• "Self-Harming the Tubules" - A Rare Case of Renal Tubular Acidosis
• A case of Fanconi syndrome that developed following a year of consumption of a red yeast rice supplement
• A Case Report of Paralysis and Respiratory Difficulty in a Patient With a Recent History of Complicated Pregnancy - An Uncommon Expression of Distal Renal Tubular Acidosis
• A Conundrum of Severe Hypokalaemic Quadriparesis, Acute Kidney Injury, and Lung Involvement as the Initial Presentation of Catastrophic Primary Sjögren's Syndrome: Is it a New Entity? A Case Report
• A pH imbalance is linked to autophagic dysregulation of inner ear hair cells in Atp6v1ba-deficient zebrafish
• A Rare Presentation of Sarcoidosis in a Young Male With Acute Renal Failure: A Case Report and Literature Review
• A real-world disproportionality analysis of FDA adverse event reporting system events for ibuprofen
• A real-world disproportionality analysis of the FDA adverse event reporting system events for ibuprofen
• A review of renal tubular acidosis
• Acquired Fanconi syndrome in mixed cryoglobulinemia patients: a single-center case series
• Administration of bicarbonates through percutaneous gastrostomy with continuous nocturnal infusion in a patient with Kearns-Sayre disease: a life changing therapeutical paradigm
• Allogenic hematopoietic stem cell transplantation in an Iranian patient with osteopetrosis caused by carbonic anhydrase II deficiency: A case report
• Alteration of bone microarchitecture in hereditary distal RTA patients with SLC4A1 gene mutation: assessed by HR-pQCT
• An Interesting Case of Acquired Renal Fanconi Syndrome
• Analysis of risk factors and development of a nomogram prediction model for renal tubular acidosis in primary Sjogren syndrome patients
• Anatomy, Abdomen and Pelvis: Kidney Collecting Ducts
• Aromatic Hydrocarbon Toxicity: Benzene and Toluene
• Arterial Blood Gas
• Autoimmune Switch From Graves' Disease to Hashimoto's Thyroiditis With Coexisting Sjogren's Syndrome: A Case of Polyautoimmunity in a Young Woman
• Beyond Immunosuppression: The Intricate Relationship Between Tacrolimus and Microangiopathy
• Carbonic Anhydrase II Deficiency: Unusual Presentation of the Arabic Mutation. A Case Report
• Clinical and laboratory characteristics of salivary gland ultrasonography-positive patients with primary Sjögren's syndrome
• Clinical characteristics and genetic profile of children with WDR72-associated distal renal tubular acidosis: a nationwide experience
• Clinical manifestations and renal pathology of ethylene glycol
• Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome
• Comparison of clinical and immunological characteristics between primary Sjögren's syndrome patients with positive and negative anti-SSB antibody
• Comprehensive GC-MS Measurement of Amino Acids, Metabolites, and Malondialdehyde in Metformin-Associated Lactic Acidosis at Admission and during Renal Replacement Treatment
• Consenso mexicano de tirosinemia tipo 1
• Death by accidental intravenous administration of gasoline
• Demystifying normal-anion-gap metabolic acidosis: pathophysiology, aetiology, evaluation and diagnosis
• Diagnosis, management and outcomes of primary hypokalemic periodic paralysis during pregnancy
• Distal renal tubular acidosis as a rare complication of vesicoureteral reflux in children: a case report and literature review
• Effects of higher dietary acid load: a narrative review with special emphasis in children
• Eosinophilic cystitis-an obscure case of obstructive uropathy in infancy
• Etiology and Biochemical Profile of Rickets in Tertiary Care Centres in Eastern India: A Retrospective Cross-sectional Study
• Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21
• Extrarenal complications of cystinosis
• Failure to Thrive With Severe Hypokalemia Yields Cystinosis Diagnosis in a 19-Month-Old Female Child: A Case Report
• Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation
• Foxp1 is Required for Renal Intercalated Dell Differentiation and Acid-Base Regulation
• Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia
• Higher Renal Net Acid Excretion, but Not Higher Phosphate Excretion, during Childhood and Adolescence Associates with the Circulating Renal Tubular Injury Marker Interleukin-18 in Adulthood
• Hyperaldosteronism
• Hypernatremia Masking a Case of Primary Sjogren Syndrome-induced Distal Renal Tubular Acidosis
• Hyperphosphatemia
• Hypoaldosteronism due to a novel SEC61A1 variant successfully treated with fludrocortisone
• Hypocitraturia as a biomarker of renal tubular acidosis in patients with Sjogren's disease
