Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Hypertension and NOTCH3[original query] |
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Cerebral microbleeds in CADASIL: a gradient-echo magnetic resonance imaging and autopsy study. Stroke 2002 1 33 (1): 67-71. Dichgans Martin, Holtmannspötter Markus, Herzog Jürgen, Peters Nils, Bergmann Michael, Yousry Tarek |
Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese. Journal of neurology 2009 Feb 256 (2): 249-55. Lee Yi-Chung, Liu Chin-San, Chang Ming-Hong, Lin Kon-Ping, Fuh Jong-Ling, Lu Yi-Chu, Liu Ya-Fen, Soong Bing-W |
Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals. Stroke; a journal of cerebral circulation 2010 Apr 41 (4): 630-4. Adib-Samii Poneh, Brice Glen, Martin Roswell J, Markus Hugh |
Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease. Brain : a journal of neurology 2011 Nov 134 (Pt 11): 3384-97. Schmidt Helena, Zeginigg Marion, Wiltgen Marco, Freudenberger Paul, Petrovic Katja, Cavalieri Margherita, Gider Pierre, Enzinger Christian, Fornage Myriam, Debette Stephanie, Rotter Jerome I, Ikram Mohammad A, Launer Lenore J, Schmidt Reinhold, |
Mutations of NOTCH3 in childhood pulmonary arterial hypertension. Molecular genetics & genomic medicine 2014 May 2 (3): 229-39. Chida Ayako, Shintani Masaki, Matsushita Yoshihisa, Sato Hiroki, Eitoku Takahiro, Nakayama Tomotaka, Furutani Yoshiyuki, Hayama Emiko, Kawamura Yoichi, Inai Kei, Ohtsuki Shinichi, Saji Tsutomu, Nonoyama Shigeaki, Nakanishi Tosh |
Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Stroke; a journal of cerebral circulation 2015 Jun 46 (6): 1482-7. Rutten-Jacobs Loes C A, Traylor Matthew, Adib-Samii Poneh, Thijs Vincent, Sudlow Cathie, Rothwell Peter M, Boncoraglio Giorgio, Dichgans Martin, Bevan Steve, Meschia James, Levi Christopher, Rost Natalia S, Rosand Jonathan, Hassan Ahamad, Markus Hugh |
Association of Notch3 single-nucleotide polymorphisms and lacunar infarctions in patients. Experimental and therapeutic medicine 2016 Jan 11 (1): 28-32. Li Ying, Liu Nan, Chen Hui, Huang Yonghua, Zhang Weiw |
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
Effect of gene-gene and gene-environment interaction on the risk of first-ever stroke and poststroke death. Molecular genetics & genomic medicine 2019 Jul e846. Feng Congrui, Yang Yunyun, Yang Shujun, Tu Xin, Wang Yibo, Song Yiqing, Hui Rutai, Zhang Wei |
Genotypes and Phenotypes of Chinese Pediatric Patients With Idiopathic and Heritable Pulmonary Arterial Hypertension-A Single-Center Study. The Canadian journal of cardiology 2019 12 35 (12): 1851-1856. Zhang Hong-Sheng, Liu Qian, Piao Chun-Mei, Zhu Yan, Li Qiang-Qiang, Du Jie, Gu Ho |
Prevalence and Atypical Clinical Characteristics of NOTCH3 Mutations Among Patients Admitted for Acute Lacunar Infarctions. Frontiers in aging neuroscience 2020 6 12 130. Okada Takashi, Washida Kazuo, Irie Kenichi, Saito Satoshi, Noguchi Michio, Tomita Tsutomu, Koga Masatoshi, Toyoda Kazunori, Okazaki Shuhei, Koizumi Takashi, Mizuta Ikuko, Mizuno Toshiki, Ihara Masafu |
Genotype-phenotype correlations and effect of mutation location in Japanese CADASIL patients. Journal of human genetics 2020 4 65 (8): 637-646. Mukai Mao, Mizuta Ikuko, Watanabe-Hosomi Akiko, Koizumi Takashi, Matsuura Jun, Hamano Ai, Tomimoto Hidekazu, Mizuno Toshi |
Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report. BMC neurology 2020 3 20 (1): 72. He Ruojie, Li Huan, Sun Yiming, Chen Menglong, Wang Liang, Zhu Yuling, Zhang Che |
Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study. Jornal de pediatria 2021 Oct . Nakwan Narongsak, Mahasirimongkol Surakameth, Satproedprai Nusara, Chaiyasung Tassamonwan, Kunhapan Punna, Charoenlap Cheep, Singkhamanan Kamonnut, Charalsawadi Chariyaw |
Effect of NOTCH3 EGFr Group, Sex, and Cardiovascular Risk Factors on CADASIL Clinical and Neuroimaging Outcomes. Stroke 2022 7 53 (10): 3133-3144. Hack Remco J, Cerfontaine Minne N, Gravesteijn Gido, Tap Stephan, Hafkemeijer Anne, van der Grond Jeroen, Witjes-Ané Marie-Noëlle, Baas Frank, Rutten Julie W, Lesnik Oberstein Saskia A |
Whole Exome Sequencing of Patients With Heritable and Idiopathic Pulmonary Arterial Hypertension in Central Taiwan. Frontiers in cardiovascular medicine 2022 9 911649. Liang Kae-Woei, Chang Sheng-Kai, Chen Yu-Wei, Lin Wei-Wen, Tsai Wan-Jane, Wang Kuo-Ya |
High frequency of HTRA1 AND ABCC6 mutations in Japanese patients with adult-onset cerebral small vessel disease. Journal of neurology, neurosurgery, and psychiatry 2022 10 94 (1): 74-81. Uemura Masahiro, Hatano Yuya, Nozaki Hiroaki, Ando Shoichiro, Kondo Hajime, Hanazono Akira, Iwanaga Akira, Murota Hiroyuki, Osakada Yosuke, Osaki Masato, Kanazawa Masato, Kanai Mitsuyasu, Shibata Yoko, Saika Reiko, Miyatake Tadashi, Aizawa Hitoshi, Ikeuchi Takeshi, Tomimoto Hidekazu, Mizuta Ikuko, Mizuno Toshiki, Ishihara Tomohiko, Onodera Osa |
Modifiable Vascular Risk Factors Contribute to Stroke in 1,080 NOTCH3 R544C Carriers in Taiwan Biobank. International journal of stroke : official journal of the International Stroke Society 2023 7 17474930231191991. Hung-Jen Lin, Chih-Hao Chen, Ming-Wei Su, Chien-Wei Lin, Yu-Wen Cheng, Sung-Chun Tang, Jiann-Shing Je |
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