• A Case of Diabetes Mellitus Type MODY5 as a feature of 17q12 Deletion Syndrome
• A case of digenic maturity onset diabetes of the young with heterozygous variants in both HNF1Α and HNF1Β genes
• A case of familial recurrent 17q12 microdeletion syndrome presenting with severe diabetic ketoacidosis
• A Case of Milk-Alkali Syndrome Caused by Diuretic-Induced Alkalosis and Polypharmacy
• A presentation of adenovirus with hypokalemia and rhabdomyolysis in pregnancy
• A prospective observational study to identify the effectiveness of intravenous magnesium replacement in an intensive care setting
• A Rare Case of Patiromer Induced Hypercalcemia
• A retrospective evaluation of furosemide and mannitol for prevention of cisplatin-induced nephrotoxicity
• A Study of Hypomagnesemia in Patients Admitted to the ICU
• Acute kidney injury during cisplatin therapy and associations with kidney outcomes 2 to 6 months post-cisplatin in children: a multi-centre, prospective observational study
• Adverse Effects Associated with Long-Term Use of Proton Pump Inhibitors
• AGA Clinical Practice Update on Diagnosis and Management of Acute Hepatic Porphyrias: Expert Review
• Association between hypomagnesemia and mortality among dialysis patients: a systematic review and meta-analysis
• Associations between the serum magnesium and all-cause or cardiovascular mortality in chronic kidney disease and end-stage renal disease patients: A meta-analysis
• Case Report: CNNM2 Mutations Cause Damaged Brain Development and Intractable Epilepsy in a Patient Without Hypomagnesemia
• Case report: extreme coronary calcifications and hypomagnesemia in a patient with a 17q12 deletion involving HNF1B
• Childhood nephrolithiasis and nephrocalcinosis caused by metabolic diseases and renal tubulopathy: A retrospective study from 2 tertiary centers
• Clinical and genetic approach to renal hypomagnesemia
• Clinical and genetic features of Kenny-Caffey syndrome type 2 with multiple electrolyte disturbances: A case report
• Comparison of Renal Stones and Nephrocalcinosis in Children: Findings From Two Tertiary Centers in Saudi Arabia
• Congenital macular scars in siblings from CLDN19 mutations
• Data of atrial arrhythmias in hospitalized COVID-19 and influenza patients
• Derivation and validation of a model to predict acute kidney injury following cardiac surgery in patients with normal renal function
• Diagnostic Dilemma in an Adolescent Girl with an Eating Disorder, Intellectual Disability, and Hypomagnesemia
• Differential localization patterns of claudin 10, 16, and 19 in human, mouse, and rat renal tubular epithelia
• Diseases caused by mutations in the Na⁺/K⁺ pump α1 gene <em>ATP1A1</em>
• Effect of Dapagliflozin and Magnesium Supplementation on Renal Magnesium Handling and Magnesium Homeostasis in Metabolic Syndrome
• Effect of proton pump inhibitors on the development of hypomagnesemia induced by panitumumab
• Electrolyte Abnormalities Associated With the Use of Atezolizumab - A Systematic Review
• Electrolyte Imbalance in Anti-LGI1 Encephalitis: It Is Not All in Your Head
• Experience with the potassium binder patiromer in hyperkalaemia management in heart failure patients in real life
• Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features
• Feasibility of long-term continuous subcutaneous magnesium supplementation in a patient with irreversible magnesium wasting due to cisplatin
• Furosemide rescues hypercalciuria in familial hypomagnesaemia with hypercalciuria and nephrocalcinosis model
• Gene-nutrient interactions that impact magnesium homeostasis increase risk for neural tube defects in mice exposed to dolutegravir
• Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability
• Gitelman syndrome presenting with cerebellar ataxia: a case report
• Gitelman syndrome with a novel frameshift variant in SLC12A3 gene accompanied by chronic kidney disease and type 2 diabetes mellitus
• Gitelman syndrome: A case report
• Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA
• HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
• HNF1B-MODY Masquerading as Type 1 Diabetes: A Pitfall in the Etiological Diagnosis of Diabetes
• Home Subcutaneous Magnesium Infusion in Refractory Hypomagnesemia: A Case Report
• Hypomagnesaemia in kidney transplantation
• Hypomagnesemia
• Hypomagnesemia as First Clinical Manifestation of ADTKD-HNF1B: A Case Series and Literature Review
• Hypomagnesemia due to two novel TRPM6 mutations
• Hypomagnesemia in the Cancer Patient
• Hypomagnesemia Is Associated with the Acute Kidney Injury in Traumatic Brain Injury Patients: A Pilot Study
• Iatrogenic Hypermagnesemia in a Patient With Preeclampsia Caused by Misinterpretation of the Magnesium Reporting Unit Following Magnesium Sulfate Administration
• Impact of Post-Transplantation Hypomagnesemia on Long-Term Graft and Patient Survival after Transplantation
• Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the <em>HNF1B</em> gene
• Inappropriate Use of Proton Pump Inhibitor Among Elderly Patients in British Columbia: What are the Long-term Adverse Events?
