• "Every Cloud Has a Silver Lining": How Three Rare Diseases Defend Themselves from COVID-19 and What We Have Learnt from It
• A case of advanced breast cancer with Gitelman syndrome
• A case of pseudo-Bartter/Gitelman syndrome caused by long-term laxative abuse, leading to end-stage kidney disease
• A case report of Gitelman syndrome in children
• A missense variant in SLC12A3 gene enhances aberrant splicing causing Gitelman syndrome
• A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature
• A triple SLC12A3 heterozygous mutations in Gitelman syndrome with renal calculi
• Adult classic Bartter syndrome: a case report with 5-year follow-up and literature review
• Advanced chronic kidney disease with life-threatening hypokalemia due to undiagnosed Gitelman syndrome
• An unusual complication secondary to kanamycin use in a patient of multidrug-resistant pulmonary tuberculosis
• Anesthetic Considerations for Cesarean Delivery in a Parturient With Severe Gitelman Syndrome
• Angiotensin II, RAS Activation, and RAS Blockers in COVID-19: Unambiguous Evidence
• Bartter and Gitelman syndromes
• Bartter Syndrome
• Bartter Syndrome
• Bartter Syndrome-Related Variants Distribution: Brazilian Data and Its Comparison with Worldwide Cohorts
• Cardiac Arrest as the First Presentation of Gitelman Syndrome
• Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing
• Case report: Two novel compound heterozygous variant of SLC12A3 gene in a gitelman syndrome family and literature review
• Chemotherapy-induced tubulopathy: a case report series
• Clinical and genetic analysis of a case of Gitelman syndrome accompanied with Graves disease and adrenocortical adenoma: A case report
• Clinical and genetic analysis of a case of Gitelman syndrome with comorbid Graves disease and adrenocortical adenoma
• Clinical Course and Prognosis of Tubulopathies Characterized by Metabolic Alkalosis in Children
• Clinicopathological Features of Gitelman Syndrome with Proteinuria and Renal Dysfunction
• Diabetic ketoacidosis in a patient known with Gitelman syndrome
• Difficulties in the management of hypokalemia in a pregnant patient with Gitelman syndrome
• Electrolyte Disorders in Mitochondrial Cytopathies: A Systematic Review
• First Diagnosis of Gitelman Syndrome During Pregnancy in an Adolescent Female: A Case Report
• Genetic analysis of two patients with Gitelman syndrome
• Genetic diagnosis and treatment of hereditary renal tubular disease with hypokalemia and alkalosis
• Genotype-phenotype correlations in children with Gitelman syndrome
• Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3
• Gitelman Syndrome
• Gitelman Syndrome
• Gitelman syndrome - A new mutation in the SLC12A3 gene
• Gitelman Syndrome and Hypertension: A Case Report
• Gitelman syndrome and in vitro fertilization-embryo transfer: advancing preconception care in nephrology
• Gitelman syndrome and type 1 diabetes mellitus: An uncommon association
• Gitelman syndrome combined with diabetes mellitus: A case report and literature review
• Gitelman Syndrome Manifesting With Acute Hypokalemic Paralysis: A Case Report
• Gitelman Syndrome Presenting with Cerebellar Ataxia and Tetany
• Gitelman syndrome presenting with primary nocturnal enuresis: Causation or coincidence?
• Gitelman syndrome with Graves' disease leading to rhabdomyolysis: a case report and literature review
• Gitelman syndrome: A case report
• Gitelman Syndrome: A Case Report
• Gitelman's Syndrome in Pregnancy With Adverse Foetal Outcome: A Case Report
• Heart's Dangerous Symphony: Torsade De Pointes Unleashed by Gitelman Syndrome-Induced Hypomagnesemia
• HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
• Hyperaldosteronism
• Hypokalemic Periodic Paralysis Secondary to Medullary Sponge Kidney Complicated With Renal Tubular Acidosis
• Interpreting epigenetic causes of recurrent hypokalemia and seizures: Gitelman syndrome co-exist with pseudohypoparathyroidism type 1B
• Intriguing association between type 1 diabetes mellitus, Gitelman syndrome and Cacci-Ricci disease: Triad of rare diseases: A case report
• Joint manifestations revealing inborn metabolic diseases in adults: a narrative review
• Kinase Scaffold Cab39 Is Necessary for Phospho-Activation of the Thiazide-Sensitive NCC
• Knowing the meaning of the words we use: Gitelman's syndrome or Gitelman's disease?
• Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman Syndrome
• Long-Term Indomethacin Treatment in a Chinese Child with Gitelman Syndrome: Case Report and Literature Review on its Efficacy and Tolerance
• Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients
• Magnesium is crucial in renal-cardiovascular fibrosis but the Gitelman's syndrome paradox still awaits resolution
• Management of potassium-wasting syndrome in the antepartum, intrapartum and postpartum period
• METFORMIN-AND GLICLAZIDE-BASED DIABETES TREATMENT EXPERIENCE IN A PATIENT WITH GITELMAN SYNDROME
• Minigene splicing assays reveal new insights into exonic variants of the SLC12A3 gene in Gitelman syndrome
• Mitochondrial Dysfunction in Kidney Tubulopathies
• Molecular complexity analysis of the diagnosis of Gitelman syndrome in China
• Navigating the Multifaceted Intricacies of the Na⁺-Cl^- cotransporter, a Highly Regulated and Key Effector in the Control of Hydromineral Homeostasis
• Navigating the multifaceted intricacies of the Na⁺-Cl^- cotransporter, a highly regulated key effector in the control of hydromineral homeostasis
• Novel compound heterozygous mutation of <em>SLC12A3</em> in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review
• Novel compound heterozygous mutation of SLC12A3 in Gitelman syndrome co-existent with hyperthyroidism: A case report and literature review
• Novel compound heterozygous variants of <em>SLC12A3</em> gene in a Chinese patient with Gitelman syndrome: a case report
• Novel compound heterozygous variants of SLC12A3 gene in a Chinese patient with Gitelman syndrome: a case report
• Novel heterozygous mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome: A care-compliant case report
• Novel Intronic Mutations of the <em>SLC12A3</em> Gene in Patients with Gitelman Syndrome
• Novel Intronic Mutations of the SLC12A3 Gene in Patients with Gitelman Syndrome
• Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome
• Ocular manifestations of the genetic renal tubulopathies
• Oxidants and Cardiorenal Vascular Remodeling-Insights from Rare Genetic Tubulopathies: Bartter's and Gitelman's Syndromes
• Paradoxes in magnesium transport in type 1 Bartter's syndrome and Gitelman's syndrome: a modeling analysis
• Participant characteristics in the prevention of gestational diabetes as evidence for precision medicine: a systematic review and meta-analysis
• Pathophysiologic approach in genetic hypokalemia: An update
• Pathophysiological role of Na-Cl cotransporter in kidneys, blood pressure, and metabolism
• Pattern of hereditary renal tubular disorders in Egyptian children
• Pseudo-Bartter syndrome in an infant without obvious underlying conditions: A case report
• Pseudo-Gitelman Syndrome Presenting with Hypokalemic Metabolic Alkalosis and Hypocalciuria
• Quantitation of Renin Activity in Plasma Using Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
• R158Q and G212S, novel pathogenic compound heterozygous variants in SLC12A3 of Gitelman syndrome
• Recurrent Episodes of Hypokalaemia during Treatment with Inhaled Beta-2 Agonist Revealing Gitelman Syndrome, an Uncommon Clinical Entity
• Regulation of kidney on potassium balance and its clinical significance
• Spectrum of Disorders associated with Tetany
• Spectrum of variants in a large Chinese Gitelman syndrome cohort
• Structure and thiazide inhibition mechanism of the human Na-Cl cotransporter
• Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review
• Teplizumab and β-Cell Function in Newly Diagnosed Type 1 Diabetes
• The first compound heterozygous mutations in SLC12A3 and PDX1 genes: a unique presentation of Gitelman syndrome with distinct insulin resistance and familial diabetes insights
• The genetic spectrum of Gitelman(-like) syndromes
• The Impact of Gitelman Syndrome on Cardiovascular Disease: From Physiopathology to Clinical Management
• Tophaceous gout in a young man with Gitelman syndrome: a case report with an overview
• Total colectomy for poorly controlled hypokalaemia due to Gitelman syndrome
• Two Brothers from Macedonia with Gitelman Syndrome
• Using human urinary extracellular vesicles to study physiological and pathophysiological states and regulation of the sodium chloride cotransporter
• Young Adults With Hereditary Tubular Diseases: Practical Aspects for Adult-Focused Colleagues