메뉴 건너뛰기




Volumn 49, Issue 3, 2012, Pages 211-213

Hyperferritinaemia; laboratory implications

Author keywords

[No Author keywords available]

Indexed keywords

APOFERRITIN; C PEPTIDE; CERULOPLASMIN; FERRITIN; FERROPORTIN; HEPCIDIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; INTERLEUKIN 1ALPHA; IRON; PROTON COUPLED FOLATE TRANSPORTER; TRANSFERRIN; TRANSFERRIN RECEPTOR; TUMOR NECROSIS FACTOR ALPHA;

EID: 84861496737     PISSN: 00045632     EISSN: 17581001     Source Type: Journal    
DOI: 10.1258/acb.2012.012059     Document Type: Editorial
Times cited : (9)

References (28)
  • 1
    • 84861508736 scopus 로고    scopus 로고
    • Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assay
    • Thurlow V, Vadher B, Bomford A, et al. Two novel mutations in the L ferritin coding sequence associated with benign hyperferritinaemia unmasked by glycosylated ferritin assay. Ann Clin Biochem 2012;49: 302-5
    • (2012) Ann Clin Biochem , vol.49 , pp. 302-305
    • Thurlow, V.1    Vadher, B.2    Bomford, A.3
  • 4
    • 19144362107 scopus 로고    scopus 로고
    • The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities
    • Aguilar-Martinez P, Schved JF, Brissot P. The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities. Am J Gastroenterol 2005;100:1185-94
    • (2005) Am J Gastroenterol , vol.100 , pp. 1185-1194
    • Aguilar-Martinez, P.1    Schved, J.F.2    Brissot, P.3
  • 6
    • 62949152341 scopus 로고    scopus 로고
    • Towards explaining 'unexplained hyperferritinemia'
    • Camaschella C, Poggiali E. Towards explaining 'unexplained hyperferritinemia'. Haematologica 2009;94:307-9
    • (2009) Haematologica , vol.94 , pp. 307-309
    • Camaschella, C.1    Poggiali, E.2
  • 7
    • 0022974645 scopus 로고
    • Plasma ferritin determination as a diagnostic tool
    • Finch CA, Bellotti V, Stray S, et al. Plasma ferritin determination as a diagnostic tool. West J Med 1986;145:657-63
    • (1986) West J Med , vol.145 , pp. 657-663
    • Finch, C.A.1    Bellotti, V.2    Stray, S.3
  • 8
    • 74049103621 scopus 로고    scopus 로고
    • Plasma ferritin is a major determinant of lipid phenotype in familial combined hyperlipidemia and familial hypertriglyceridemia
    • Mateo-Gallego R, Calmarza P, Jarauta E, Burillo E, Cenarro A, Civeira F. Plasma ferritin is a major determinant of lipid phenotype in familial combined hyperlipidemia and familial hypertriglyceridemia. Metabolism 2010;59:154-8
    • (2010) Metabolism , vol.59 , pp. 154-158
    • Mateo-Gallego, R.1    Calmarza, P.2    Jarauta, E.3    Burillo, E.4    Cenarro, A.5    Civeira, F.6
  • 9
    • 56149091040 scopus 로고    scopus 로고
    • Hyperferritinemia is associated with insulin resistance and fatty liver in patients without iron overload
    • Brudevold R, Hole T, Hammerstrøm J. Hyperferritinemia is associated with insulin resistance and fatty liver in patients without iron overload. PLoS One 2008;3:3547
    • (2008) PLoS One , vol.3 , pp. 3547
    • Brudevold, R.1    Hole, T.2    Hammerstrøm, J.3
  • 10
    • 0032692722 scopus 로고    scopus 로고
    • Insulin resistance-associated hepatic iron overload
    • Mendler MH, Turlin B, Moirand R, et al. Insulin resistance-associated hepatic iron overload. Gastroenterology 1999;117:1155-63
    • (1999) Gastroenterology , vol.117 , pp. 1155-1163
    • Mendler, M.H.1    Turlin, B.2    Moirand, R.3
  • 13
    • 84860424165 scopus 로고    scopus 로고
    • Hereditary hyperferritinemia-cataract syndrome presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L-ferritin gene in a Swiss family
    • Rüfer A, Howell JP, Lange AP, et al. Hereditary hyperferritinemia-cataract syndrome presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L-ferritin gene in a Swiss family. Eur J Haematol 2011;87:274-8
    • (2011) Eur J Haematol , vol.87 , pp. 274-278
    • Rüfer, A.1    Howell, J.P.2    Lange, A.P.3
  • 14
    • 0344305685 scopus 로고    scopus 로고
    • Hereditary hyperferritinemia-cataract syndrome
    • Craig JE, Clark JB, McLeod J, et al. Hereditary hyperferritinemia-cataract syndrome. Arch Opthalmol 2003;121:1753-61
    • (2003) Arch Opthalmol , vol.121 , pp. 1753-1761
    • Craig, J.E.1    Clark, J.B.2    McLeod, J.3
  • 15
    • 0345275998 scopus 로고    scopus 로고
