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Similar articles for PubMed (Select 15842597)

1.

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. Review.

PMID:
15842597
2.

[Non-HFE-related hereditary iron overload].

Aguilar-Martinez P.

Presse Med. 2007 Sep;36(9 Pt 2):1279-91. Epub 2007 May 30. Review. French.

PMID:
17540536
3.

[Hyperferritinemia-cataract syndrome associated to the HFE gene mutation. Two new Spanish families and a new mutation (A37T: "Zaragoza")].

García Erce JA, Cortés T, Cremonesi L, Cazzola M, Pérez-Lungmus G, Giralt M.

Med Clin (Barc). 2006 Jun 10;127(2):55-8. Spanish.

PMID:
16900584
5.

Global sequencing approach for characterizing the molecular background of hereditary iron disorders.

Cunat S, Giansily-Blaizot M, Bismuth M, Blanc F, Dereure O, Larrey D, Quellec AL, Pouderoux P, Rose C, Raingeard I, Renard E, Schved JF, Aguilar-Martinez P; CHU Montpellier AOI 2004 Working Group.

Clin Chem. 2007 Dec;53(12):2060-9. Epub 2007 Oct 19.

6.

[Genetics of hereditary iron overload].

Le Gall JY, Jouanolle AM, Fergelot P, Mosser J, David V.

Bull Acad Natl Med. 2004;188(2):247-62; discussion 262-3. Review. French.

PMID:
15506716
7.

Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes.

Mendes AI, Ferro A, Martins R, Picanço I, Gomes S, Cerqueira R, Correia M, Nunes AR, Esteves J, Fleming R, Faustino P.

Ann Hematol. 2009 Mar;88(3):229-34. doi: 10.1007/s00277-008-0572-y. Epub 2008 Sep 2.

PMID:
18762941
8.

Rare causes of hereditary iron overload.

Ponka P.

Semin Hematol. 2002 Oct;39(4):249-62. Review.

PMID:
12382200
9.

[Hereditary and acquired iron overload].

de Korwin JD.

Nephrol Ther. 2006 Nov;2 Suppl 5:S304-12. French.

PMID:
17373275
10.

Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA.

Cazzola M, Bergamaschi G, Tonon L, Arbustini E, Grasso M, Vercesi E, Barosi G, Bianchi PE, Cairo G, Arosio P.

Blood. 1997 Jul 15;90(2):814-21.

11.

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;78(1):66-71. Epub 2006 Oct 17.

PMID:
17042772
12.

Dual diagnoses of hereditary hyperferritinaemia-cataract syndrome and hereditary haemochromatosis.

Hughes M, Vosylius P.

Clin Lab Haematol. 2006 Oct;28(5):357-9.

PMID:
16999731
13.
14.

Hepatic iron metabolism gene expression profiles in HFE associated hereditary hemochromatosis.

Gleeson F, Ryan E, Barrett S, Russell J, Crowe J.

Blood Cells Mol Dis. 2007 Jan-Feb;38(1):37-44. Epub 2006 Nov 13.

PMID:
17098454
15.

Hyperferritinemia, iron overload, and multiple metabolic alterations identify patients at risk for nonalcoholic steatohepatitis.

Fargion S, Mattioli M, Fracanzani AL, Sampietro M, Tavazzi D, Fociani P, Taioli E, Valenti L, Fiorelli G.

Am J Gastroenterol. 2001 Aug;96(8):2448-55.

PMID:
11513189
16.

Non-HFE haemochromatosis.

Wallace DF, Subramaniam VN.

World J Gastroenterol. 2007 Sep 21;13(35):4690-8. Review.

17.

HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.

Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.

Genet Test. 2007 Fall;11(3):269-75.

PMID:
17949288
18.

Inherited iron loading: genetic testing in diagnosis and management.

Worwood M.

Blood Rev. 2005 Mar;19(2):69-88. Review.

PMID:
15603911
19.

Rare types of genetic hemochromatosis.

Camaschella C, Poggiali E.

Acta Haematol. 2009;122(2-3):140-5. doi: 10.1159/000243798. Epub 2009 Nov 10.

PMID:
19907151
20.

Genetic background of primary iron overload syndromes in Japan.

Hayashi H, Wakusawa S, Motonishi S, Miyamoto K, Okada H, Inagaki Y, Ikeda T.

Intern Med. 2006;45(20):1107-11. Epub 2006 Nov 15. Review.

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