Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Paraplegia and SPG3A[original query] |
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| Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia. Archives of neurology 2006 May 63 (5): 750-5. Crippa Francesca, Panzeri Chris, Martinuzzi Andrea, Arnoldi Alessia, Redaelli Francesca, Tonelli Alessandra, Baschirotto Cinzia, Vazza Giovanni, Mostacciuolo Maria Luisa, Daga Andrea, Orso Genny, Profice Paolo, Trabacca Antonio, D'Angelo Maria Grazia, Comi Giacomo Pietro, Galbiati Sara, Lamperti Costanza, Bonato Sara, Pandolfo Massimo, Meola Giovanni, Musumeci Olimpia, Toscano Antonio, Trevisan Carlo Pietro, Bresolin Nereo, Bassi Maria Tere |
| Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31). BMC medical genetics 2008 9 (1): 71. Schlang Katharina J, Arning Larissa, Epplen Joerg T, Stemmler Susan |
| Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia. BMC neurology 2010 10 (1): 89. Alvarez Victoria, Sánchez-Ferrero Elena, Beetz Christian, Díaz Marta, Alonso Belén, Corao Ana I, Gámez Josep, Esteban Jesús, Gonzalo Juan F, Pascual-Pascual Samuel I, López de Munain Adolfo, Moris Germán, Ribacoba Renne, Márquez Celedonio, Rosell Jordi, Marín Rosario, García-Barcina Maria J, Del Castillo Emilia, Benito Carmen, Coto Eliecer, |
| Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia. Journal of neurology 2012 Feb 259 (2): 246-50. Sánchez-Ferrero Elena, Coto Eliecer, Corao Ana I, Díaz Marta, Gámez Josep, Esteban Jesús, Gonzalo Juan F, Pascual-Pascual Samuel I, López De Munaín Adolfo, Morís Germán, Infante Jon, Del Castillo Emilia, Márquez Celedonio, Alvarez Victor |
| A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings. Journal of neurology 2016 Jun . Polymeris Alexandros A, Tessa Alessandra, Anagnostopoulou Katherine, Rubegni Anna, Galatolo Daniele, Dinopoulos Argirios, Gika Artemis D, Youroukos Sotiris, Skouteli Eleni, Santorelli Filippo M, Pons Ros |
| JASPAC: Japan Spastic Paraplegia Research Consortium. Brain sciences 2018 8 8 (8): . Koh Kishin, Ishiura Hiroyuki, Tsuji Shoji, Takiyama Yoshihi |
| Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China. Molecular neurodegeneration 2018 07 13 (1): 36. Dong En-Lin, Wang Chong, Wu Shuang, Lu Ying-Qian, Lin Xiao-Hong, Su Hui-Zhen, Zhao Miao, He Jin, Ma Li-Xiang, Wang Ning, Chen Wan-Jin, Lin Xia |
| Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia. Scientific reports 2019 Oct 9 (1): 14412. Kadnikova V A, Rudenskaya G E, Stepanova A A, Sermyagina I G, Ryzhkova O |
| SPG3A gene polymorphisms in hereditary spastic paraplegia. International journal of clinical and experimental pathology 2020 1 10 (9): 9760-9764. Li Tian, Tu Li, Zhang Qian, Gu Ran, Wang Qian, Wang Bingjin, Yao Huan, Qu Xiang, Wang Wenqin, Tian Jinyo |
| Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan. Parkinsonism & related disorders 2021 5 87 87-91. Hsu Shao-Lun, Hsueh Hsueh-Wen, Chen Shih-Ying, Chang Yung-Yee, Tan Shennie, Hong Chien-Tai, Tsai Yu-Shuen, Yu Kai-Wei, Wu Hsiu-Mei, Liao Yi-Chu, Soong Bing-Wen, Hu Chaur-Jong, Lan Min-Yu, Lee Yi-Chu |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 11, 2023
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