Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Paraplegia and ATL1[original query] |
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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, |
Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia. Journal of the neurological sciences 2015 Oct 357 (1-2): 167-72. Park Hyunwoong, Kang Seong-Ho, Park Seungman, Kim So Yeon, Seo Soo Hyun, Lee Seung Jun, Lee Jung Ae, Cho Sung Im, Sung Jung-Joon, Lee Kwang-Woo, Kim Ji Yeon, Park Sung Sup, Seong Moon-W |
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients. Journal of the neurological sciences 2015 Dec 359 (1-2): 35-9. Elert-Dobkowska Ewelina, Stepniak Iwona, Krysa Wioletta, Rajkiewicz Marta, Rakowicz Maria, Sobanska Anna, Rudzinska Monika, Wasielewska Anna, Pilch Jacek, Kubalska Jolanta, Lipczynska-Lojkowska Wanda, Kulczycki Jerzy, Kurdziel Katarzyna, Sikorska Agata, Beetz Christian, Zaremba Jacek, Sulek An |
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 |
Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients. Journal of molecular medicine (Berlin, Germany) 2018 6 96 (7): 701-712. Lu Cong, Li Li-Xi, Dong Hai-Lin, Wei Qiao, Liu Zhi-Jun, Ni Wang, Gitler Aaron D, Wu Zhi-Yi |
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 |
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 |
Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia. Frontiers in neurology 2022 5 13 872927. Shi Yuzhi, Wang An, Chen Bin, Wang Xingao, Niu Songtao, Li Wei, Li Shaowu, Zhang Zaiqia |
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia. Frontiers in neurology 2023 9 14 1239725. Amokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, Lindsay A Wilson, Jana Vandrovcova, Mary M Reilly, Christopher J Record, Michael Benatar, Gang Wu, Sharika Raga, Jo M Wilmshurst, Kireshnee Naidu, Michael Hanna, Melissa Nel, Jeannine M Heckma |
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- Page last updated:Mar 25, 2024
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