Heterozygous congenital Factor VII deficiency with the 9729del4 mutation, associated with severe spontaneous intracranial bleeding in an adolescent male-Reference-Cited by-同舟云学术

Heterozygous congenital Factor VII deficiency with the 9729del4 mutation, associated with severe spontaneous intracranial bleeding in an adolescent male

Published:2016-03 Issue: Volume:57 Page:8-12
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Cramer Thomas J.^ORCID,Anderson Kristin,Navaz Karanjia,Brown Justin M.,Mosnier Laurent O.,von Drygalski Annette

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference27 articles.

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3. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders;Peyvandi;J. Thromb. Haemost.,2012

4. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene;Herrmann;Haemophilia,2009

5. Twenty two novel mutations of the factor VII gene in factor VII deficiency;Wulff;Hum. Mutat.,2000

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1. Congenital Bleeding Disorders: Diagnosis and Management;Congenital Bleeding Disorders;2023

2. High Prevalence of Congenital Factor VII (FVII) Deficiency in Adolescent Females with Heavy Menstrual Bleeding and Iron Deficiency Anemia;Journal of Pediatric and Adolescent Gynecology;2022-12

3. Diagnosis and treatment discussion of congenital factor VII deficiency in pregnancy: A case report;World Journal of Clinical Cases;2021-07-26

4. Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic;Journal of Blood Medicine;2018-11

5. The future of bypassing agents for hemophilia with inhibitors in the era of novel agents;Journal of Thrombosis and Haemostasis;2018-10-11