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	101.	FXYD1, a modulator of Na,K-ATPase activity, facilitates female sexual development by maintaining gonadotrophin-releasing hormone neuronal excitability. [electronic resource] by Garcia-Rudaz, C Deng, V Matagne, V Ronnekleiv, O K Bosch, M Han, V Percy, A K Ojeda, S R Producer: 20090428 In: Journal of neuroendocrinology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Glycolipids and glycosyltransferases in permanent cell lines established from human medulloblastomas. [electronic resource] by Gottfries, J Percy, A K Månsson, J E Fredman, P Wikstrand, C J Friedman, H S Bigner, D D Svennerholm, L Producer: 19910408 In: Biochimica et biophysica acta vol. 1081 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	The pattern of growth failure in Rett syndrome. [electronic resource] by Schultz, R J Glaze, D G Motil, K J Armstrong, D D del Junco, D J Hubbard, C R Percy, A K Producer: 19930707 In: American journal of diseases of children (1960) vol. 147 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. [electronic resource] by Ellison, K A Fill, C P Terwilliger, J DeGennaro, L J Martin-Gallardo, A Anvret, M Percy, A K Ott, J Zoghbi, H Producer: 19920304 In: American journal of human genetics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	105.	Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. [electronic resource] by Amir, R E Fang, P Yu, Z Glaze, D G Percy, A K Zoghbi, H Y Roa, B B Van den Veyver, I B Producer: 20060420 In: Journal of medical genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	Population-based registries using multidisciplinary reporters: a method for the study of pediatric neurologic disorders. [electronic resource] by Kozinetz, C A Skender, M L MacNaughton, N L del Junco, D J Almes, M J Schultz, R J Glaze, D G Percy, A K Producer: 19950707 In: Journal of clinical epidemiology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus. [electronic resource] by Kaler, S G Gallo, L K Proud, V K Percy, A K Mark, Y Segal, N A Goldstein, D S Holmes, C S Gahl, W A Producer: 19950309 In: Nature genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	Rett syndrome: controlled study of an oral opiate antagonist, naltrexone. [electronic resource] by Percy, A K Glaze, D G Schultz, R J Zoghbi, H Y Williamson, D Frost, J D Jankovic, J J del Junco, D Skender, M Waring, S Producer: 19940510 In: Annals of neurology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	Determination of gangliosides in six human primary medulloblastomas. [electronic resource] by Gottfries, J Fredman, P Månsson, J E Collins, V P von Holst, H Armstrong, D D Percy, A K Wikstrand, C J Bigner, D D Svennerholm, L Producer: 19901017 In: Journal of neurochemistry vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Clinical and genetic heterogeneity in benign hereditary chorea. [electronic resource] by Breedveld, G J Percy, A K MacDonald, M E de Vries, B B A Yapijakis, C Dure, L S Ippel, E F Sandkuijl, L A Heutink, P Arts, W F M Producer: 20020920 In: Neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Epilepsy and the natural history of Rett syndrome. [electronic resource] by Glaze, D G Percy, A K Skinner, S Motil, K J Neul, J L Barrish, J O Lane, J B Geerts, S P Annese, F Graham, J McNair, L Lee, H-S Producer: 20100409 In: Neurology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Early progressive encephalopathy in boys and MECP2 mutations. [electronic resource] by Kankirawatana, P Leonard, H Ellaway, C Scurlock, J Mansour, A Makris, C M Dure, L S Friez, M Lane, J Kiraly-Borri, C Fabian, V Davis, M Jackson, J Christodoulou, J Kaufmann, W E Ravine, D Percy, A K Producer: 20060808 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. [electronic resource] by Amir, R E Van den Veyver, I B Schultz, R Malicki, D M Tran, C Q Dahle, E J Philippi, A Timar, L Percy, A K Motil, K J Lichtarge, O Smith, E O Glaze, D G Zoghbi, H Y Producer: 20000531 In: Annals of neurology vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	114.	Clinical severity and quality of life in children and adolescents with Rett syndrome. [electronic resource] by Lane, J B Lee, H-S Smith, L W Cheng, P Percy, A K Glaze, D G Neul, J L Motil, K J Barrish, J O Skinner, S A Annese, F McNair, L Graham, J Khwaja, O Barnes, K Krischer, J P Producer: 20120105 In: Neurology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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