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Results: 1 to 20 of 101

Similar articles for PubMed (Select 23651750)

1.

[Juvenile haemochromatosis caused by a homozygous Gly320Val mutation in the haemojuvelin gene].

Berg LB, Milman NT, Friis-Hansen L, Jensen PD, Fründ T.

Ugeskr Laeger. 2013 Apr 15;175(16):1113-4. Danish.

PMID:
23651750
2.

[Genetic iron overloads and hepatic insulin-resistance iron overload syndrome: an update].

Ruivard M.

Rev Med Interne. 2009 Jan;30(1):35-42. doi: 10.1016/j.revmed.2008.05.004. Epub 2008 Jun 26. Review. French.

PMID:
18584923
3.

Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.

Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.

Blood Cells Mol Dis. 2011 Apr 15;46(4):302-7. doi: 10.1016/j.bcmd.2011.02.008.

PMID:
21411349
4.

[Diagnosis and treatment of primary hemochromatosis].

Swinkels DW, Marx JJ.

Ned Tijdschr Geneeskd. 1999 Jul 3;143(27):1404-8. Review. Dutch.

PMID:
10422553
5.

A juvenile hemochromatosis patient homozygous for a novel deletion of cDNA nucleotide 81 of hemojuvelin.

Lee P, Promrat K, Mallette C, Flynn M, Beutler E.

Acta Haematol. 2006;115(1-2):123-7.

PMID:
16424663
6.

Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.

Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.

Eur J Immunogenet. 2000 Jun;27(3):129-34.

PMID:
10940080
7.

[Diagnosis of 5 patients with possible primary hemochromatosis].

Jacobs EM, de Vries RA, Elving LD, Stalenhoef AF, Swinkels DW.

Ned Tijdschr Geneeskd. 2003 Apr 5;147(14):666-70. Dutch.

PMID:
12712652
8.

Diagnosis and management of genetic haemochromatosis.

Dooley JS.

Best Pract Res Clin Haematol. 2002 Jun;15(2):277-93. Review.

PMID:
12401308
9.

Hereditary haemochromatosis: detection and management.

Vautier G, Murray M, Olynyk JK.

Med J Aust. 2001 Oct 15;175(8):418-21. Review.

PMID:
11700835
10.

[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. doi: 10.4045/tidsskr.08.0084. Review. Norwegian.

11.

Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.

Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.

Isr Med Assoc J. 2004 Jan;6(1):30-3.

12.

Homozygous G320V mutation in the HJV gene causing juvenile hereditary haemochromatosis type A. A case report.

Militaru MS, Popp RA, Trifa AP.

J Gastrointestin Liver Dis. 2010 Jun;19(2):191-3.

13.

[Primary hemochromatosis in asymptomatic young patients].

Muñoz Sánchez MM, Núñez Martínez O, Torres Orgaz A, del Castillo Rueda A, de Portugal Alvarez J.

An Med Interna. 2000 Jan;17(1):9-12. Spanish.

PMID:
10730398
14.

Clinical expression of haemochromatosis in Irish C282Y homozygotes identified through family screening.

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

Eur J Gastroenterol Hepatol. 2004 Sep;16(9):859-63.

PMID:
15316409
15.

[Hereditary hemochromatosis].

Niederau C.

Med Klin (Munich). 2009 Dec 15;104(12):931-46. doi: 10.1007/s00063-009-1192-6. Review. German.

PMID:
20039160
16.

Hemochromatosis and iron-overload screening in a racially diverse population.

Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P; Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.

N Engl J Med. 2005 Apr 28;352(17):1769-78.

17.

Clinical expression of C282Y homozygous HFE haemochromatosis at 14 years of age.

Rossi E, Wallace DF, Subramaniam VN, St Pierre TG, Mews C, Jeffrey GP.

Ann Clin Biochem. 2006 May;43(Pt 3):233-6.

PMID:
16704763
18.

[Hereditary hemochromatosis: molecular diagnosis and effect of treatment].

Szczeklik W, Dropiński J, Dziedzina S, Szułdrzyński K, Biesiada G, Mach T, Sanak M.

Pol Arch Med Wewn. 2004 May;111(5):593-6. Polish.

PMID:
15508811
20.

[Long-term survival of 2 cases of hemochromatosis respectively homozygous for His63Asp and Cys282Tyr mutations].

Samii K, Darbellay R, Trachsel H, Beris P.

Schweiz Med Wochenschr. 1997 Nov 8;127(45):1867-70. French.

PMID:
9446207
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