• "Sweet death": Fructose as a metabolic toxin that targets the gut-liver axis
• A Case Study of a Rare Disease (Fructosemia) Diagnosed in a Patient with Abdominal Pain
• A Novel Frameshift Mutation of the ALDOB Gene in a Korean Girl Presenting with Recurrent Hepatitis Diagnosed as Hereditary Fructose Intolerance
• Activation of AMPD2 drives metabolic dysregulation and liver disease in mice with hereditary fructose intolerance
• Acute liver failure in neonates with undiagnosed hereditary fructose intolerance due to exposure from widely available infant formulas
• Acute liver failure related to inherited metabolic diseases in young children
• Adult hereditary fructose intolerance
• Aldolase-B knockout in mice phenocopies hereditary fructose intolerance in humans
• An Infant With Hereditary Fructose Intolerance and a Novel Presentation of Disseminated Intravascular Coagulopathy Following Pyloromyotomy
• Are heterozygous carriers for hereditary fructose intolerance predisposed to metabolic disturbances when exposed to fructose?
• Boric acid-functionalized silver nanoparticles as SERS substrate for sensitive and rapid detection of fructose in artificial urine
• Celiac Disease in Conjunction with Hereditary Fructose Intolerance as a Rare Cause of Liver Steatosis with Mild Hypertransaminasemia-A Case Report
• Characterization of a human induced pluripotent stem cell line (FDCHi015-A) derived from PBMCs of a patient harbouring ALDOB mutation
• Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases
• Clinical Practice Guidelines for the Diagnosis and Management of Hereditary Fructose Intolerance
• Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentation
• Correction: Vitamin C and folate status in hereditary fructose intolerance
• Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance
• Descriptive Analysis of Carrier and Affected Hereditary Fructose Intolerance in Women during Pregnancy
• Design of mobile and website health application devices for drug tolerability in hereditary fructose intolerance
• Development of tools to facilitate the diagnosis of hereditary fructose intolerance
• Effect of a high fructose diet on metabolic parameters in carriers for hereditary fructose intolerance
• Endogenous Fructose Production and Metabolism Drive Metabolic Dysregulation and Liver Disease in Mice with Hereditary Fructose Intolerance
• Epidemiological aspects of hereditary fructose intolerance: A database study
• Estimation of hereditary fructose intolerance prevalence in the Chinese population
• Evaluation of the effects of fructose on oxidative stress and inflammatory parameters in rat brain
• Evaluation of the In Vivo and In Vitro Effects of Fructose on Respiratory Chain Complexes in Tissues of Young Rats
• Fatty liver disease and hypertransaminasemia hiding the association of clinically silent Duchenne muscular dystrophy and hereditary fructose intolerance
• Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises
• Fructose-1-Phosphate Aldolase Deficiency
• Fructose-1-Phosphate Aldolase Deficiency
• Fructose-1,6-bisphosphatase deficiency: estimation of prevalence in the Chinese population and analysis of genotype-phenotype association
• Fructosuria and recurrent hypoglycemia in a patient with a novel c.1693T>A variant in the 3' untranslated region of the aldolase B gene
• Fruit-induced FPIES masquerading as hereditary fructose intolerance
• Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption
• Genetic disorder in carbohydrates metabolism: hereditary fructose intolerance associated with celiac disease
• Genomic analysis of lean individuals with NAFLD identifies monogenic disorders in a prospective cohort study
• Hereditary fructose intolerance
• Hereditary Fructose Intolerance
• Hereditary Fructose Intolerance
• Hereditary Fructose Intolerance Diagnosed in Adulthood
• Hereditary fructose intolerance in Brazilian patients
• Hereditary fructose intolerance mimicking a biochemical phenotype of mucolipidosis: A review of the literature of secondary causes of lysosomal enzyme activity elevation in serum
• Hereditary fructose intolerance: A comprehensive review
• Hereditary fructose intolerance: functional study of two novel ALDOB natural variants and characterization of a partial gene deletion
• Identification of a novel mutation in the <em>ALDOB</em> gene in hereditary fructose intolerance
• Identification of a novel mutation in the ALDOB gene in hereditary fructose intolerance
• Improving patient tolerability in immunoglobulin treatment: focus on stabilizer effects
• Inborn errors of carbohydrate metabolism
• Inborn Errors of Fructose Metabolism. What Can We Learn from Them?
