Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F10%3A6872" target="_blank" >RIV/00216208:11110/10:6872 - isvavai.cz</a>

Alternative codes found

RIV/00023736:_____/10:00008779 RIV/00216208:11130/10:6323 RIV/00843989:_____/10:00101625 RIV/00064203:_____/10:6323 RIV/00064165:_____/10:6872

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Dysfibrinogenemia in childhood: two cases of congenital dysfibrinogens

Original language description

A 2-year-old asymptomatic boy and his relatives were investigated for a suspected fibrinogen mutation after coagulation tests revealed a decreased functional fibrinogen level (family A). Eight-year-old and 1-year-old asymptomatic brothers were investigated for a suspected fibrinogen mutation after coagulation tests revealed a decreased functional fibrinogen level and prolonged thrombin time (family B). To identify whether genetic mutations were responsible for these dysfibrinogens, DNA extracted from the blood was analyzed.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

FD - Oncology and haematology

OECD FORD branch

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Project

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2010

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Blood coagulation & fibrinolysis

ISSN

0957-5235

e-ISSN

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Volume of the periodical

21

Issue of the periodical within the volume

7

Country of publishing house

US - UNITED STATES

Number of pages

9

Pages from-to

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UT code for WoS article

000282483500004

EID of the result in the Scopus database

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