These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
109 related articles for article (PubMed ID: 12467562)
1. [Congenital hyperferritinemia and cataract syndrome]. García-Erce JA An Esp Pediatr; 2002 Nov; 57(5):497-8; author reply 498-500. PubMed ID: 12467562 [No Abstract] [Full Text] [Related]
2. [Isolated hyperferritinemia in a healthy male infant: hereditary hyperferritinemia-cataract syndrome]. Cervera Bravo A; Sebastían Planas M; Alarabe Alarabe A; Díez Sáenz A; Avilés Egea MJ; Balas Pérez A An Esp Pediatr; 2000 Mar; 52(3):267-70. PubMed ID: 11003906 [TBL] [Abstract][Full Text] [Related]
3. A new family with hereditary hyperferritinemia cataract syndrome. Tuysuz G; Ozdemir N; Sonmez E; Kannengiesser C; Celkan T Genet Couns; 2013; 24(4):393-7. PubMed ID: 24551982 [TBL] [Abstract][Full Text] [Related]
4. Hereditary hyperferritinemia cataract syndrome as a cause of childhood hyperferritinemia. Tsantoula F; Kioumi A; Germenis AE; Speletas M J Pediatr Hematol Oncol; 2014 Jul; 36(5):e304-6. PubMed ID: 24983587 [TBL] [Abstract][Full Text] [Related]
5. Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene. Arosio C; Fossati L; Viganò M; Trombini P; Cazzaniga G; Piperno A Haematologica; 1999 Jun; 84(6):560-1. PubMed ID: 10366804 [No Abstract] [Full Text] [Related]
6. [New mutation in a Spanish family with hereditary hyperferritinemia-cataract syndrome]. Santotoribio JD; García de la Torre Á; Cañavate Solano C; Toral Peña A Med Clin (Barc); 2014 Jan; 142(2):93. PubMed ID: 24022025 [No Abstract] [Full Text] [Related]
10. Prevalence of hereditary hyperferritinemia-cataract syndrome in blood donors and patients with cataract. Bozzini C; Galbiati S; Tinazzi E; Aldigeri R; De Matteis G; Girelli D Haematologica; 2003 Feb; 88(2):219-20. PubMed ID: 12604412 [No Abstract] [Full Text] [Related]
11. [Hyperferritinemia, ferropenia and metabolic syndrome in a patient with a new mutation of gene TFR2 and another in gene FTL. A family study]. Del Castillo-Rueda A; Moreno-Carralero MI; Cuadrado-Grande N; Méndez M; Morán-Jiménez MJ Med Clin (Barc); 2011 Jun; 137(2):68-72. PubMed ID: 21524769 [TBL] [Abstract][Full Text] [Related]
12. Hereditary hyperferritinemia cataract syndrome in four patients with mutations in the IRE of the FTL gene. Muñoz-Muñoz J; Cuadrado-Grande N; Moreno-Carralero MI; Hoyos-Sanabria B; Manubes-Guarch A; González AF; Tejada-Palacios P; Del-Castillo-Rueda A; Morán-Jiménez MJ Clin Genet; 2013 May; 83(5):491-3. PubMed ID: 22881709 [No Abstract] [Full Text] [Related]
13. Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome. Aslan D; Akata RF; Atalay HT; Üçgül AY Pediatr Hematol Oncol; 2019 Sep; 36(6):390-393. PubMed ID: 31522592 [TBL] [Abstract][Full Text] [Related]
14. A novel deletion in the iron-response element of the L-ferritin gene, causing hyperferritinaemia cataract syndrome. Garber I; Pudek M Ann Clin Biochem; 2014 Nov; 51(Pt 6):710-3. PubMed ID: 24936091 [TBL] [Abstract][Full Text] [Related]
15. Hyperferritinemia-cataract syndrome: Long-term ophthalmic observations in an Italian family. Cosentino I; Zeri F; Swann PG; Majore S; Radio FC; Palumbo P; Grammatico P; Petitti V Ophthalmic Genet; 2016 Sep; 37(3):318-22. PubMed ID: 26849797 [TBL] [Abstract][Full Text] [Related]
16. [Hereditary hyperferritinemia cataract syndrome]. Holzgreve H Dtsch Med Wochenschr; 2011 Sep; 136(38):1895-8. PubMed ID: 21915803 [TBL] [Abstract][Full Text] [Related]
17. [Hereditary hyperferritinemia-cataract syndrome. Unusual differential diagnosis of unexplainable high levels of ferritin]. Vaktnäs J; Olsson M Lakartidningen; 2013 Dec 13-2014 Jan 7; 110(51-52):2302-3. PubMed ID: 24501909 [No Abstract] [Full Text] [Related]
18. [Congenital cataract syndrome and hyperferritinemia]. García-Erce JA; Salvador-Osuna C; Cortés T; Pérez-Lungmus G Med Clin (Barc); 1999 Mar; 112(10):398. PubMed ID: 10227023 [No Abstract] [Full Text] [Related]