    • Hereditary hyperferritinemia-cataract syndrome and differential diagnosis of hereditary hemochromatosis
    • Sanders SJ, Suri M, Ross I. Hereditary hyperferritinemia-cataract syndrome and differential diagnosis of hereditary hemochromatosis. Postgrad Med J 2003;79:600-1
    • (2003) Postgrad Med J , vol.79 , pp. 600-601
    • Sanders, S.J.1    Suri, M.2    Ross, I.3
  • 18
    • 0031965464 scopus 로고    scopus 로고
    • Hereditary hyperferritinemia-cataract syndrome: two novel mutations in the L-ferritin iron-responsive element
    • Mumford AD, Vulliamy T, Lindsay J, Watson A. Hereditary hyperferritinemia-cataract syndrome: two novel mutations in the L-ferritin iron-responsive element. Blood 1998;91:367-8
    • (1998) Blood , vol.91 , pp. 367-368
    • Mumford, A.D.1    Vulliamy, T.2    Lindsay, J.3    Watson, A.4
  • 19
    • 14544267566 scopus 로고    scopus 로고
    • Role of ferritin and ferroportin genes in unexplained hyperferritinemia
    • Cazzola M. Role of ferritin and ferroportin genes in unexplained hyperferritinemia. Best Pract Res Clin Haematol 2005;18:251-63
    • (2005) Best Pract Res Clin Haematol , vol.18 , pp. 251-263
    • Cazzola, M.1
  • 20
    • 0037860450 scopus 로고    scopus 로고
    • Molecular analyses of patients with hyperferritinemia and normal plasma iron values reveal both L-ferritin IRE and 3 new ferroportin (slc11A3) mutations
    • Hetet G, Devaux I, Soufir N, Grandchamp B, Beaumont C. Molecular analyses of patients with hyperferritinemia and normal plasma iron values reveal both L-ferritin IRE and 3 new ferroportin (slc11A3) mutations. Blood 2003;102:1904-10
    • (2003) Blood , vol.102 , pp. 1904-1910
    • Hetet, G.1    Devaux, I.2    Soufir, N.3    Grandchamp, B.4    Beaumont, C.5
  • 21
    • 84872494726 scopus 로고    scopus 로고
    • Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation
    • Griffiths WJ, Mayr R, McFarlane I, et al. Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation. Transfusion 2010;50:1144-55
    • (2010) Transfusion , vol.50 , pp. 1144-1155
    • Griffiths, W.J.1    Mayr, R.2    McFarlane, I.3
  • 22
    • 79959258419 scopus 로고    scopus 로고
    • Secondary hemophagocytic syndrome in adults: a case series of 18 patients in a single institution and a review of literature
    • Shabbir M, Lucas J, Lazarchick J, Shirai K. Secondary hemophagocytic syndrome in adults: a case series of 18 patients in a single institution and a review of literature. Hematol Oncol 2011;29:100-6
    • (2011) Hematol Oncol , vol.29 , pp. 100-106
    • Shabbir, M.1    Lucas, J.2    Lazarchick, J.3    Shirai, K.4
  • 24
    • 79956130019 scopus 로고    scopus 로고
    • Unusually high ferritin in a patient with obstructive jaundice
    • Sami SS, Penston J, Hiang LT, Barlow I. Unusually high ferritin in a patient with obstructive jaundice. Ann Clin Biochem 2011;48:272-5
    • (2011) Ann Clin Biochem , vol.48 , pp. 272-275
    • Sami, S.S.1    Penston, J.2    Hiang, L.T.3    Barlow, I.4
  • 25
    • 85084724525 scopus 로고    scopus 로고
    • Plasma ferritin in acute hepatocellular damage
    • Chotoo IB, Stephen F, John J, John PB. Plasma ferritin in acute hepatocellular damage. Clin Chem 2000;46:885-6
    • (2000) Clin Chem , vol.46 , pp. 885-886
    • Chotoo, I.B.1    Stephen, F.2    John, J.3    John, P.B.4
  • 26
    • 83155168445 scopus 로고    scopus 로고
    • Acute liver failure caused by drug-induced hypersensitivity syndrome associated with hyperferritinemia
    • Miyazaki M, Tanaka M, Ueda A, et al. Acute liver failure caused by drug-induced hypersensitivity syndrome associated with hyperferritinemia. World J Gastroenterol 2011;17:4928-31
    • (2011) World J Gastroenterol , vol.17 , pp. 4928-4931
    • Miyazaki, M.1    Tanaka, M.2    Ueda, A.3
  • 27
  • 28
    • 43949133012 scopus 로고    scopus 로고
    • Low glycosylated ferritin, a good marker for the diagnosis of hemophagocytic syndrome
    • Fardet L, Coppo P, Kettaneh A, Dehoux M, Cabane J, Lambotte O. Low glycosylated ferritin, a good marker for the diagnosis of hemophagocytic syndrome. Arthritis Rheum 2008;58:1521-7
    • (2008) Arthritis Rheum , vol.58 , pp. 1521-1527
    • Fardet, L.1    Coppo, P.2    Kettaneh, A.3    Dehoux, M.4    Cabane, J.5    Lambotte, O.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.