• Inborn Errors of Metabolism with Hepatopathy: Metabolism Defects of Galactose, Fructose, and Tyrosine
• Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population
• Inherited Fanconi syndrome
• Integration of PCR-Sequencing Analysis with Multiplex Ligation-Dependent Probe Amplification for Diagnosis of Hereditary Fructose Intolerance
• Is liver steatosis diagnostic of non-alcoholic fatty liver disease in patients with hereditary fructose intolerance?
• Is medical nutrition therapy (MNT) the same for hereditary vs dietary fructose intolerance?
• Ketohexokinase C blockade ameliorates fructose-induced metabolic dysfunction in fructose-sensitive mice
• Ketohexokinase knockout mice, a model for essential fructosuria, exhibit altered fructose metabolism and are protected from diet-induced metabolic defects
• KHK inhibition for the treatment of hereditary fructose intolerance and nonalcoholic fatty liver disease: a double-edged sword
• Kidney and vascular function in adult patients with hereditary fructose intolerance
• Letter to the editor concerning the article 'Safety of vaccines administration in hereditary fructose intolerance'
• Liver adenomatosis and NAFLD developed in the context of hereditary fructose intolerance
• Medical management of chronic liver diseases in children (part I): focus on curable or potentially curable diseases
• Metabolic disorders of the liver.Part 2: glycogen storage diseases, hereditary fructose intolerance, galactosemia and hepatic porphyrias
• Molecular and clinical findings of Turkish patients with hereditary fructose intolerance
• Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India
• Mutations in the promoter region of the aldolase B gene that cause hereditary fructose intolerance
• Myths and Facts about Food Intolerance: A Narrative Review
• Neonatal Hereditary Fructose Intolerance: Diagnostic Misconceptions and the Role of Genomic Sequencing
• Neutrotoxic effects of fructose administration in rat brain: implications for fructosemia
• Non responsive celiac disease due to coexisting hereditary fructose intolerance
• Non-alcoholic fatty liver in hereditary fructose intolerance
• Patients With Aldolase B Deficiency Are Characterized by Increased Intrahepatic Triglyceride Content
• Pitfalls in the Diagnosis of Hereditary Fructose Intolerance
• Prevalence estimation for monogenic autosomal recessive diseases using population-based genetic data
• Quality of life of adult patients with hereditary fructose intolerance
• Rare causes of hypoglycemia in adults
• Rare monogenic causes of steatotic liver disease masquerading as MASLD
• Real-time tissue elastography (RTE) for noninvasive evaluation of fibrosis in liver diseases in children in comparison to liver biopsy
• Recent advances in the pathogenesis of hereditary fructose intolerance: implications for its treatment and the understanding of fructose-induced non-alcoholic fatty liver disease
• Relapsing Acute Axonal Neuropathy in Hereditary Fructose Intolerance
• Reply letter to "safety of SARS-Cov-2 vaccines administration for adult patients with hereditary fructose intolerance"
• Reply letter to the editor concerning the article 'Safety of Sars-Cov-2 vaccines administration for adult patients with hereditary fructose intolerance'
• Reply-Letter to the Editor-Is liver steatosis diagnostic of non-alcoholic fatty liver disease in patients with hereditary fructose intolerance?
• Safety of Sars-Cov-2 vaccines administration for adult patients with hereditary fructose intolerance
• Safety of vaccines administration in hereditary fructose intolerance
• Secondary disorders of glycosylation in inborn errors of fructose metabolism
• Social and health care needs in patients with hereditary fructose intolerance in Spain
• Stabilization of the predominant disease-causing aldolase variant (A149P) with zwitterionic osmolytes
• Sweet ending: When genetics prevent a dramatic CDG diagnostic mistake
• Synergistic use of glycomics and single-molecule molecular inversion probes for identification of congenital disorders of glycosylation type-1
• Tenofovir as a cause of acquired fanconi's syndrome
• The biochemical basis of hereditary fructose intolerance
• Transferrin isoelectric focusing and plasma lysosomal enzyme activities in the diagnosis and follow-up of hereditary fructose intolerance
• Transferrin isoelectric focusing for the investigation of congenital disorders of glycosylation: analysis of a ten-year experience in a Brazilian center
• Transferrin Isoforms, Old but New Biomarkers in Hereditary Fructose Intolerance
• Utilization of Positive and Negative Controls to Examine Comorbid Associations in Observational Database Studies
• Vaccination strategies for people living with inborn errors of metabolism in Brazil
• Vitamin C and folate status in hereditary fructose intolerance
• When Long-Lasting Food Selectivity Leads to an Unusual Genetic Diagnosis: A Case Report