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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
137 related items for PubMed ID: 16910257
1. [Management of hyperferritinemia]. Delwaide J, Giet D, Lamproye A, Belaïche J. Rev Med Liege; 2006; 61(5-6):329-33. PubMed ID: 16910257 [Abstract] [Full Text] [Related]
6. [Diagnosis of an increased serum level of ferritin]. Lorcerie B, Audia S, Samson M, Millière A, Falvo N, Leguy-Seguin V, Berthier S, Bonnotte B. Rev Med Interne; 2015 Aug; 36(8):522-9. PubMed ID: 25640247 [Abstract] [Full Text] [Related]
7. The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities. Aguilar-Martinez P, Schved JF, Brissot P. Am J Gastroenterol; 2005 May; 100(5):1185-94. PubMed ID: 15842597 [Abstract] [Full Text] [Related]
8. Diagnosis of hyperferritinemia in routine clinical practice. Lorcerie B, Audia S, Samson M, Millière A, Falvo N, Leguy-Seguin V, Berthier S, Bonnotte B. Presse Med; 2017 Dec; 46(12 Pt 2):e329-e338. PubMed ID: 29150231 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
11. [Biology and genetics of iron metabolism abnormalities. 7th Joint Meeting Inserm-SFBC. Paris, 27 November 1997]. Brissot P. Ann Biol Clin (Paris); 1998 Jul; 56 Spec No():4. PubMed ID: 9867723 [No Abstract] [Full Text] [Related]
12. Hyperferritinemia increases the risk of hyperuricemia in HFE-hereditary hemochromatosis. Flais J, Bardou-Jacquet E, Deugnier Y, Coiffier G, Perdriger A, Chalès G, Ropert M, Loréal O, Guggenbuhl P. Joint Bone Spine; 2017 May; 84(3):293-297. PubMed ID: 27659401 [Abstract] [Full Text] [Related]
16. [Hemochromatosis--from an underdiagnosed curiosity to a common disease]. Hagve TA, Asberg A, Ulvik R, Borch-Iohnsen B, Thorstensen K. Tidsskr Nor Laegeforen; 2009 Apr 30; 129(9):863-6. PubMed ID: 19415085 [Abstract] [Full Text] [Related]
20. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload? de Diego C, Opazo S, Murga MJ, Martínez-Castro P. Eur J Haematol; 2007 Jan 23; 78(1):66-71. PubMed ID: 17042772 [Abstract] [Full Text] [Related] Page: [Next] [New Search]