Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 30 Records) |
Query Trace: Stroke and GLA[original query] |
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Apolipoprotein E genotype, coagulation, and survival following acute stroke. Neurology 2001 Sep 57 (6): 1097-100. Weir C J, McCarron M O, Muir K W, Dyker A G, Bone I, Lees K R, Nicoll J |
Lack of association between the C3435T polymorphism in the human multidrug resistance (MDR1) gene and response to antiepileptic drug treatment. Epilepsia 2005 May 46 (5): 643-7. Sills Graeme J, Mohanraj Rajiv, Butler Elaine, McCrindle Sheila, Collier Lindsay, Wilson Elaine A, Brodie Martin |
Functional promoter polymorphism in the VKORC1 gene is no major genetic determinant for coronary heart disease in Northern Germans. Thrombosis and haemostasis 2007 Jun 97 (6): 998-1002. Watzka Matthias, Nebel Almut, El Mokhtari Nour Eddine, Ivandic Boris, Müller Jens, Schreiber Stefan, Oldenburg Johann |
Mutations of the GLA gene in young patients with stroke: the PORTYSTROKE study--screening genetic conditions in Portuguese young stroke patients. Stroke; a journal of cerebral circulation 2010 Mar 41 (3): 431-6. Baptista Miguel Viana, Ferreira Susana, Pinho-E-Melo Teresa, Carvalho Marta, Cruz Vítor T, Carmona Cátia, Silva Fernando A, Tuna Assunção, Rodrigues Miguel, Ferreira Carla, Pinto Ana A N, Leitão André, Gabriel João Paulo, Calado Sofia, Oliveira João Paulo, Ferro José M, |
Higher frequency of paraoxonase gene polymorphism and cardiovascular impairment among Brazilian Fabry Disease patients. Clinical biochemistry 2012 Jul . Barris-Oliveira AC, Müller KB, Turaça LT, Pesquero JB, Martins AM, D'Almeida V |
[The polymorphism of matrix Gla-protein gene in ischemic atherothrombotic stroke patients]. Fiziolohichny? zhurnal (Kiev, Ukraine : 1994) 2012 58 (5): 14-21. Harbuzova V Iu, Matla? O I, Ataman Iu O, Dubovyk Ie I, Borodenko A O, Obukhova O A, Ataman O |
p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small-vessel occlusion in elderly Japanese males. European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 21 (1): 49-56. Nakamura K, Sekijima Y, Nakamura K, Hattori K, Nagamatsu K, Shimizu Y, Yazaki M, Sakurai A, Endo F, Fukushima Y, Ikeda S |
[Analysis of matrix Gla-protein (MGP) G-7A polymorphism association with ischemic atherothrombotic stroke in persons with risk factors]. T?Sitologii?a i genetika 0 47 (5): 33-40. Ataman O V, Polonikov O V, Harbuzova V Iu, Ataman Iu O, Matla? O |
An intronic haplotype in a galactosidase A is associated with reduced mRNA expression in males with cryptogenic stroke. Gene 2014 Oct 549 (2): 275-9. Zeevi David A, Hakam-Spector Elinor, Herskovitz Yair, Beeri Rachel, Elstein Deborah, Altarescu Gheo |
Prevalence of CADASIL and Fabry Disease in a Cohort of MRI Defined Younger Onset Lacunar Stroke. PloS one 2015 10 (8): e0136352. Kilarski Laura L, Rutten-Jacobs Loes C A, Bevan Steve, Baker Rob, Hassan Ahamad, Hughes Derralynn A, Markus Hugh S, |
[Association of allelic polymorphisms of genes matrix Gla-protein system with ischemic atherothrombotic stroke]. Fiziolohichny? zhurnal (Kiev, Ukraine : 1994) 2015 61 (1): 19-27. Garbuzova V Yu, Stroy D A, Dosenko V E, Dubovyk Ye I, Borodenko A O, Shimko K A, Obukhova O A, Ataman O |
