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Quoted phrase not found in phrase index: "Hereditary hyperferritinemia with congenital cataracts"
Page 1
Hyperferritinemia and inflammation.
Kernan KF, Carcillo JA. Kernan KF, et al. Int Immunol. 2017 Nov 1;29(9):401-409. doi: 10.1093/intimm/dxx031. Int Immunol. 2017. PMID: 28541437 Free PMC article. Review.
There is a clear need for further investigation of the role of ferritin in uncontrolled inflammatory conditions both as a biomarker and mediator of disease because its occurrence identifies patients with high mortality risk and its resolution predicts their improved surviv …
There is a clear need for further investigation of the role of ferritin in uncontrolled inflammatory conditions both as a biomarker and medi …
The hyperferritinemic syndrome: macrophage activation syndrome, Still's disease, septic shock and catastrophic antiphospholipid syndrome.
Rosário C, Zandman-Goddard G, Meyron-Holtz EG, D'Cruz DP, Shoenfeld Y. Rosário C, et al. BMC Med. 2013 Aug 22;11:185. doi: 10.1186/1741-7015-11-185. BMC Med. 2013. PMID: 23968282 Free PMC article. Review.
Ferritin is known to be a pro-inflammatory mediator inducing expression of pro-inflammatory molecules, yet it has opposing actions as a pro-inflammatory and as an immunosuppressant. We propose that the exceptionally high ferritin levels observed in these uncommon clinical …
Ferritin is known to be a pro-inflammatory mediator inducing expression of pro-inflammatory molecules, yet it has opposing actions as a pro- …
Hereditary hyperferritinemia-cataract syndrome in two large multigenerational American families.
Shekunov J, de Groen PC, Lindor NM, Klee GG, Aleff RA, Wieben ED, Mohney BG. Shekunov J, et al. J AAPOS. 2011 Aug;15(4):356-61. doi: 10.1016/j.jaapos.2011.03.020. J AAPOS. 2011. PMID: 21907119
The purpose of this study is to describe the genotypic and phenotypic manifestations of HHCS observed in 2 large sets of unrelated American families. METHODS: Forty-five patients were recruited from 2 unrelated families. ...
The purpose of this study is to describe the genotypic and phenotypic manifestations of HHCS observed in 2 large sets of unrelated Am …
Ferritin light chain gene mutation in a large Australian family with hereditary hyperferritinemia-cataract syndrome.
Yazar S, Franchina M, Craig JE, Burdon KP, Mackey DA. Yazar S, et al. Ophthalmic Genet. 2017 Mar-Apr;38(2):171-174. doi: 10.3109/13816810.2016.1164195. Epub 2016 Apr 20. Ophthalmic Genet. 2017. PMID: 27096259 Free article.
.-167 C>T) was identified in the proband and five affected family members (logarithm of the odds score [Z] = 3.61, recombination distance [teta = 0]). All affected individuals had previously been found to have high ferritin levels and early onset cataracts. ...
.-167 C>T) was identified in the proband and five affected family members (logarithm of the odds score [Z] = 3.61, recombination d …
Frequent Mutation in the FTL Gene Causing Hyperferritinemia Cataract Syndrome in Turkish Population Is c.-160A>G.
Balta B, Erdoğan M, Kiraz A, Korkmaz S, Ağadayı A. Balta B, et al. Turk J Haematol. 2019 Feb 7;36(1):25-28. doi: 10.4274/tjh.galenos.2018.2018.0194. Epub 2018 Nov 6. Turk J Haematol. 2019. PMID: 30401656 Free PMC article.
CONCLUSION: In the Turkish population, the prevalence of HFCS is about 1/100,000 and the commonly observed mutation is c.-160A>G mutation....
CONCLUSION: In the Turkish population, the prevalence of HFCS is about 1/100,000 and the commonly observed mutation is c.-160A>G m …
Predictive factors of occult cystobiliary fistulas during conservative treatment of hepatic hydatid cyst: a prospective study.
Trigui A, Fendri S, Akrout A, Trabelsi J, Daoud R, Saumtally MS, Ketata S, Baklouti S, Boujelbene W, Mzali R, Dziri C, Rejab H, Boujelbene S. Trigui A, et al. J Gastrointest Surg. 2024 Feb;28(2):108-114. doi: 10.1016/j.gassur.2023.11.011. Epub 2024 Feb 5. J Gastrointest Surg. 2024. PMID: 38445931
In a bivariate study, absence of mass and abdominal pain on palpation, hemoglobin level >11.55 g/dL, negative hydatid serology, cyst size, absence of calcifications, vascular compression, existence of a single cyst, and localization at segment VIII were predictive facto …
In a bivariate study, absence of mass and abdominal pain on palpation, hemoglobin level >11.55 g/dL, negative hydatid serology, cyst size …