This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Email citation

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Case Reports

. 2000 Apr;109(1):252-3.

doi: 10.1046/j.1365-2141.2000.01987.x.

A case of non-HFE juvenile haemochromatosis presenting with adrenocortical insufficiency

J Varkonyi, J P Kaltwasser, C Seidl, G Kollai, H Andrikovics, A Tordai

PMID: 10896410
DOI: 10.1046/j.1365-2141.2000.01987.x

Free article

Case Reports

A case of non-HFE juvenile haemochromatosis presenting with adrenocortical insufficiency

J Varkonyi et al. Br J Haematol. 2000 Apr.

Free article

. 2000 Apr;109(1):252-3.

doi: 10.1046/j.1365-2141.2000.01987.x.

Authors

J Varkonyi, J P Kaltwasser, C Seidl, G Kollai, H Andrikovics, A Tordai

PMID: 10896410
DOI: 10.1046/j.1365-2141.2000.01987.x

No abstract available

PubMed Disclaimer

Similar articles

Haemochromatosis, HFE and genetic complexity.
Risch N. Risch N. Nat Genet. 1997 Dec;17(4):375-6. doi: 10.1038/ng1297-375. Nat Genet. 1997. PMID: 9398831 Review. No abstract available.
HFE genotype in patients with hemochromatosis and other liver diseases.
McLaren GD. McLaren GD. Ann Intern Med. 2000 Feb 1;132(3):245; author reply 246. doi: 10.7326/0003-4819-132-3-200002010-00017. Ann Intern Med. 2000. PMID: 10651611 No abstract available.
HFE genotype in patients with hemochromatosis and other liver diseases.
Powell LW. Powell LW. Ann Intern Med. 2000 Feb 1;132(3):245-6. doi: 10.7326/0003-4819-132-3-200002010-00018. Ann Intern Med. 2000. PMID: 10651612 No abstract available.
Clinical haemochromatosis in HFE mutation carriers.
Poullis A, Moodie SJ, Maxwell JD. Poullis A, et al. Lancet. 2002 Aug 3;360(9330):411-2; author reply 413-4. doi: 10.1016/s0140-6736(02)09581-8. Lancet. 2002. PMID: 12241803 No abstract available.
Diagnosis and management of haemochromatosis since the discovery of the HFE gene: a European experience.
[No authors listed] [No authors listed] Br J Haematol. 2000 Jan;108(1):31-9. doi: 10.1046/j.1365-2141.2000.01687.x. Br J Haematol. 2000. PMID: 10651721 Review. No abstract available.

See all similar articles

Cited by

Epidemiology, pathogenesis, and diagnosis of Addison's disease in adults.
Betterle C, Presotto F, Furmaniak J. Betterle C, et al. J Endocrinol Invest. 2019 Dec;42(12):1407-1433. doi: 10.1007/s40618-019-01079-6. Epub 2019 Jul 18. J Endocrinol Invest. 2019. PMID: 31321757 Review.
Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population.
Barton JC, Rivers CA, Niyongere S, Bohannon SB, Acton RT. Barton JC, et al. BMC Med Genet. 2004 Dec 20;5:29. doi: 10.1186/1471-2350-5-29. BMC Med Genet. 2004. PMID: 15610558 Free PMC article.
Endocrine dysfunction in hereditary hemochromatosis.
Pelusi C, Gasparini DI, Bianchi N, Pasquali R. Pelusi C, et al. J Endocrinol Invest. 2016 Aug;39(8):837-47. doi: 10.1007/s40618-016-0451-7. Epub 2016 Mar 7. J Endocrinol Invest. 2016. PMID: 26951056 Review.

Publication types

Actions
Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions
Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Ovid Technologies, Inc.
- Wiley
Medical
- MedlinePlus Health Information