• A complicated case of whole-lung lavage: a case report
• A complication of lysinuric protein intolerance: Intermittent haemophagocytic lymphohistiocytosis
• A novel variant in a Chinese boy with lysinuric protein intolerance: A case report and literature review
• A surprising cause of proteinuria: Answers
• Children with lysinuric protein intolerance: Experience from a lower middle income country
• Clinicopathologic features of non-lupus membranous nephropathy in a pediatric population
• Delayed skeletal development and IGF-1 deficiency in a mouse model of lysinuric protein intolerance
• Digital clubbing without hypoxia for lysinuric protein intolerance
• Enteral nutrition support for lysinuric protein intolerance: a case report and literature review
• Familial hemophagocytic lymphohistiocytosis syndrome due to lysinuric protein intolerance: a patient with a novel compound heterozygous pathogenic variant in SLC7A7
• Hemophagocytic Lymphohistiocytosis in Lysinuric Protein Intolerance
• Improving a Rare Metabolic Disorder Through Kidney Transplantation: A Case Report of a Patient With Lysinuric Protein Intolerance
• Inborn errors of amino acid metabolism - from underlying pathophysiology to therapeutic advances
• Lactulose: A treatment for hyperammonemia in a lysinuric protein-intolerant patient with dynamic blood amino acid concentrations
• 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
• Lysinuric protein intolerance caused by a homozygous SLC7A7 deletion and presented with hyperferritinemia and osteoporosis in two siblings
• Lysinuric protein intolerance exhibiting renal tubular acidosis/Fanconi syndrome in a Japanese woman
• Lysinuric protein intolerance presenting as pancytopenia and splenomegaly mimicking acute leukaemia: a case report
• Lysinuric protein intolerance with novel mutations in solute carrier family 7A member 7 in a Chinese family
• Membranoproliferative glomerulonephritis in a patient with lysinuric protein intolerance: lesson for the clinical nephrologist
• Neurological and endocrinological involvement in neonatal lupus erythematosus: a retrospective study at a tertiary hospital in Eastern China
• Plasma calprotectin is extremely high in patients with lysinuric protein intolerance
• Postnatal outcome of children with antenatal colonic hyperechogenicity
• Pulmonary phenotypes of inborn errors of metabolism
• Pulmonary proteinosis and secondary hemophagocytic syndrome in a patient with lysinuric protein intolerance
• Rare diseases presenting with hemophagocytic lymphohistiocytosis
• Reversal of SLE and hemophagocytic lymphohistiocytosis caused by lysinuric protein intolerance through allogeneic hematopoietic stem cell transplantation
• The diagnostic challenge of mild citrulline elevation at newborn screening
• The Great Masquerade: Varying Manifestations of Lysinuric Protein Intolerance
• TTCT 1471 mutation in lysnuric protein intolerance: Clinical features of a Tunisian paediatric series
• Whole lung lavage and GM-CSF use for pulmonary alveolar proteinosis in an infant with lysinuric protein intolerance: a case report