• Hypokalemia Related to Distal Renal Tubular Acidosis as an Initial Presentation of Primary Sjogren's Syndrome
• Hypokalemic Paralysis Revealing Primary Sjogren's Syndrome: A Case Report
• Hypokalemic quadriplegia in Sjogren's syndrome: A case report
• Importance about use of high-throughput sequencing in pediatric: case report of a patient with Fanconi-Bickel syndrome
• Importance of genetic sequencing studies in managing chronic neonatal diarrhea: a case report of a novel variant in the glucose-galactose transporter SLC5A1
• In memoriam: Todd S. Ing, MD
• In memoriam: Todd S. Ing, MD, FACP
• Intracranial hypertension syndrome as an unusual manifestation of Sjögren's syndrome. Report of one case
• Intrarenal pH-Responsive Self-Assembly of Luminescent Gold Nanoparticles for Diagnosis of Early Kidney Injury
• Isolated short stature as the only presenting symptom of glycogen storage disease type 0a in a Chinese child: A case report
• Kidney involvement in Wilson's disease: a review of the literature
• Lessons learned from the real-world diagnosis and management of hereditary hypophosphatemic rickets
• Low potassium activation of proximal mTOR/AKT signaling is mediated by Kir4.2
• Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group
• Medullary nephrocalcinois and primary hyperaldosteronism - A rare and under recognised association
• Medullary Sponge Kidney
• Medullary Sponge Kidney and its Relationship with Primary Distal Renal Tubular Acidosis: Case Reports and a Comprehensive Genetics First Approach
• Medullary Sponge Kidney and Its Relationship with Primary Distal Renal Tubular Acidosis: Case Reports and a Comprehensive Genetics-First Approach
• Metabolic acidosis in chronic kidney disease: mere consequence or also culprit?
• Nephrolithiasis associated to Nephrocalcinosis is Primarily Composed of Carbonate Apatite
• Nephrolithiasis Associated with Nephrocalcinosis Is Primarily Composed of Carbonate Apatite
• Nephrology picture: metabolic acidosis with acute tubular injury-a noteworthy case
• Pediatric Renal Rickets at a Tertiary Center
• Prevalence and determinants of failure to thrive in children with vesico-ureteral reflux
• Primary Distal Renal Tubular Acidosis: Toward an Optimal Correction of Metabolic Acidosis
• Primary Distal Renal Tubular Acidosis: Towards an Optimal Correction of Metabolic Acidosis
• Primary Sjogren's syndrome presenting as hypokalaemic periodic paralysis and acute pancreatitis
• Pseudohypoaldosteronism and acquired renal aldosterone resistance with hyperkalemic type IV renal tubular acidosis in 2 cats
• Rare renal proximal tubular dysfunctions in primary biliary cholangitis
• Renal calcification in children with renal tubular acidosis: What a paediatrician should know
• Renal Tubular Acidosis
• Renal tubular acidosis in hereditary transthyretin amyloidosis (ATTRv)
• Renal Tubular Acidosis in the Neonate
• Review of childhood genetic nephrolithiasis and nephrocalcinosis
• Risk factors of primary Sjögren's syndrome combined with osteoporosis
• Secondary pseudohypoaldosteronism: a 15-year experience and a literature review
• Severe Electrolyte Abnormalities and Distal Renal Tubular Acidosis in the Setting of Apremilast Use for Psoriatic Arthritis: A Case Report
• Sex-specific Stone-forming Phenotype in Mice During Hypercalciuria/Urine Alkalinization
• SGLT2 Inhibitor Use for Treatment of Hypocitraturia in a Distal Renal Tubular Acidosis
• State of knowledge on ammonia handling by the kidney
• Systemic lupus erythematosus complicated with Fanconi syndrome: a case report and literature review
• Tenofovir-Associated Kidney Dysfunction and Bone Fracture: A Case Report and Literature Review
• The Atypical Presentation of Ifosfamide-Induced Renal Tubular Acidosis
• The Experience of Using Urinary Liver-Type Fatty Acid-Binding Protein for Follow-Up of Toluene Poisoning: A Case Report
• The impact of kidney stone disease on quality of life in high-risk stone formers
• The importance of arterial blood gas analysis as a systemic diagnosis approach in assessing and preventing chronic diseases, from emergency medicine to the daily practice
• Treatment of paediatric renal tubular acidosis with a prolonged-release alkali supplementation
• Type 1 Renal Tubular Acidosis in Wilson's Disease
• Unraveling the molecular landscape of kAE1: a narrative review
• Unusual presentation of Sjogren's syndrome
• Unusual presentation of Sjogren's syndrome during pregnancy: a case report
• Variables Associated With Hyperkalemic Renal Tubular Acidosis in Solid Organ Transplant Recipients
• When Two Syndromes Collide: Managing Fanconi and Refeeding Syndrome in a Single Patient