Congenital disorders of glycosylation as an unusual cause of antithrombin deficiency and elevated thrombin generation-Reference-Cited by-同舟云学术

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Congenital disorders of glycosylation as an unusual cause of antithrombin deficiency and elevated thrombin generation

Published:2019-11-17 Issue:2 Volume:67 Page:
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Hasan Rida¹^ORCID,Kayani Saima²,Zia Ayesha¹^ORCID

Affiliation:

1. Division of Hematology/OncologyDepartment of PediatricsThe University of Texas Southwestern Medical Center Dallas Texas

2. Division of NeurologyDepartment of PediatricsThe University of Texas Southwestern Medical Center Dallas Texas

Funder

National Institutes of Health

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pbc.28069

Reference9 articles.

1. Thrombotic complications in patients with PMM2-CDG

2. Risk assessment of acute vascular events in congenital disorder of glycosylation type Ia

3. Multifactorial hypercoagulable state associated with a thrombotic phenotype in phosphomannomutase-2 congenital disorder of glycosylation (PMM2-CDG): Case report and brief review of the literature

4. The genetics of antithrombin

5. Elevated thrombin generation in patients with congenital disorder of glycosylation and combined coagulation factor deficiencies

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1. Comparative N ‐glycoproteomic analysis of Tibetan and lowland chicken fertilized eggs: Implications on proteins biofunction and species evolution;Journal of Food Biochemistry;2021-12-03

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