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	41.	There might be more to SPG4! [electronic resource] by van de Warrenburg, Bart P C Producer: 20090420 In: Journal of neurology, neurosurgery, and psychiatry vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	The C. elegans homologue of the spastic paraplegia protein, spastin, disassembles microtubules. [electronic resource] by Matsushita-Ishiodori, Yuka Yamanaka, Kunitoshi Ogura, Teru Producer: 20070809 In: Biochemical and biophysical research communications vol. 359 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia. [electronic resource] by Fink, John K Producer: 20081118 In: Neurology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Hereditary spastic paraplegia SPG4: what is known and not known about the disease. [electronic resource] by Solowska, Joanna M Baas, Peter W Producer: 20151116 In: Brain : a journal of neurology vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia. [electronic resource] by Svenson, Ingrid K Kloos, Mark T Jacon, Amy Gallione, Carol Horton, April C Pericak-Vance, Margaret A Ehlers, Michael D Marchuk, Douglas A Producer: 20060530 In: Neurogenetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Structure of spastin bound to a glutamate-rich peptide implies a hand-over-hand mechanism of substrate translocation. [electronic resource] by Han, Han Schubert, Heidi L McCullough, John Monroe, Nicole Purdy, Michael D Yeager, Mark Sundquist, Wesley I Hill, Christopher P Producer: 20200914 In: The Journal of biological chemistry vol. 295 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Hereditary spastic paraplegia masqueraded by congenital melanocytic nevus syndrome: Dual pathogenesis of germline non-mosaicism and somatic mosaicism. [electronic resource] by Sakaguchi, Yuri Uehara, Tomoko Sasaki, Marie Fujimura, Kimino Kishi, Kazuo Kosaki, Kenjiro Takenouchi, Toshiki Producer: 20201231 In: European journal of medical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Identification of a novel SPG4 tandem base substitution in a Chinese hereditary spastic paraplegia family. [electronic resource] by Zhao, Guohua Liu, Xiaomin Jiang, Peifang Producer: 20181015 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	A case report of a woman with young onset cognitive impairment associated with hereditary spastic paraplegia due to a mutation in the SPAST gene. [electronic resource] by Tisher, Annya Salardini, Arash Producer: 20170425 In: Journal of the neurological sciences vol. 367 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Spastin Interacts with CRMP5 to Promote Neurite Outgrowth by Controlling the Microtubule Dynamics. [electronic resource] by Ji, Zhisheng Zhang, Guowei Chen, Li Li, Jiong Yang, Yuhao Cha, Caihui Zhang, Jifeng Lin, Hongsheng Guo, Guoqing Producer: 20190521 In: Developmental neurobiology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients. [electronic resource] by Erfanian Omidvar, Maryam Torkamandi, Shahram Rezaei, Somaye Alipoor, Behnam Omrani, Mir Davood Darvish, Hossein Ghaedi, Hamid Producer: 20210618 In: Journal of neurology vol. 268 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey. [electronic resource] by Akçakaya, Nihan H Özeş Ak, Burçak Gonzalez, Michael A Züchner, Stefan Battaloğlu, Esra Parman, Yeşim Producer: 20200709 In: Neurologia i neurochirurgia polska vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Neuropathology: many paths lead to hereditary spastic paraplegia. [electronic resource] by Gould, Robert M Brady, Scott T Producer: 20050131 In: Current biology : CB vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Cell biology: nuclear dilemma resolved. [electronic resource] by Burke, Brian Producer: 20150702 In: Nature vol. 522 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	[Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia]. [electronic resource] by Akhmetgaleyeva, A F Khidiyatova, I M Saifullina, E V Idrisova, R F Magzhanov, R V Khusnutdinova, E K Producer: 20180205 In: Genetika vol. 52 Availability: No items available. Save to lists Add to cart (remove)
	56.	Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene. [electronic resource] by Proukakis, C Auer-Grumbach, M Wagner, K Wilkinson, P A Reid, E Patton, M A Warner, T T Crosby, A H Producer: 20030326 In: Human mutation vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	No correlation between amount of aberrant transcript and severity of phenotype in hereditary spastic paraplegia patients with a c.1242A > G splice mutation in the SPG4 gene. [electronic resource] by Sauter, Simone M Dörwald, Nadine Engel, Wolfgang Neesen, Jürgen Producer: 20061212 In: Journal of neurology vol. 253 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Four mutations of the spastin gene in Japanese families with spastic paraplegia. [electronic resource] by Basri, Rehana Yabe, Ichiro Soma, Hiroyuki Takei, Asako Nishimura, Hiroyuki Machino, Yuka Kokubo, Yasumasa Kosugi, Masafumi Okada, Ryuichirou Yukitake, Motohiro Tachibana, Hisao Kuroda, Yasuo Kuzuhara, Shigeki Sasaki, Hidenao Producer: 20061006 In: Journal of human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	A Japanese family with a novel nonsense mutation in the spastin gene associated with both cerebellar ataxia and cognitive impairment. [electronic resource] by Tsuchiya, Mai Koh, Kishin Ishida, Aki Ichinose, Yuta Shindo, Kazumasa Takiyama, Yoshihisa Producer: 20200225 In: Journal of the neurological sciences vol. 397 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	[Spastin gene mutation in Chinese patients with hereditary spastic paraplegia]. [electronic resource] by Zhao, Guo-hua Tang, Bei-sha Luo, Wei Xia, Kun Zhuang, Mao-you Kong, Fan-bin Yan, Xin-xiang Deng, Han-xiang Xiao, Jian-feng Xia, Jia-hui Producer: 20090225 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 20 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 343 results.