Human Genome Epidemiology Literature Finder
|
Records 1 - 6 (of 6 Records) |
| Query Trace: Stroke and SERPINC1[original query] |
|---|
| Genetic variants of connexin37 are associated with carotid intima-medial thickness and future onset of ischemic stroke. Atherosclerosis 2011 Jan 214 (1): 101-6. Leu Hsin-Bang, Chung Chia-Min, Chuang Shao-Yuan, Bai Chyi-Huey, Chen Jiunn-Rong, Chen Jaw-Wen, Pan Wen-Ha |
| Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture. Journal of thrombosis and haemostasis : JTH 2013 Aug . Puurunen M, Salo P, Engelbarth S, Javela K, Perola M |
| Genotype phenotype correlation in a pediatric population with antithrombin deficiency. European journal of pediatrics 2019 7 178 (10): 1471-1478. Kovac Mirjana, Mitic Gorana, Djilas Iva, Kuzmanovic Milos, Serbic Olivera, Lekovic Danijela, Tomic Branko, Bereczky Zsuzsan |
| Genetic modifiers of long-term survival in sickle cell anemia. Clinical and translational medicine 2020 Aug 10 (4): e152. Wonkam Ambroise, Chimusa Emile R, Mnika Khuthala, Pule Gift Dineo, Ngo Bitoungui Valentina Josiane, Mulder Nicola, Shriner Daniel, Rotimi Charles N, Adeyemo Adebowa |
| Utility of the SERPINC1 Gene Test in Ischemic Stroke Patients With Antithrombin Deficiency. Frontiers in neurology 2022 6 13 841934. Kim Seondeuk, Lee Woo-Jin, Moon Jangsup, Jung Keun-H |
| Cryptogenic Stroke in the Young: Role of Candidate Gene Polymorphisms in Indian Patients with Ischemic Etiology. Neurology India 2022 1 69 (6): 1655-1662. Salomi Bodda S B, Solomon Raja, Turaka Vijay Prakash, Aaron Sanjith, Christudass Christhunesa |
- Page last reviewed:Feb 1, 2024
- Content source: