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Results: 1 to 20 of 122

1.

Highly sensitivity adhesion molecules detection in hereditary haemochromatosis patients reveals altered expression.

Norris S, White M, Mankan AK, Lawless MW.

Int J Immunogenet. 2010 Apr;37(2):125-33. doi: 10.1111/j.1744-313X.2010.00904.x. Epub 2010 Feb 19.

PMID:
20193033
[PubMed - indexed for MEDLINE]
2.

Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.

Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.

Tissue Antigens. 2007 Oct;70(4):294-300.

PMID:
17767550
[PubMed - indexed for MEDLINE]
3.

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
[PubMed - indexed for MEDLINE]
4.

Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.

Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.

BMC Med Genet. 2007 Nov 23;8:69.

PMID:
18036208
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.

Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.

Eur J Haematol. 2001 Aug;67(2):110-8.

PMID:
11722599
[PubMed - indexed for MEDLINE]
6.

Plasma soluble adhesion molecules; intercellular adhesion molecule-1, vascular cell adhesion molecule-1 and E-selectin levels in patients with isolated coronary artery ectasia.

Turhan H, Erbay AR, Yasar AS, Aksoy Y, Bicer A, Yetkin G, Yetkin E.

Coron Artery Dis. 2005 Feb;16(1):45-50.

PMID:
15654200
[PubMed - indexed for MEDLINE]
7.

Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.

Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.

Immunogenetics. 1998 Apr;47(5):404-10.

PMID:
9510559
[PubMed - indexed for MEDLINE]
8.

[Molecular genetic diagnostics and screening of hereditary hemochromatosis].

Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.

Vnitr Lek. 2006 Jun;52(6):602-8. Slovak.

PMID:
16871764
[PubMed - indexed for MEDLINE]
9.

A distinct profile of six soluble adhesion molecules (ICAM-1, ICAM-3, VCAM-1, E-selectin, L-selectin and P-selectin) in rheumatoid arthritis.

Littler AJ, Buckley CD, Wordsworth P, Collins I, Martinson J, Simmons DL.

Br J Rheumatol. 1997 Feb;36(2):164-9.

PMID:
9133922
[PubMed - indexed for MEDLINE]
Free Article
10.

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.

Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.

Scand J Clin Lab Invest. 2002;62(7):527-35.

PMID:
12512743
[PubMed - indexed for MEDLINE]
11.
12.

HFE mutations, iron deficiency and overload in 10,500 blood donors.

Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.

Br J Haematol. 2001 Aug;114(2):474-84.

PMID:
11529872
[PubMed - indexed for MEDLINE]
13.

[Serum soluble adhesion molecules in patients with sarcoidosis].

Mukae H, Ashitani J, Ihiboshi H, Taniguchi H, Matsukura S, Iida K, Kadota J, Kohno S.

Nihon Kyobu Shikkan Gakkai Zasshi. 1997 Nov;35(11):1186-90. Japanese.

PMID:
9493444
[PubMed - indexed for MEDLINE]
14.

Increased DMT1 but not IREG1 or HFE mRNA following iron depletion therapy in hereditary haemochromatosis.

Kelleher T, Ryan E, Barrett S, Sweeney M, Byrnes V, O'Keane C, Crowe J.

Gut. 2004 Aug;53(8):1174-9.

PMID:
15247188
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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
[PubMed - indexed for MEDLINE]
16.

Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).

Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.

Genet Mol Res. 2005 Mar 31;4(1):31-8.

PMID:
15841433
[PubMed - indexed for MEDLINE]
Free Article
17.

Differential patterns of circulating adhesion molecules in children with bronchial asthma and acute bronchiolitis.

Oymar K, Bjerknes R.

Pediatr Allergy Immunol. 1998 May;9(2):73-9.

PMID:
9677602
[PubMed - indexed for MEDLINE]
18.

Increased plasma soluble adhesion molecules; ICAM-1, VCAM-1, and E-selectin levels in patients with slow coronary flow.

Turhan H, Saydam GS, Erbay AR, Ayaz S, Yasar AS, Aksoy Y, Basar N, Yetkin E.

Int J Cardiol. 2006 Apr 4;108(2):224-30. Epub 2005 Jul 5.

PMID:
16002164
[PubMed - indexed for MEDLINE]
19.

HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls.

de Juan D, Reta A, Castiella A, Pozueta J, Prada A, Cuadrado E.

Eur J Hum Genet. 2001 Dec;9(12):961-4.

PMID:
11840200
[PubMed - indexed for MEDLINE]
Free Article
20.

Adhesion molecules in patients with coronary artery disease and moderate-to-severe obstructive sleep apnea.

El-Solh AA, Mador MJ, Sikka P, Dhillon RS, Amsterdam D, Grant BJ.

Chest. 2002 May;121(5):1541-7.

PMID:
12006441
[PubMed - indexed for MEDLINE]

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