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Items: 1 to 20 of 87

1.

Diagnosis and treatment difficulties in 18-year-old male patient with hereditary hemochromatosis, chronic hepatitis B, Gilbert syndrome and ulcerative colitis.

Sikorska K, Liberek A, Romanowski T, Szlagatys-Sidorkiewicz A, Landowski P, Bielawski KP.

Acta Biochim Pol. 2011;58(2):251-4. Epub 2011 Jun 2.

2.

Diagnosis and treatment of a 16-year-old Chinese patient with concurrent hereditary hemochromatosis and Gilbert's syndrome.

Wang X, Liu Y, Chang Y, Liu H, Wang P.

Eur J Med Res. 2014 Sep 28;19:51. doi: 10.1186/s40001-014-0051-y.

3.

Hemochromatosis mutations in Iranians with hepatitis B virus infection.

Sendi H, Ghaziani T, Zali MR, Adibi P, Agah M, Jazayeri M, Shahraz S, Magnius L, Bonkovsky HL.

Clin Infect Dis. 2005 Feb 1;40(3):e19-21. Epub 2004 Dec 29.

PMID:
15668853
4.
5.

[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
6.

TATA-Box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with clinical diagnosis of Gilbert Syndrome.

Costa E, Vieira E, Santos-Silva E, Barbot J, dos Santos R.

Haematologica. 2002 Apr;87(4):ELT21. No abstract available.

PMID:
11940506
7.

[Diagnostic difficulties of the HFE hemochromatosis gene (delay, excess, absence): the patient perspective].

Fajardy I, Michel H.

Ann Biol Clin (Paris). 2012 Jul-Aug;70(4):492-5. French. No abstract available.

8.

When and how should we screen for hereditary hemochromatosis?

Chalès G, Guggenbuhl P.

Joint Bone Spine. 2003 Aug;70(4):263-70. Review.

PMID:
12951308
10.

Concomitant presentation of collagenous sprue and HFE hemochromatosis.

Parisian KR, Plesec TP, Fairbanks KD, Tavill AS, Shen B.

J Crohns Colitis. 2011 Aug;5(4):369-72. doi: 10.1016/j.crohns.2011.03.009. Epub 2011 Apr 29.

PMID:
21683310
11.

Case report of HFE gene testing for the diagnosis of hereditary hemochromatosis.

Pan HY, Wang LJ.

J Dig Dis. 2011 Oct;12(5):409-11. doi: 10.1111/j.1751-2980.2011.00515.x. No abstract available.

PMID:
21955435
12.

Coexistence of HFE and rare UGT1A1 genes mutations in patients with iron overload related liver injury.

Sikorska K, Romanowski T, Stalke P, Jaskiewicz K, Bielawski KP.

Adv Med Sci. 2010;55(1):108-10. doi: 10.2478/v10039-010-0003-x.

PMID:
20371435
13.

Incorrect diagnosis of hereditary hemochromatosis.

Mirochnik O, Halim-Kertanegara N, Hertzberg M, McDonald D, Liddle C.

Am J Hematol. 2000 Feb;63(2):104-5. No abstract available.

PMID:
10629581
14.

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

Valenti L, Maggioni P, Piperno A, Rametta R, Pelucchi S, Mariani R, Dongiovanni P, Fracanzani AL, Fargion S.

World J Gastroenterol. 2012 Jun 14;18(22):2813-20. doi: 10.3748/wjg.v18.i22.2813.

15.

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.

16.

Hemochromatosis gene modifies course of hepatitis C viral infection.

Pietrangelo A.

Gastroenterology. 2003 May;124(5):1509-23. Review. No abstract available.

PMID:
12730889
17.

Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome.

Trioche P, Chalas J, Francoual J, Capel L, Lindenbaum A, Odièvre M, Labrune P.

Arch Dis Child. 1999 Oct;81(4):301-3.

18.

[Detection of HFE polymorphism in German patients with hereditary hemochromatosis].

Mensing HJ.

Dtsch Med Wochenschr. 2000 Nov 3;125(44):1346-7. German. No abstract available.

PMID:
11109420
19.

[Genetic screening of hereditary hemochromatosis in Spain. Current situation].

Altés A.

Med Clin (Barc). 2005 Jul 2;125(5):184-6. Spanish. No abstract available.

PMID:
16153360

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