The Modulatory Effects of the Polymorphisms in GLA 5'-Untranslated Region Upon Gene Expression Are Cell-Type Specific. JIMD reports 2015 23 27-34. Ferreira Susana, Reguenga Carlos, Oliveira João Pau |
[Prevalence of ischemic stroke in young adults and Fabry disease]. Zhonghua yi xue za zhi 2014 Dec 94 (47): 3717-20. Song Xiaowei, Xue Sufang, Fan Chunqiu, Li Xiaoying, Wu Ji |
Screening for Fabry's disease in young patients with ischemic stroke in a Chinese population. The International journal of neuroscience 2016 Mar 1-14. Song Xiaowei, Xue Sufang, Zhao Jingyan, Wu Ji |
Prevalence of Fabry disease and GLA c.196G>C variant in Japanese stroke patients. Journal of human genetics 2017 Mar . Nagamatsu Kiyoshiro, Sekijima Yoshiki, Nakamura Katsuya, Nakamura Kimitoshi, Hattori Kiyoko, Ota Masao, Shimizu Yusaku, Endo Fumio, Ikeda Shu-Ic |
Screening for Fabry Disease in Japanese Patients with Young-Onset Stroke by Measuring ?-Galactosidase A and Globotriaosylsphingosine. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2018 Sep . Kinoshita Naoto, Hosomi Naohisa, Matsushima Hayato, Nakamori Masahiro, Yagita Yoshiki, Yamawaki Takemori, Torii Tsuyoshi, Kitamura Takeshi, Sueda Yoshimasa, Shimomura Ryo, Araki Mutsuko, Nezu Tomohisa, Aoki Shiro, Ishii Satoshi, Maruyama Hiroki, Matsumoto Masayasu, Maruyama Hirofu |
Phenotype and biochemical heterogeneity in late onset Fabry disease defined by N215S mutation. PloS one 2018 4 13 (4): e0193550. Lavalle L, Thomas A S, Beaton B, Ebrahim H, Reed M, Ramaswami U, Elliott P, Mehta A B, Hughes D |
How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study. Neurology 2019 11 93 (22): e2007-e2020. Tan Rhea Y Y, Traylor Matthew, Megy Karyn, Duarte Daniel, Deevi Sri V V, Shamardina Olga, Mapeta Rutendo P, , Ouwehand Willem H, Gräf Stefan, Downes Kate, Markus Hugh |
Matrix Gla protein polymorphism rs1800801 associates with recurrence of ischemic stroke. PloS one 2020 6 15 (6): e0235122. Hendrix Philipp, Sofoluke Nelson, Adams Matthew, Kunaprayoon Saran, Zand Ramin, Kolinovsky Amy N, Person Thomas N, Gupta Mudit, Goren Oded, Kirchner H Lester, Schirmer Clemens M, Rost Natalia S, Faber James E, Griessenauer Christoph |
Cornea verticillata and acroparesthesia efficiently discriminate clusters of severity in Fabry disease. PloS one 2020 5 15 (5): e0233460. Mauhin Wladimir, Benveniste Olivier, Amelin Damien, Montagner Clémence, Lamari Foudil, Caillaud Catherine, Douillard Claire, Dussol Bertrand, Leguy-Seguin Vanessa, D'Halluin Pauline, Noel Esther, Zenone Thierry, Matignon Marie, Maillot François, Ly Kim-Heang, Besson Gérard, Willems Marjolaine, Labombarda Fabien, Masseau Agathe, Lavigne Christian, Lacombe Didier, Maillard Hélène, Lidove Olivi |
Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups. Stroke 2020 Feb STROKEAHA119028840. Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau |
Detailed Phenotype of GLA Variants Identified by the Nationwide Neurological Screening of Stroke Patients in the Czech Republic. Journal of clinical medicine 2021 8 10 (16): . Reková Petra, Dostálová Gabriela, Kemlink David, Paulasová Schwabová Jaroslava, Dubská Zora, Vaneckova Manuela, Mašek Martin, Kodet Ond?ej, Poup?tová Helena, Mazurová Stella, Rajdova Aneta, Vlckova Eva, Tábo?íková Alena, Fafejtová Št?pánka, Nevsimalova Miroslava, Linhart Aleš, Tomek Al |
