Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Pathogenesis study of inherited dysfibrinogenemia].

Zhonghua yi xue za zhi - 18 Mar 2014

Liao Zhaoping, Xu Siqi, Tang Huqiang, Xie Yiyi, Duan Xiuzhi, Liu Chunhua, Cheng Yue, Chen Yuhua, Wang Deqiang, Luo Miao, Tao Zhihua

Abstract excerpt

OBJECTIVE: To explore the pathogenesis of a family with inherited dysfibrinogenemia. METHODS: Coagulation parameters of peripheral venous blood of a family with inherited dysfibrinogenemia from November 2012 were measured. And platelet and fibrinogen functions were examined by thromboelastogram. The antigen concentration of fibrinogen was detected by immune nephelometry. All exons and exon-intron boundaries of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Afibrinogenemia
Share to Fibrinogens, Abnormal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Heterozygote

Share to Homozygote

Share to Mutation

Share to Pedigree

Share to Phenotype

Source

Identifiers

PMID: 24844956

Genes

FGG
FGA
FGB
SDS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Pathogenesis study of inherited dysfibrinogenemia].PMID 24844956Read ↗

[A Family with Congenital Dysfibrinogenemia and Blood Transfusion].Semantic proximity Read ↗

[Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].Semantic proximity Read ↗

[Congenital Fibrinogen Deficiency Caused by Novel FGG Gene Mutation].Semantic proximity Read ↗

[Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A variant of the FGB gene].Semantic proximity Read ↗

[Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia].Semantic proximity Read ↗

[Phenotype and genotype analyses of two pedigrees with inherited fibrinogen deficiency].Semantic proximity Read ↗

[Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency].Semantic proximity Read ↗

Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.Semantic proximity Read ↗

Human Fibrinogen: Molecular and Genetic Aspects of Congenital DisordersSemantic proximity Read ↗

[Pedigree Analysis and Diagnosis of Congenital Dysfibrinogenemia: A Case Report].Semantic proximity Read ↗

[Research progress on hereditary fibrinogen abnormalities].Semantic proximity Read ↗

Clinical and molecular characterization of Iranian patients with congenital fibrinogen disorders.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.