Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 30 (of 115 Records) |
Query Trace: Protein S Deficiency[original query] |
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Prothrombotic genetic risk factors in patients with very early ST-segment elevation myocardial infarction. Journal of thrombosis and thrombolysis 2017 Jun . Rallidis Loukianos S, Gialeraki Argyri, Tsirebolos Georgios, Tsalavoutas Stylianos, Rallidi Maria, Iliodromitis Efstathi |
Non-genetic and genetic risk factors for adult cerebral venous thrombosis. Thrombosis research 2018 Jul 169 15-22. Green Mackenzie, Styles Toby, Russell Timothy, Sada Charif, Jallow Ebrima, Stewart Jack, Lazariashvili Otar, Lubomirova Irina, Cotlarciuc Ioana, Sharma Sapna, Han Thang S, Sharma Pank |
Diagnostic challenge of the newborn patients with heritable protein C deficiency. Journal of perinatology : official journal of the California Perinatal Association 2018 10 39 (2): 212-219. Ichiyama Masako, Inoue Hirosuke, Ochiai Masayuki, Ishimura Masataka, Shiraishi Akira, Fujiyoshi Junko, Yamashita Hironori, Sato Kazuo, Matsumoto Shinya, Hotta Taeko, Uchiumi Takeshi, Kang Dongchon, Ohga Shouic |
Risk factors for venous thromboembolism (VTE) recurrences in Thai patients without cancer. Hematology (Amsterdam, Netherlands) 2018 10 24 (1): 159-165. Satpanich Panchalee, Rojnuckarin Ponlap |
Inherited Thrombophilia and the Risk of Arterial Ischemic Stroke: A Systematic Review and Meta-Analysis. Journal of the American Heart Association 2019 9 8 (19): e012877. Chiasakul Thita, De Jesus Elizabeth, Tong Jiayi, Chen Yong, Crowther Mark, Garcia David, Chai-Adisaksopha Chatree, Messé Steven R, Cuker Ad |
Thrombophilic risk factors in hemodialysis: Association with early vascular access occlusion and patient survival in long-term follow-up. PloS one 2019 9 14 (9): e0222102. Grupp Clemens, Troche-Polzien Ilka, Stock Johanna, Bramlage Carsten, Müller Gerhard A, Koziolek Micha |
Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient. Journal of atherosclerosis and thrombosis 2019 5 27 (1): 100-103. Ueda Kazuki, Morishita Eriko, Shiraki Hironaga, Matsuoka Shunzo, Imashuku Shinsa |
[Exhaustive analysis of genetic mutations associated with protein S deficiency utilizing next-generation sequencing analysis]. [Rinsho ketsueki] The Japanese journal of clinical hematology 2019 5 60 (3): 171-183. Ichiki Akito, Inaba Hiroshi, Shinozawa Keiko, Amano Kagehiro, Fukutake Katsuyu |
Metabolomic Signature of Angiopoietin-Like Protein 3 Deficiency in Fasting and Postprandial State. Arteriosclerosis, thrombosis, and vascular biology 2019 Feb ATVBAHA118312021. Tikkanen Emmi, Minicocci Ilenia, Hällfors Jenni, Di Costanzo Alessia, D'Erasmo Laura, Poggiogalle Eleonora, Donini Lorenzo Maria, Würtz Peter, Jauhiainen Matti, Olkkonen Vesa M, Arca Marcel |
Pregnancy-related thrombosis risk in patients with protein C deficiency and comparison with pregnant women with heterozygous factor V Leiden mutation. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2019 12 31 (1): 55-59. Rugeri Lucia, Desage Stephanie, Khouatra Linda, Battie Catherine, Doret-Dion Muriel, Trzeciak Christine, Dargaud Yes |
Evaluation of etiology and pregnancy outcome in recurrent miscarriage patients. Saudi journal of biological sciences 2020 9 27 (10): 2809-2817. Ali Shafat, Majid Sabhiya, Niamat Ali Md, Taing Shahnaz, El-Serehy Hamed A, Al-Misned Fahad |
Genotype-Phenotype Relationships in a Large French Cohort of Subjects with Inherited Protein C Deficiency. Thrombosis and haemostasis 2020 7 120 (9): 1270-1281. Alhenc-Gelas Martine, Plu-Bureau Geneviève, Mauge Laetitia, Gandrille Sophie, Présot Isabelle, |
Two Novel Variants in the Protein S Gene PROS1 Are Associated with Protein S Deficiency and Thrombophilia. Acta haematologica 2020 7 144 (2): 222-226. Juhl David, Kuta Piotr, Shneyder Maria, Wünsche Falko, Nowak-Göttl Ulri |
Prothrombotic Factors Have Significant Association with Arterial and Venous Strokes in Indian Tamilians. The journal of applied laboratory medicine 2020 12 6 (1): 101-112. Narayan Sunil, Chandrasekaran Adithan, Basu Debdatta, Hanumanthappa Nandeesha, Aghoram Rajeswari, Dutta Tarun Kumar, Rejul Venugopal |
