Disease: Gitelman syndrome
- "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 Gitelman Syndrome with Hypercalcemia Secondary to Primary Hyperparathyroidism
- A case of Gitelman syndrome with membranous nephropathy
- 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 novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature
- A novel mutation of <em>SLC12A3</em> gene causing Gitelman syndrome
- A novel mutation of SLC12A3 gene causing Gitelman syndrome
- 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
- 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
- Concurrent Gitelman Syndrome-like Tubulopathy and Grave's Disease
- Detecting pathogenic deep intronic variants in Gitelman syndrome
- 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
- 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 and Bartter's Syndromes: From Genetics to the Molecular Basis of Hypertension and More
- 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
- 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
- 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
- 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
- Multiple molecular mechanisms are involved in the activation of the kidney sodium-chloride cotransporter by hypokalemia
- Na-Cl Co-transporter (NCC) gene inactivation is associated with improved bone microstructure
- Navigating the Multifaceted Intricacies of the Na<sup>+</sup>-Cl<sup>-</sup> cotransporter, a Highly Regulated and 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
- 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
- Pattern of hereditary renal tubular disorders in Egyptian children
- Potassium and Magnesium in Breast Milk of a Woman With Gitelman Syndrome
- 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 Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing
- 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
- 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