| POSPÍŠILOVÁ, Dagmar, D. HOLUB, Z. ZIDOVA, L. SULOVSKA, J. HOUDA, V. MIHAL, I. HADACOVA, Lenka RADOVÁ, P. DZUBAK, Marian HAJDÚCH, Vladimír DIVOKÝ and M. HORVATHOVA. Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency. Haematologica. PAVIA: FERRATA STORTI FOUNDATION, 2014, vol. 99, No 7, p. 118-121. ISSN 0390-6078. Available from: https://dx.doi.org/10.3324/haematol.2014.104034. |
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@article{1217008,
author = {Pospíšilová, Dagmar and Holub, D. and Zidova, Z. and Sulovska, L. and Houda, J. and Mihal, V. and Hadacova, I. and Radová, Lenka and Dzubak, P. and Hajdúch, Marian and Divoký, Vladimír and Horvathova, M.},
article_location = {PAVIA},
article_number = {7},
doi = {http://dx.doi.org/10.3324/haematol.2014.104034},
keywords = {Diamond Blackfan anemia; hepcidin levels; erythropoietic activity; transfusion dependency},
language = {eng},
issn = {0390-6078},
journal = {Haematologica},
title = {Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency},
url = {http://www.haematologica.org/content/haematol/99/7/e118.full.pdf},
volume = {99},
year = {2014}
}
TY - JOUR
ID - 1217008
AU - Pospíšilová, Dagmar - Holub, D. - Zidova, Z. - Sulovska, L. - Houda, J. - Mihal, V. - Hadacova, I. - Radová, Lenka - Dzubak, P. - Hajdúch, Marian - Divoký, Vladimír - Horvathova, M.
PY - 2014
TI - Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency
JF - Haematologica
VL - 99
IS - 7
SP - 118-121
EP - 118-121
PB - FERRATA STORTI FOUNDATION
SN - 03906078
KW - Diamond Blackfan anemia
KW - hepcidin levels
KW - erythropoietic activity
KW - transfusion dependency
UR - http://www.haematologica.org/content/haematol/99/7/e118.full.pdf
L2 - http://www.haematologica.org/content/haematol/99/7/e118.full.pdf
N2 - Diamond-Blackfan anemia (DBA) is a rare congenital red cell aplasia associated with mutations in ribosomal proteins (RP) in 49-71% of cases.1 DBA is a clinically heterogeneous disorder with one-third of patients developing transfusion-acquired iron overload.2 The severity of anemia and transfusion dependency in DBA is comparable to transfusiondependent beta-thalassemia major; however, moderate to severe suppression of erythropoiesis in DBA2 is in contrast to accelerated ineffective erythropoiesis in beta-thalassemia.3,4 The knowledge of systemic iron regulation in DBA is limited.
ER -
POSPÍŠILOVÁ, Dagmar, D. HOLUB, Z. ZIDOVA, L. SULOVSKA, J. HOUDA, V. MIHAL, I. HADACOVA, Lenka RADOVÁ, P. DZUBAK, Marian HAJDÚCH, Vladimír DIVOKÝ and M. HORVATHOVA. Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency. \textit{Haematologica}. PAVIA: FERRATA STORTI FOUNDATION, 2014, vol.~99, No~7, p.~118-121. ISSN~0390-6078. Available from: https://dx.doi.org/10.3324/haematol.2014.104034.
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