Potential protein-phenotype correlation in three lipopolysaccharide-responsive beige-like anchor protein-deficient patients. World journal of clinical cases 2021 8 9 (21): 5873-5888. Tang Wen-Juan, Hu Wen-Hui, Huang Ying, Wu Bing-Bing, Peng Xiao-Min, Zhai Xiao-Wen, Qian Xiao-Wen, Ye Zi-Qing, Xia Hai-Jiao, Wu Jie, Shi Jie- |
A study of hyperhomocysteinemia in cerebral venous sinus thrombosis. The Indian journal of medical research 2021 6 152 (6): 584-594. Kalita Jayantee, Singh Varun K, Misra Usha Ka |
Patent Foramen Ovale Closure among Patients with Hypercoagulable States Maintained on Antithrombotic Therapy. Cardiology 2021 2 146 (3): 375-383. Buber Jonathan, Guetta Victor, Orion David, Lubetsky Aharon, Borik Sharon, Vatury Ori, Israel Ari |
Genetic Variants in the Protein S ( PROS1 ) Gene and Protein S Deficiency in a Danish Population. TH open : companion journal to thrombosis and haemostasis 2021 11 5 (4): e479-e488. Larsen Ole Halfdan, Kjaergaard Alisa D, Hvas Anne-Mette, Nissen Peter |
Inherited and acquired thrombophilia in women of Indian ethnicity with recurrent pregnancy loss: An observational study from North India. Indian journal of pathology & microbiology 2021 10 64 (4): 741-745. Mishra Priyanka, Singh Kanwaljeet, Tyagi Seema, Juneja Richa, Mahapatra Manoranj |
Janus Kinase-2 Mutation Associated Portal Vein Thrombosis Complicating Liver Cirrhosis and Hepatocellular Carcinoma. Asian Pacific journal of cancer prevention : APJCP 2021 1 22 (1): 267-275. Rabie Hatem, Othman Warda, Elsabaawy Dalia M, Elshemy Eman E, Abdelmageed Neamat, Khalaf Fatma A, Bedair Hanan |
Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population. Frontiers in cardiovascular medicine 2021 8 796755. Wu Yingying, Liu Jingdi, Zeng Wei, Hu Bei, Hu Yu, Tang Liang |
Comprehensive Thrombophilia Evaluation in Cerebral Venous Thrombosis: A Single Center Cross Sectional Study. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 6 38 (3): 522-528. Kumar Rajiv, Vinny Pulikottil Wilson, Nair Vishnu G, Jakku Raje |
Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing. Diagnostics (Basel, Switzerland) 2022 5 12 (5): . Vrtel Petr, Slavik Ludek, Vodicka Radek, Stellmachova Julia, Prochazka Martin, Prochazkova Jana, Ulehlova Jana, Rohon Peter, Simurda Tomas, Stasko Jan, Martinkova Ivana, Vrtel Rad |
[Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2022 3 43 (1): 35-40. Xu Q Y, Yang L L, Xie H X, Jin Y H, Li X L, Zhou X X, Liu M N, Wang M |
PROS1 variant in sudden death case of pulmonary embolism caused by calcification in the inferior vena cava: The importance of postmortem genetic analysis. Legal medicine (Tokyo, Japan) 2022 2 55 102029. Miura Aya, Funayama Kazuhisa, Nyuzuki Hiromi, Takahashi Naoya, Yamamoto Takuma, Koyama Akihide, Ikeuchi Takeshi, Takatsuka Hisakazu, Nishio Haji |
Prevalence, Genetic Background, and Clinical Phenotype of Congenital Thrombophilia in Chronic Thromboembolic Pulmonary Hypertension. JACC. Asia 2022 11 2 (3): 247-255. Lian Tian-Yu, Liu Jian-Zhou, Guo Fan, Zhou Yu-Ping, Wu Tao, Wang Hui, Li Jing-Yi, Yan Xin-Xin, Peng Fu-Hua, Sun Kai, Xu Xi-Qi, Han Zhi-Yan, Jiang Xin, Wang Duo-Lao, Miao Qi, Jing Zhi-Che |
Evaluation of acquired and hereditary risk factors for the development of thromboembolism in patients with systemic lupus erythematosus. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2023 9 . Vildan Gürsoy, Sevil Sadri, Selime Ermur |
Endothelial dysfunction, thrombophilia, and nailfold capillaroscopic features in livedoid vasculopathy. Microvascular research 2023 8 150 104591. O Apti Sengun, T Ergun, T Guctekin, F Alibaz On |
The impact of PROS1 mutation position on thrombotic risk in protein S-deficient patients. Research and practice in thrombosis and haemostasis 2023 6 7 (4): 100194. Tereza Fenclova, Miloslava Matyskova, Dana Provaznikova, Frantisek Marecek, Vera Geierova, Zuzana Kovarova-Kudrnova, Ingrid Hrachovino |
Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies. Frontiers in pediatrics 2023 6 11 1197795. A Theron, S Ayadi, E Boissier, O Dautremay, J-F Schved, N Sirvent, I Diaz, G Captier, C Biron-Andreani, E Jeziors |
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- Page last updated:Apr 29, 2024
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