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Items: 18

1.

Should we use proton pump inhibitors as an add-on treatment in hereditary hemochromatosis?

Kani HT, Gündüz F.

Turk J Gastroenterol. 2018 Mar;29(2):254-255. doi: 10.5152/tjg.2018.17713. No abstract available.

PMID:
29749343
2.

Haemochromatosis: Pathophysiology and the red blood cell1.

Richardson KJ, McNamee AP, Simmonds MJ.

Clin Hemorheol Microcirc. 2018;69(1-2):295-304. doi: 10.3233/CH-189128.

PMID:
29660923
3.

Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.

Olsson KS, Wålinder O, Jansson U, Wilbe M, Bondeson ML, Stattin EL, Raha-Chowdhury R, Williams R.

Hereditas. 2017 Dec 19;154:16. doi: 10.1186/s41065-017-0052-2. eCollection 2017.

4.

Comment on: Hereditary haemochromatosis arthropathy and Doppler ultrasound findings of synovitis: reply.

Oke AR, Wong E, Young-Min S.

Rheumatology (Oxford). 2018 Apr 1;57(4):766-767. doi: 10.1093/rheumatology/kex437. No abstract available.

PMID:
29228396
5.

Comment on: Hereditary hemochromatosis arthropathy and Doppler ultrasound findings of synovitis.

Parperis K.

Rheumatology (Oxford). 2018 Apr 1;57(4):765-766. doi: 10.1093/rheumatology/kex436. No abstract available.

PMID:
29228359
6.

Genetic hemochromatosis: Pathophysiology, diagnostic and therapeutic management.

Brissot P, Cavey T, Ropert M, Guggenbuhl P, Loréal O.

Presse Med. 2017 Dec;46(12 Pt 2):e288-e295. doi: 10.1016/j.lpm.2017.05.037. Epub 2017 Nov 20. Review.

PMID:
29158016
7.

Characterization of three novel pathogenic SLC40A1 mutations and genotype/phenotype correlations in 7 Italian families with type 4 hereditary hemochromatosis.

Majore S, Bonaccorsi di Patti MC, Valiante M, Polticelli F, Cortese A, Di Bartolomeo S, De Bernardo C, De Muro M, Faienza F, Radio FC, Grammatico P, Musci G.

Biochim Biophys Acta. 2018 Feb;1864(2):464-470. doi: 10.1016/j.bbadis.2017.11.006. Epub 2017 Nov 14.

PMID:
29154924
8.

The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis.

Kawabata H.

Int J Hematol. 2018 Jan;107(1):31-43. doi: 10.1007/s12185-017-2365-3. Epub 2017 Nov 13. Review.

PMID:
29134618
9.

Ethnic and genetic factors of iron status in women of reproductive age.

Gordeuk VR, Brannon PM.

Am J Clin Nutr. 2017 Dec;106(Suppl 6):1594S-1599S. doi: 10.3945/ajcn.117.155853. Epub 2017 Oct 25.

PMID:
29070555
10.

Ultrasound verified inflammation and structural damage in patients with hereditary haemochromatosis-related arthropathy.

Dejaco C, Stadlmayr A, Duftner C, Trimmel V, Husic R, Krones E, Zandieh S, Husar-Memmer E, Zollner G, Hermann J, Gretler J, Lackner A, Ficjan A, Datz C, Axman R, Zwerina J.

Arthritis Res Ther. 2017 Oct 24;19(1):243. doi: 10.1186/s13075-017-1448-0.

11.

From the bottom of the heart: Measuring liver iron concentration on cardiac MRI.

Tan S, Peng Q, Liszewski MC, Taragin BH.

Clin Imaging. 2018 Jan - Feb;47:124-129. doi: 10.1016/j.clinimag.2017.09.008. Epub 2017 Sep 13.

PMID:
28946103
12.

Duodenal cytochrome b (Cybrd1) ferric reductase functional studies in cells.

Schlottmann F, Vera-Aviles M, Latunde-Dada GO.

Metallomics. 2017 Oct 18;9(10):1389-1393. doi: 10.1039/c7mt00254h.

PMID:
28937159
13.
14.

Clinical and Laboratory Associations with Persistent Hyperferritinemia in 373 Black Hemochromatosis and Iron Overload Screening Study Participants.

Barton JC, Barton JC, Adams PC.

Ann Hepatol. 2017 Sep-Oct;16(5):802-811. doi: 10.5604/01.3001.0010.2815.

15.

Impaired Transmigration of Myeloid-Derived Suppressor Cells across Human Sinusoidal Endothelium Is Associated with Decreased Expression of CD13.

Resheq YJ, Menzner AK, Bosch J, Tickle J, Li KK, Wilhelm A, Hepburn E, Murihead G, Ward ST, Curbishley SM, Zimmermann HW, Bruns T, Gilbert DF, Tripal P, Mackensen A, Adams DH, Weston CJ.

J Immunol. 2017 Sep 1;199(5):1672-1681. doi: 10.4049/jimmunol.1600466. Epub 2017 Jul 24.

PMID:
28739875
16.

HFE gene polymorphism defined by sequence-based typing of the Brazilian population and a standardized nomenclature for HFE allele sequences.

Campos WN, Massaro JD, Martinelli ALC, Halliwell JA, Marsh SGE, Mendes-Junior CT, Donadi EA.

HLA. 2017 Oct;90(4):238-242. doi: 10.1111/tan.13097. Epub 2017 Aug 4.

PMID:
28727322
17.

Hemochromatosis, iron-loading anemia, and SMAD.

Gordeuk VR.

Blood. 2017 Jul 6;130(1):6-7. doi: 10.1182/blood-2017-05-782656. No abstract available.

PMID:
28684448
18.

Heart and heart-liver transplantation in patients with hemochromatosis.

Robinson MR, Al-Kindi SG, Oliveira GH.

Int J Cardiol. 2017 Oct 1;244:226-228. doi: 10.1016/j.ijcard.2017.06.075. Epub 2017 Jun 21.

PMID:
28655414

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