• "Aldolase A" deficiency with syndrome of growth and developmental retardation, midfacial hypoplasia, hepatomegaly, and consanguineous parents
• A Manganese-independent Aldolase Enables Staphylococcus aureus To Resist Host-imposed Metal Starvation
• A new phenotype of aldolase a deficiency in a 14 year-old boy with epilepsy and rhabdomyolysis - case report
• A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency
• A thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemia
• Acute rhabdomyolysis and inflammation
• Aldolase A deficiency
• Aldolase A deficiency: Report of new cases and literature review
• Epidemiological aspects of hereditary fructose intolerance: A database study
• Estimation of hereditary fructose intolerance prevalence in the Chinese population
• Glycogen Storage Disease
• Glycogen Storage Disease
• Glycogen storage disease type XII; an ultra rare cause of hemolytic anemia and rhabdomyolysis: one new case report
• Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr)
• Hereditary myopathies associated with hematological abnormalities
• Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation
• Human aldolase A of a hemolytic anemia patient with Asp-128----Gly substitution: characteristics of an enzyme generated in E. coli transfected with the expression plasmid pHAAD128G
• Identification of a novel mutation in the <em>ALDOB</em> gene in hereditary fructose intolerance
• Isoquercitrin Upregulates Aldolase C Through Nrf2 to Ameliorate OGD/R-Induced Damage in SH-SY5Y Cells
• Molecular and clinical findings of Turkish patients with hereditary fructose intolerance
• Novel protein markers of androgen activity in humans: proteomic study of plasma from young chemically castrated men
• Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study
• RecQ dysfunction contributes to social and depressive-like behavior and affects aldolase activity in mice
• SIRT2 ablation inhibits glucose-stimulated insulin secretion through decreasing glycolytic flux