• Intestinal hypomagnesemia in an Iranian patient with a novel TRPM6 variant: a case report and review of the literature
• Magnesium Absorption in Intestinal Cells: Evidence of Cross-Talk between EGF and TRPM6 and Novel Implications for Cetuximab Therapy
• Magnesium Metabolism in Chronic Alcohol-Use Disorder: Meta-Analysis and Systematic Review
• Magnesium supplementation: A consideration in dialysis patients
• Maturity-onset diabetes of the young type 5, presenting as diabetic ketoacidosis with alkalemia: A report of a case
• Novel <em>CNNM2</em> Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure
• Novel compound heterozygous variants of <em>SLC12A3</em> gene in a Chinese patient with Gitelman syndrome: a case report
• Pathophysiologic approach in genetic hypokalemia: An update
• Physiology of a Forgotten Electrolyte-Magnesium Disorders
• Preoperative Ionized Magnesium Levels and Risk of Acute Kidney Injury After Cardiac Surgery
• Primary renal magnesium wasting: an unusual clinical picture of exercise-induced symptoms
• Protective Effect of Curcumin against Sodium Salicylate-Induced Oxidative Kidney Damage, Nuclear Factor-Kappa Dysregulation, and Apoptotic Consequences in Rats
• Proteinuria-associated renal magnesium wasting leads to hypomagnesemia: a common electrolyte abnormality in chronic kidney disease
• Proton Pump Inhibitor and Tacrolimus Uses are Associated With Hypomagnesemia in Connective Tissue Disease: a Potential Link With Renal Dysfunction and Recurrent Infection
• Proton-pump inhibitor use amongst patients with severe hypomagnesemia
• Reactive Oxygen Species Downregulate Transient Receptor Potential Melastatin 6 Expression Mediated by the Elevation of miR-24-3p in Renal Tubular Epithelial Cells
• Regional Citrate Anticoagulation during Double-Filtration Plasmapheresis in Kidney Transplant Recipients: A Single-Center Retrospective Cohort Study
• Regional citrate anticoagulation vs systemic heparin anticoagulation for double-filtration plasmapheresis
• Relationship between Proton Pump Inhibitors and Adverse Effects in Hemodialysis Patients: A Systematic Review and Meta-Analysis
• Relationship between renal dysfunction and electrolyte abnormalities in hematopoietic stem cell transplant patients treated with foscarnet
• Research progress on renal calculus associate with inborn error of metabolism
• Retrospective study of factors associated with progression and remission/regression of diabetic kidney disease-hypomagnesemia was associated with progression and elevated serum alanine aminotransferase levels were associated with remission or regression
• RRAGD-Associated Autosomal Dominant Kidney Hypomagnesemia with Cardiomyopathy: A Review on the Clinical Manifestations and Therapeutic Options
• Safety Assessment on Serious Adverse Events of Targeted Therapeutic Agents Prescribed for RAS Wild-Type Metastatic Colorectal Cancer: Systematic Review and Network Meta-Analysis
• Serum lipid peroxides and magnesium levels following three months of treatment with pioglitazone in patients with type-2 diabetes mellitus
• Serum magnesium in diabetic retinopathy: the association needs investigation
• Serum magnesium level as a predictor of acute kidney injury in patients with acute pancreatitis
• SGLT2 Inhibitors in Management of Severe Hypomagnesemia in Patients Without Diabetes: A Report of 4 Cases
• Single-dose rATG induction at renal transplantation: superior renal function and glucoregulation with less hypomagnesemia
• Sodium-Glucose Cotransporter 2 Inhibitors and Management of Refractory Hypomagnesemia Without Overt Urinary Magnesium Wasting: A Report of 2 Cases
• Subcutaneous Fat Necrosis of the Newborn
• The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing
• The Clinical Characteristics and Gene Mutations of Maturity-Onset Diabetes of the Young Type 5 in Sixty-One Patients
• The Clinical Characteristics of Electrolyte Disturbance in Patients with Moderate and Severe Traumatic Brain Injury Who Underwent Craniotomy and Its Influence on Prognosis
• The emerging role of magnesium in CKD
• The emerging roles and therapeutic potential of cyclin M/CorC family of Mg²⁺ transporters
• The importance of hypophosphatemia in the clinical management of primary hyperparathyroidism
• The Use of N-of-1 Trials to Individualize Treatment in Patients With Renal Magnesium Wasting
• Thiazide Responsiveness Testing in Patients With Renal Magnesium Wasting and Correlation With Genetic Analysis: A Diagnostic Test Study
• Transcription factor HNF1β controls a transcriptional network regulating kidney cell structure and tight junction integrity
• TRough versus AUC Monitoring of cyclosporine: A randomized comparison of adverse drug reactions in adult allogeneic stem cell recipients (TRAM study)
• TRPM7 deficiency exacerbates cardiovascular and renal damage induced by aldosterone-salt
• Tubular calcium, magnesium, and phosphate excretion during therapeutic hypothermia for neonatal hypoxic-ischemic encephalopathy: A prospective study
• Two Brothers from Macedonia with Gitelman Syndrome
• Type 2 diabetes control and complications and their relation to serum magnesium level
• Urinary Magnesium in the Evaluation of Hypomagnesemia
• Vestibular Disorders after Kidney Transplantation: Focus on the Pathophysiological Mechanisms Underlying the Vertical Nystagmus Associated with Tacrolimus-Related Hypomagnesamia