Disease: Hypokalemic alkalosis with hypercalcinuria
- A clinical and hereditary analysis of novel complex heterozygous <em>KCNJ1</em> mutation in a Bartter syndrome type Ⅱ patient
- A clinical and hereditary analysis of novel complex heterozygous KCNJ1 mutation in a Bartter syndrome type patient
- A nationwide retrospective study in Turkish children with nephrocalcinosis
- A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency
- A novel compound heterozygous KCNJ1 gene mutation presenting as late-onset Bartter syndrome: Case report
- A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH)(2) vitamin D levels
- A novel homozygous CLCNKB variant: An early presentation of classic Bartter syndrome in a neonate
- A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter's syndrome with 4 years follow-up
- A novel SLC12A1 gene mutation associated with hyperparathyroidism, hypercalcemia, nephrogenic diabetes insipidus, and nephrocalcinosis in four patients
- A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I
- A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis
- A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5
- A Rare Presentation of Adult-Onset Bartter Syndrome: A Case Report
- Accentuated hyperparathyroidism in type II Bartter syndrome
- Acquired Bartter-Like Phenotype
- Activating Calcium-Sensing Receptor Mutations: Prospects for Future Treatment with Calcilytics
- Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemia
- Anaesthetic management for hiatal hernia repair in a child with Bartter's syndrome: A case report
- Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in <em>SLC12A1 Gene</em>
- Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene
- Antenatal Bartter syndrome presenting as hyperparathyroidism with hypercalcemia and hypercalciuria: a case report and review
- Antenatal bartter syndrome: a review
- Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology
- Association of Amelogenesis Imperfecta and Bartter's Syndrome
- Association of Mutations in SLC12A1 Encoding the NKCC2 Cotransporter With Neonatal Primary Hyperparathyroidism
- Bartter syndrome in a female infant: A rare case report from Syria
- Bartter Syndrome Presenting as Arginine-Vasopressin Resistance: A Report of 2 Cases
- Bartter Syndrome Type 1 Due to Novel <em>SLC12A1</em> Mutations Associated With Pseudohypoparathyroidism Type II
- Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II
- Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes Insipidus
- Bartter syndrome: presentation in an extremely premature neonate
- Bartter-Gitelman syndromes
- Bartter-Like Syndrome as the Initial Presentation of Dent Disease 1: A Case Report
- Bartter-like Syndrome Induced By Tacrolimus in a Renal Transplanted Boy: A Case Report
- Bartter's syndrome: clinical findings, genetic causes and therapeutic approach
- Barttin Regulates the Subcellular Localization and Posttranslational Modification of Human Cl<sup>-</sup>/H<sup>+</sup> Antiporter ClC-5
- Calcium-sensing receptor: Role in health and disease
- Clinical and genetic analysis of Dent' s disease in 6 Chinese children with low molecular weight proteinuria
- Clinical and Genetic Spectrum of Bartter Syndrome Type 3
- Clinical Findings and Genetic Analysis of Nine Mexican Families with Bartter Syndrome
- Clinical profile and outcome of renal tubular disorders in children: A single center experience
- Comparison of Renal Stones and Nephrocalcinosis in Children: Findings From Two Tertiary Centers in Saudi Arabia
- Considerations about the molecular basis of some kidney tubule disorders in relation to inbreeding and population displacement
- Cystinosis presenting with findings of Bartter syndrome
- Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene
- Diseases associated with calcium-sensing receptor
- Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2
- Etiological Profile of Nephrocalcinosis in Children from Southern India
- Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis
- Functional activities of mutant calcium-sensing receptors determine clinical presentations in patients with autosomal dominant hypocalcemia
- Genetic and biochemical features of the monogenic hereditary urolithiasis
- Genetics of kidney stone disease
- Gitelman syndrome with normocalciuria - a case report
- Hypocalcemia as the Initial Presentation of Type 2 Bartter Syndrome: A Family Report
- HYPOKALEMIC METABOLIC ALKALOSIS - A REPORT OF SIX CASES
- HYPOKALEMIC METABOLIC ALKALOSIS – A REPORT OF SIX CASES
- Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome
- Identification of compound heterozygous KCNJ1 mutations (encoding ROMK) in a kindred with Bartter's syndrome and a functional analysis of their pathogenicity
- Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes
- Impaired phosphorylation of Na(+)-K(+)-2Cl(-) cotransporter by oxidative stress-responsive kinase-1 deficiency manifests hypotension and Bartter-like syndrome
- Inherited secondary nephrogenic diabetes insipidus: concentrating on humans
- Isolated nephrocalcinosis due to compound heterozygous mutations in renal outer medullary potassium channel
- Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and high parathyroid hormone levels mimicking primary hyperparathyroidism
- Late-onset Bartter syndrome type II
- Late-Onset Bartter's Syndrome Type II with End-Stage Renal Disease Due to a Novel Mutation in KCNJ1 Gene in an Indian Adult Male - A Case Report
- Living kidney donation from people at risk of nephrolithiasis, with a focus on the genetic forms
- Loop disorders: insights derived from defined genotypes
- Mechanisms and causes of hypomagnesemia
- Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis
- Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians
- Molecular pathophysiology of Bartter's and Gitelman's syndromes
- Monogenic urinary lithiasis in Tunisian children: 25 years' experience of a referral center
- mTOR-Activating Mutations in <em>RRAGD</em> Are Causative for Kidney Tubulopathy and Cardiomyopathy
- Nephrocalcinosis as adult presentation of Bartter syndrome type II
- Nephrocalcinosis in children
- Osteomalacia in a Case of Adult-Onset Bartter Syndrome
- Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1
- Physiology and pathophysiology of the calcium-sensing receptor in the kidney
- Polymyxin B-induced Bartter syndrome
- Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome
- Profile of renal diseases in Iraqi children: A single-center report
- Pseudo-Gitelman Syndrome Presenting with Hypokalemic Metabolic Alkalosis and Hypocalciuria
- Recurrent symptomatic hypocalcemia during rifampicin therapy for brucellosis
- Recurrent urinary tract infections in an infant with antenatal Bartter syndrome
- Renal function and linear growth of children with nephrocalcinosis: a retrospective single-center study
- Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome
- RenalTube: a network tool for clinical and genetic diagnosis of primary tubulopathies
- Research progress on renal calculus associate with inborn error of metabolism
- Review of childhood genetic nephrolithiasis and nephrocalcinosis
- Secondary hyperaldosteronism and medullary nephrocalcinosis caused by self-administered and uncontrolled laxative use in an adolescent patient
- Simultaneous Homozygous Mutations in <em>SLC12A3</em> and <em>CLCNKB</em> in an Inbred Chinese Pedigree
- Transient hyponatremia of prematurity caused by mild Bartter syndrome type II: a case report
- Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidus
- Type IV neonatal Bartter syndrome complicated with congenital chloride diarrhea
- Type-5 Bartter syndrome presenting with metabolic seizure in adulthood
- Unusual case of failure to thrive: Type III Bartter syndrome
- Unusual Complication of Multidrug Resistant Tuberculosis
- Urinary proteome in inherited nephrolithiasis
- WNK signalling pathways in blood pressure regulation
- Young Adults With Hereditary Tubular Diseases: Practical Aspects for Adult-Focused Colleagues