Hepcidin levels in Diamond-Blackfan anemia reflect
erythropoietic activity and transfusion dependency

J 2014

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency

POSPÍŠILOVÁ, Dagmar, D. HOLUB, Z. ZIDOVA, L. SULOVSKA, J. HOUDA et. al.

Základní údaje

Originální název

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency

Autoři

POSPÍŠILOVÁ, Dagmar (203 Česká republika), D. HOLUB (203 Česká republika), Z. ZIDOVA (203 Česká republika), L. SULOVSKA (203 Česká republika), J. HOUDA (203 Česká republika), V. MIHAL (203 Česká republika), I. HADACOVA (203 Česká republika), Lenka RADOVÁ (203 Česká republika, garant, domácí), P. DZUBAK (203 Česká republika), Marian HAJDÚCH (203 Česká republika), Vladimír DIVOKÝ (203 Česká republika) a M. HORVATHOVA (203 Česká republika)

Vydání

Haematologica, PAVIA, FERRATA STORTI FOUNDATION, 2014, 0390-6078

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30200 3.2 Clinical medicine

Stát vydavatele

Itálie

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 5.814

Kód RIV

RIV/00216224:14740/14:00078458

Organizační jednotka

Středoevropský technologický institut

DOI

http://dx.doi.org/10.3324/haematol.2014.104034

UT WoS

000342833500008

Klíčová slova anglicky

Diamond Blackfan anemia; hepcidin levels; erythropoietic activity; transfusion dependency

Štítky

kontrola MP, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 6. 3. 2015 09:04, Martina Prášilová

Anotace

V originále

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.

Návaznosti

306242, interní kód MU

Název: NGS-PTL - Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia (Akronym: NGS-PTL)

Investor: Evropská unie, NGS-PTL - Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia, Spolupráce

Citovat

POSPÍŠILOVÁ, Dagmar, D. HOLUB, Z. ZIDOVA, L. SULOVSKA, J. HOUDA, V. MIHAL, I. HADACOVA, Lenka RADOVÁ, P. DZUBAK, Marian HAJDÚCH, Vladimír DIVOKÝ a M. HORVATHOVA. Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency. Haematologica. PAVIA: FERRATA STORTI FOUNDATION, 2014, roč. 99, č. 7, s. 118-121. ISSN 0390-6078. Dostupné z: https://dx.doi.org/10.3324/haematol.2014.104034.

@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 a M. HORVATHOVA. Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency. \textit{Haematologica}. PAVIA: FERRATA STORTI FOUNDATION, 2014, roč.~99, č.~7, s.~118-121. ISSN~0390-6078. Dostupné z: https://dx.doi.org/10.3324/haematol.2014.104034.

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