• A case of acute kidney injury and Fanconi syndrome while taking multiple supplements, including Red Yeast Rice Cholesterol Help^®
• A case of hyperlysinemia identified by urine newborn screening
• A case of ifosfamide-induced acute kidney injury, Fanconi syndrome, and nephrogenic diabetes insipidus
• A Summary of Current Guidelines and Future Directions for Medical Management and Monitoring of Patients with Cystinuria
• A Unique Observation of a Patient with Vulto-van Silfhout-de Vries Syndrome
• Aminoaciduria and metabolic dysregulation during diabetic ketoacidosis: Results from the diabetic kidney alarm (DKA) study
• An Interesting Case of Acquired Renal Fanconi Syndrome
• Aspartic Acid in Health and Disease
• Band-shaped keratopathy in <em>HNF4A</em>-related Fanconi syndrome: a case report and review of the literature
• Clinical Features and Genetic Sequencing of Children with Fanconi-Bickel Syndrome
• Distal renal tubular acidosis as presenting manifestation of Wilson disease in a 11-year-old girl
• Excretion of excess nitrogen and increased survival by loss of SLC6A19 in a mouse model of ornithine transcarbamylase deficiency
• Extrarenal complications of cystinosis
• Familial Renal Glucosuria Presenting as Paroxysmal Glucosuria and Hypercalciuria Due to a Novel <em>SLC5A2</em> Heterozygous Variant
• Fanconi syndrome in a patient receiving pre-exposure prophylaxis for HIV infection: case report
• Fulminant Neonatal Liver Failure in MPV 17-Related Mitochondrial DNA Depletion Syndrome
• Genetic and clinical characterization of familial renal glucosuria
• Hartnup Disease
• Hartnup Disease
• Hydrocephalus presented as the prominent symptom of severe 5,10-methylenetetrahydrofolate reductase deficiency in an infant: A case report
• Hypokalemic Paralysis and Hypocalcemic Tetany: Paradoxical Duality in a Case of Sjogren's Syndrome
• Identification of two novel variants of BCS1L gene in a patient with classical GRACILE syndrome
• Lysinuric Protein Intolerance and Its Nutritional and Multisystemic Challenges in Pregnancy: A Case Report and Literature Review
• Lysinuric protein intolerance caused by a homozygous <em>SLC7A7</em> deletion and presented with hyperferritinemia and osteoporosis in two siblings
• Misdiagnosis and Mistreatment of a Rare Case of Intracranial Oncogenic Osteomalacia with an Altered Amino Acid Profile
• Outcome of Acquired Fanconi Syndrome Associated with Ingestion of Jerky Treats in 30 Dogs
• Pediatric metanephric adenoma with Fanconi-Bickel syndrome: a case report and review of literature
• Rare renal proximal tubular dysfunctions in primary biliary cholangitis
• Urinary angiotensin-converting enzyme 2 and metabolomics in COVID-19-mediated kidney injury
• When Two Syndromes Collide: Managing Fanconi and Refeeding Syndrome in a Single Patient