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For: Moirand R, Jouanolle AM, Brissot P, Le Gall JY, David V, Deugnier Y. Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives. Gastroenterology. 1999;116:372-377. [PMID: 9922318 DOI: 10.1016/s0016-5085(99)70134-4] [Cited by in Crossref: 91] [Cited by in F6Publishing: 11] [Article Influence: 4.1] [Reference Citation Analysis]
Number Citing Articles
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2 Milet J, Dehais V, Bourgain C, Jouanolle AM, Mosser A, Perrin M, Morcet J, Brissot P, David V, Deugnier Y, Mosser J. Common variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetrance. Am J Hum Genet 2007;81:799-807. [PMID: 17847004 DOI: 10.1086/520001] [Cited by in Crossref: 95] [Cited by in F6Publishing: 81] [Article Influence: 6.8] [Reference Citation Analysis]
3 Bozkaya H, Bektas M, Metin O, Erkan O, Ibrahimoglu D, Dalva K, Akbiyik F, Gurel S, Bozdayi AM, Akay C, Yurdaydin C, Aslan O, Uzunalimoglu O. Screening for hemochromatosis in Turkey. Dig Dis Sci 2004;49:444-9. [PMID: 15139495 DOI: 10.1023/b:ddas.0000020500.26184.ce] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
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6 Egger NG, Goeger DE, Payne DA, Miskovsky EP, Weinman SA, Anderson KE. Porphyria cutanea tarda: multiplicity of risk factors including HFE mutations, hepatitis C, and inherited uroporphyrinogen decarboxylase deficiency. Dig Dis Sci. 2002;47:419-426. [PMID: 11855561 DOI: 10.1023/a:1013746828074] [Cited by in Crossref: 60] [Cited by in F6Publishing: 13] [Article Influence: 3.2] [Reference Citation Analysis]
7 Porto G, Brissot P, Swinkels DW, Zoller H, Kamarainen O, Patton S, Alonso I, Morris M, Keeney S. EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). Eur J Hum Genet 2016;24:479-95. [PMID: 26153218 DOI: 10.1038/ejhg.2015.128] [Cited by in Crossref: 41] [Cited by in F6Publishing: 23] [Article Influence: 6.8] [Reference Citation Analysis]
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9 Vassiliadis T, Garipidou V, Perifanis V, Tziomalos K, Giouleme O, Patsiaoura K, Avramidis M, Nikolaidis N, Vakalopoulou S, Tsitouridis I, Antoniadis A, Semertzidis P, Kioumi A, Premetis E, Eugenidis N. A case of successful management with splenectomy of intractable ascites due to congenital dyserythropoietic anemia type II-induced cirrhosis. World J Gastroenterol 2006;12:818-21. [PMID: 16521204 DOI: 10.3748/wjg.v12.i5.818] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
10 Adams PC. Population screening for haemochromatosis. Gut 2000;46:301-3. [PMID: 10673284 DOI: 10.1136/gut.46.3.301] [Cited by in Crossref: 34] [Cited by in F6Publishing: 32] [Article Influence: 1.6] [Reference Citation Analysis]
11 Yönal O, Hatirnaz O, Akyüz F, Ozbek U, Demir K, Kaymakoglu S, Okten A, Mungan Z. HFE gene mutation, chronic liver disease, and iron overload In Turkey. Dig Dis Sci 2007;52:3298-302. [PMID: 17410459 DOI: 10.1007/s10620-006-9683-2] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]