartter and Gitelman syndromes
- (2008) R. Scognamiglio et al. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
- Phenotype–genotype correlation in antenatal and neonatal variants of Bartter syndrome
- (2008) Karine Brochard et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Antenatal Bartter's syndrome: why is this not a lethal condition?
- (2008) D. Bockenhauer et al. QJM-AN INTERNATIONAL JOURNAL OF MEDICINE
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