Disease: Hyperferritinemia- hereditary- with congenital cataracts
- 1-Year Incidence of Tuberculosis Infection and Disease Among Household Contacts of Rifampin- and Multidrug-Resistant Tuberculosis
- A case of iron deficiency anemia with extremely hyperferritinemia responds well to oral iron: the first identified hereditary hyperferritinemia cataract syndrome in China
- A child with hyperferritinemia: case report
- A new family with hereditary hyperferritinemia cataract syndrome
- A novel deletion in the iron-response element of the L-ferritin gene, causing hyperferritinaemia cataract syndrome
- A novel double nucleotide variant in the ferritin-L iron-responsive element in a Finnish patient with hereditary hyperferritinaemia-cataract syndrome
- A rare cause of hyperferritinemia without iron overload
- Age-dependent ocular phenotype in hereditary hyperferritinaemia cataract syndrome (HHCS)
- Analysis of a child with CLN1 neuronal ceroid lipofuscinosis in conjunct with Hereditary hyperferinemia cataract syndrome
- Aqueous humor ferritin in hereditary hyperferritinemia cataract syndrome
- Brazilian family with hyperferritinemia-cataract syndrome: case report
- Classification and diagnosis of iron overload
- Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome
- Family with marked hyperferritinemia as a result of hemochromatosis type 4 (ferroportin disease)
- Ferritin L-subunit gene mutation and hereditary hyperferritinaemia cataract syndrome (HHCS): a case report and literature review
- Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome
- Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome
- Ferroportin Q248H mutation, hyperferritinemia and atypical type 2 diabetes mellitus in South Kivu
- Frequent Mutation in the <em>FTL</em> Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G
- Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G
- FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family
- FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family
- FTL gene mutation and persistent hyperferritinemia without iron deficiency anemia after phlebotomy
- Functional characterization of a novel non-coding mutation "Ghent +49A > G" in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome
- Functional characterization of a novel non-coding mutation "Ghent +49A > G" in the iron-responsive element of L-ferritin causing hereditary hyperferritinaemia-cataract syndrome
- Genetic disorders affecting proteins of iron metabolism: clinical implications
- Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families
- Hematologic biomarkers in childhood cataracts
- Hepcidin levels in hereditary hyperferritinemia: Insights into the iron-sensing mechanism in hepatocytes
- Hereditary hyperferritinaemia cataract syndrome
- Hereditary hyperferritinaemia-cataract syndrome (HHCS) - an underestimated condition: ferritin light chain variant spectrum in German families
- Hereditary hyperferritinemia cataract syndrome
- Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia
- Hereditary hyperferritinemia cataract syndrome in four patients with mutations in the IRE of the FTL gene
- Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 families
- Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases
- Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a Swiss family
- Hereditary hyperferritinemia-cataract syndrome caused by a 29-base pair deletion in the iron responsive element of ferritin L-subunit gene
- Hereditary hyperferritinemia-cataract syndrome in two large multigenerational American families
- Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA
- Hereditary hyperferritinemia-cataract syndrome. Unusual differential diagnosis of unexplainable high levels of ferritin
- High level of ferritin light chain mRNA in lens
- Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype
- Hyperferritinaemia and macrophage activation in a patient with interstitial lung disease with clinically amyopathic DM
- Hyperferritinemia and inflammation
- Hyperferritinemia cataract syndrome
- Hyperferritinemia-cataract syndrome associated to the HFE gene mutation. Two new Spanish families and a new mutation (A37T: "Zaragoza")
- Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family
- Hyperferritinemia, ferropenia and metabolic syndrome in a patient with a new mutation of gene TFR2 and another in gene FTL. A family study
- Hyperferritinemic syndrome: Still's disease and catastrophic antiphospholipid syndrome triggered by fulminant Chikungunya infection: a case report of two patients
- Identification of the mutations associated with hereditary hyperferritinemia cataract syndrome and hemochromatosis in a Brazilian family
- Iron deficiency anaemia and cataracts in a patient with haemochromatosis
- Isolated hyperferritinemia in a healthy male infant: hereditary hyperferritinemia-cataract syndrome
- Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")
- New mutation in a Spanish family with hereditary hyperferritinemia-cataract syndrome
- Non-HFE hemochromatosis: pathophysiological and diagnostic aspects
- Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome
- Precision Medicine through Next-Generation Sequencing in Inherited Eye Diseases in a Korean Cohort
- Predictive factors of occult cystobiliary fistulas during conservative treatment of hepatic hydatid cyst: a prospective study
- Raised serum ferritin concentration in hereditary hyperferritinemia cataract syndrome is not a marker for iron overload
- Sequence analysis of exon 1 of the ferritin light chain (FTL) gene can reveal the rare disorder 'hereditary hyperferritinaemia without cataracts'
- Simultaneous presentation of hereditary hyperferritinaemia cataract syndrome and hereditary haemochromatosis
- Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin
- The hereditary hyperferritinemia-cataract syndrome: a family study
- The hyperferritinemic syndrome: macrophage activation syndrome, Still's disease, septic shock and catastrophic antiphospholipid syndrome