Protein S Deficiency
What's New
Last Posted: Jun 25, 2024
- The genetic risk factors for cerebral venous thrombosis: a case-control study in a Chinese national comprehensive hospital.
Shaoying Wang, et al. Thrombosis journal 2024 0 (1) 50 - The risk profiles of pregnancy-related cerebral venous thrombosis: a retrospective study in a comprehensive hospital.
Shaoying Wang, et al. BMC neurology 2024 0 (1) 182 - Plasminogen Activator Inhibitor-1 4G/5G Promoter Polymorphism in Indian Patients with Deep Vein Thrombosis.
Saniya Sharma, et al. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2024 0 (2) 331-334 - Evaluation of acquired and hereditary risk factors for the development of thromboembolism in patients with systemic lupus erythematosus.
Vildan Gürsoy, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2023 0 - Endothelial dysfunction, thrombophilia, and nailfold capillaroscopic features in livedoid vasculopathy.
O Apti Sengun, et al. Microvascular research 2023 0 104591 - The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients.
Tereza Fenclova, et al. Research and practice in thrombosis and haemostasis 2023 0 (4) 100194 - Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies.
A Theron, et al. Frontiers in pediatrics 2023 0 1197795 - Thrombophilia screening in the routine clinical care of children with arterial ischemic stroke.
Kristin Maher et al. Pediatr Blood Cancer 2023 e30381 - Pregnancy, thrombophilia, and the risk of a first venous thrombosis: systematic review and bayesian meta-analysis.
Croles F Nanne, et al. BMJ (Clinical research ed.) 2017 0 j4452 - The prevalence and clinical manifestation of hereditary thrombophilia in Korean patients with unprovoked venous thromboembolisms.
Lee Su Yeon, et al. PloS one 2017 0 (10) e0185785
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Content source: