Summary: This case report describes a patient with MELAS syndrome (genetic multisystem disorder) treated with L-arginine therapy and corticosteroids.

Summary: Bartter syndrome and hypothyroidism masquerading cystinosis in a 3-year-old girl: rare manifestation of a rare disease.

Summary: Hypokalaemic quadriparesis with respiratory failure due to latent Sjogren syndrome.

Summary: Characterization of the clinical and genetic spectrum of autoimmune polyendocrine syndrome type 1 in Chinese case series.

Summary: Hypokalaemic paralysis as the initial clinical presentation of Sjogren's syndrome induced distal renal tubular acidosis.

Summary: Renal tubular distal acidosis: nephrocalcinosis as initial diagnosis.

Summary: Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis.

Summary: Renal tubular acidosis (RTA) and kidney stones: Diagnosis and management.

Summary: Medical management of urolithiasis.

Summary: Primary Sjögren's syndrome manifesting as sclerotic metabolic bone disease.

Summary: Biomarkers and Diagnostic Testing for Renal Disease in Sjogren's Syndrome.

Summary: This case report describes a 50-year-old HIV-positive male on tenofovir diagnosed with proximal renal tubular acidosis and fracture of left neck of femur four years after initiation of the drug.