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	121.	SPAST mutations in Australian patients with hereditary spastic paraplegia. [electronic resource] by Vandebona, H Kerr, N P Liang, C Sue, C M Producer: 20130617 In: Internal medicine journal vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	122.	Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia. [electronic resource] by Chelban, Viorica Lynch, David S Houlden, Henry Wood, Nick Producer: 20170405 In: Journal of neurology vol. 263 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	123.	High diagnostic yield and novel variants in very late-onset spasticity. [electronic resource] by Almomen, Momen Martens, Kristina Quadir, Asfia Pontifex, Carly Sabine Hanson, Alexandra Korngut, Lawrence Pfeffer, Gerald Producer: 20200622 In: Journal of neurogenetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	124.	A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study. [electronic resource] by Namekawa, M Takiyama, Y Sakoe, K Shimazaki, H Amaike, M Niijima, K Nakano, I Nishizawa, M Producer: 20010621 In: Journal of the neurological sciences vol. 185 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	125.	Novel mutation of the Spastin gene in familial spastic paraplegia. [electronic resource] by De Bantel, A McWilliams, S Auysh, D Echol, C Sambuughin, N Sivakumar, K Producer: 20010726 In: Clinical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	126.	Spastin mutations in sporadic adult-onset upper motor neuron syndromes. [electronic resource] by Brugman, Frans Wokke, John H J Scheffer, Hans Versteeg, Martina H A Sistermans, Erik A van den Berg, Leonard H Producer: 20060131 In: Annals of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	127.	[Classification of hereditary spastic paraplegia (HSP)]. [electronic resource] by Utsumi, Hiroya Yuasa, Tatsuhiko Producer: 20031128 In: No to shinkei = Brain and nerve vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	128.	An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion. [electronic resource] by Beetz, Christian Nygren, Anders O H Deufel, Thomas Reid, Evan Producer: 20080403 In: Neurogenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	129.	A polymorphic Alu insertion that mediates distinct disease-associated deletions. [electronic resource] by Jahic, Amir Erichsen, Anne K Deufel, Thomas Tallaksen, Chantal M Beetz, Christian Producer: 20170726 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	130.	Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals. [electronic resource] by Sulek, Anna Elert, Ewelina Rajkiewicz, Marta Zdzienicka, Elzbieta Stepniak, Iwona Krysa, Wioletta Zaremba, Jacek Producer: 20130723 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	131.	'When atlastin meets spastin'. [electronic resource] by Di Fabio, R Tessa, A Marcotulli, C Leonardi, L Pierelli, F Santorelli, F M Casali, C Producer: 20150618 In: Clinical genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	132.	Amyloid-β oligomers induce synaptic damage via Tau-dependent microtubule severing by TTLL6 and spastin. [electronic resource] by Zempel, Hans Luedtke, Julia Kumar, Yatender Biernat, Jacek Dawson, Hana Mandelkow, Eckhard Mandelkow, Eva-Maria Producer: 20140121 In: The EMBO journal vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	133.	Identification of a novel mutation in the spastin gene (SPG4) in an Italian family with hereditary spastic paresis. [electronic resource] by Bertelli, M Cecchin, S Lorusso, L Sidoti, V Fabbri, A Lapucci, C Buda, A Pandolfo, M Producer: 20070313 In: Panminerva medica vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	134.	Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias. [electronic resource] by Reid, E Producer: 20030310 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	135.	Autosomal dominant hereditary spastic paraplegia: report of a large Italian family with R581X spastin mutation. [electronic resource] by Aridon, P Ragonese, P De Fusco, M Lo Coco, D Salemi, G Casari, G Savettieri, G Producer: 20071128 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	136.	The prevalence of hereditary spastic paraplegia and the occurrence of SPG4 mutations in Estonia. [electronic resource] by Braschinsky, Mark Luus, Siiri-Merike Gross-Paju, Katrin Haldre, Sulev Producer: 20091207 In: Neuroepidemiology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	137.	[Hereditary spastic paraplegia type 4 (SPG4): clinical and molecular-genetic characteristics]. [electronic resource] by Rudenskaia, G E Sermiagina, I G Illarioshkin, S N Sidorova, O P Fedotov, V P Poliakov, A V Producer: 20101220 In: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol. 110 Availability: No items available. Save to lists Add to cart (remove)
	138.	Identification of the Drosophila melanogaster homolog of the human spastin gene. [electronic resource] by Kammermeier, Lars Spring, Jürg Stierwald, Michael Burgunder, Jean-Marc Reichert, Heinrich Producer: 20040528 In: Development genes and evolution vol. 213 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	139.	An Automated Image Analysis System to Quantify Endosomal Tubulation. [electronic resource] by Newton, Timothy M Reid, Evan Producer: 20170718 In: PloS one vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	140.	Molecular basis of inherited spastic paraplegias. [electronic resource] by Casari, G Rugarli, E Producer: 20011101 In: Current opinion in genetics & development vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 343 results.