Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic-Reference-Cited by-同舟云学术

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Phenotypical variability in congenital FVII deficiency follows the ISTH-SSC severity classification guidelines: a review with illustrative examples from the clinic

Published:2018-11 Issue: Volume:Volume 9 Page:211-218
ISSN:1179-2736
Container-title:Journal of Blood Medicine
language:en
Short-container-title:JBM

Author:

Jain Shilpa,Donkin Jennifer,Frey Mary Jane^ORCID,Peltier Skye^ORCID,Gunawardena Sriya,Cooper David L^ORCID

Publisher

Informa UK Limited

Subject

Hematology

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary coagulation factor VII deficiency caused by novel compound heterozygous mutations c.572-1G>A and c.1037A>C in a Chinese pedigree;Gene;2024-11

2. Anesthetic management with labor epidural analgesia of the parturient with severe factor VII deficiency: a case report;Regional Anesthesia & Pain Medicine;2024-06-30

3. Perioperative ROTEM® evaluation in a patient affected by severe VII factor deficiency undergoing microvascular decompression craniotomy for hemifacial spasm;Journal of Clinical Monitoring and Computing;2024-06-08

4. Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect;Haemophilia;2022-12-26

5. Novel heterozygous F7 gene mutation (c. C1286T) associated with congenital factor VII deficiency: A case report and literature review;Journal of Clinical Laboratory Analysis;2022-03-29

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