Mutation analysis of the GLA gene in Chinese patients with intracerebral hemorrhage. Neurobiology of aging 2021 Feb . Tang Lu, Yang Qiong, Liu Xiaolu, Tian Danyang, Wu Chenying, Han Qi, Yan Xin, Ding Shengchao, Fan Dongshe |
Nationwide screening for Fabry disease in unselected stroke patients. PloS one 2021 12 16 (12): e0260601. Tomek Aleš, Petra Reková, Paulasová Schwabová Jaroslava, Olšerová Anna, Škor?a Miroslav, Nevšímalová Miroslava, Šim?nek Libor, Herzig Roman, Fafejtová Št?pánka, Mikulenka Petr, Tábo?íková Alena, Neumann Ji?í, Brzezny Richard, Sobolová Helena, Bartoník Jan, Václavík Daniel, Vachová Marta, Bechyn? Karel, Havlíková Hana, Prax Tomáš, Ša?ák Daniel, ?erníková Irena, Onde?ková Iva, Procházka Petr, Rajner Jan, Škoda Miroslav, Novák Jan, Škoda Ond?ej, Bar Michal, Mikulík Robert, Dostálová Gabriela, Linhart Aleš, |
Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients. Annals of neurology 2022 12 . Park Hong-Kyun, Lee Keon-Joo, Park Jong-Moo, Kang Kyusik, Lee Soo Joo, Kim Jae Guk, Cha Jae-Kwan, Kim Dae-Hyun, Han Moon-Ku, Kang Jihoon, Kim Beom Joon, Park Tai Hwan, Park Moo-Seok, Lee Kyung Bok, Lee Jun, Hong Keun-Sik, Cho Yong-Jin, Lee Byung-Chul, Yu Kyung-Ho, Oh Mi Sun, Kim Joon-Tae, Choi Kang-Ho, Kim Dong-Eog, Ryu Wi-Sun, Choi Jay Chol, Kwon Jee-Hyun, Kim Wook-Joo, Shin Dong-Ick, Sohn Sung Il, Hong Jeong-Ho, Lee Juneyoung, Lee Kyunghoon, Song Junghan, Bae Joon Seol, Cheong Hyun Sub, Debette Stéphanie, Bae Hee-Jo |
Exome-based gene panel analysis in a cohort of acute juvenile ischemic stroke patients:relevance of NOTCH3 and GLA variants. Journal of neurology 2022 11 . Härtl Johanna, Hartberger Julia, Wunderlich Silke, Cordts Isabell, Bafligil Cemsel, Sturm Marc, , Westphal Dominik, Haack Tobias, Hemmer Bernhard, Ikenberg Benno David, Deschauer Marc |
Phenotypes of undiagnosed adults with actionable OTC and GLA variants. HGG advances 2023 8 4 (4): 100226. Jessica I Gold, Sarina Madhavan, Joseph Park, Hana Zouk, Emma Perez, Alanna Strong, Theodore G Drivas, Amel Karaa, Marc Yudkoff, Daniel Rader, , , Robert C Green, Nina B Go |
Brain MRI correlations with disease burden and biomarkers in Fabry disease. Journal of neurology 2023 6 . Yawen Zhao, Ying Zhu, Fan Li, Yunchuang Sun, Wei Ma, Yuan Wu, Wei Zhang, Zhaoxia Wang, Yun Yuan, Yining Hua |
Late-onset fabry disease due to the p.Phe113Leu variant: the first italian cluster of five families. Metabolic brain disease 2023 4 . Vittoria Cianci, Angelo Pascarella, Lucia Manzo, Sara Gasparini, Oreste Marsico, Anna Mammì, Carmelo Massimiliano Rao, Claudio Franzutti, Umberto Aguglia, Edoardo Ferlaz |
Genotype-Phenotype Correlations in 293 Russian Patients with Causal Fabry Disease Variants. Genes 2023 11 14 (11): . Kirill Savostyanov, Alexander Pushkov, Ilya Zhanin, Natalya Mazanova, Alexander Pakhomov, Elena Trufanova, Alina Alexeeva, Dmitry Sladkov, Ludmila Kuzenkova, Aliy Asanov, Andrey Fisen |
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- Page last updated:Apr 22, 2024
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