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	1.	Familial amyotrophic lateral sclerosis. [electronic resource] by Hand, Collette K Rouleau, Guy A Producer: 20020313 In: Muscle & nerve vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Homozygous SLC4A11 mutation in a large Irish CHED2 pedigree. [electronic resource] by Hand, Collette K McGuire, Mairide Parfrey, Nollaig A Murphy, Conor C Producer: 20171113 In: Ophthalmic genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Chorea-Acanthocytosis and the Huntington Disease Allele in an Irish Family. [electronic resource] by Murphy, Olwen C O'Toole, Orna Hand, Collette K Ryan, Aisling M Producer: 20190319 In: Tremor and other hyperkinetic movements (New York, N.Y.) vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred. [electronic resource] by Fernandez, Desiree M Hand, Collette K Sweeney, Brian J Parfrey, Nollaig A Producer: 20080502 In: Headache vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mutagenesis by Microbe: the Role of the Microbiota in Shaping the Cancer Genome. [electronic resource] by Barrett, Maurice Hand, Collette K Shanahan, Fergus Murphy, Thomas O'Toole, Paul W Producer: 20210611 In: Trends in cancer vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree. [electronic resource] by Skehan, Evelyn B Abdulrahim, Manal M A Parfrey, Nollaig A Hand, Collette K Producer: 20120830 In: Neurogenetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia. [electronic resource] by Meijer, Inge A Hand, Collette K Cossette, P Figlewicz, Denise A Rouleau, Guy A Producer: 20020228 In: Archives of neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Andersen-Tawil syndrome with early fixed myopathy. [electronic resource] by Lefter, Stela Hardiman, Orla Costigan, Donal Lynch, Bryan McConville, John Hand, Collette K Ryan, Aisling M Producer: 20151104 In: Journal of clinical neuromuscular disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Phenotypic Variation in a Caucasian Kindred with Chorea-Acanthocytosis. [electronic resource] by Merwick, Áine Mok, Tzehow McNamara, Brian Parfrey, Nollaig A Moore, Helena Sweeney, Brian J Hand, Collette K Ryan, Aisling M Publication details: Movement disorders clinical practice Mar 2015 In: Movement disorders clinical practice vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families. [electronic resource] by Koenekoop, Robert K Loyer, Magali Hand, Collette K Al Mahdi, Huda Dembinska, Olga Beneish, Raquel Racine, Julie Rouleau, Guy A Producer: 20031009 In: American journal of ophthalmology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis. [electronic resource] by Hand, Collette K Devon, Rebecca S Gros-Louis, Francois Rochefort, Daniel Khoris, Jawad Meininger, Vincent Bouchard, Jean-Pierre Camu, William Hayden, Michael R Rouleau, Guy A Producer: 20040107 In: Archives of neurology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation. [electronic resource] by Dupré, Nicolas Verlaan, Dominique J Hand, Collette K Laurent, Sandra B Turecki, Gustavo Davenport, W Jeptha Acciarri, Nicola Dichgans, Johannes Ohkuma, Akio Siegel, Adrian M Rouleau, Guy A Producer: 20030801 In: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q. [electronic resource] by Hand, Collette K Khoris, Jawad Salachas, François Gros-Louis, François Lopes, Ana Amélia Simões Mayeux-Portas, Veronique Brewer, Carl G Brown, Robert H Meininger, Vincent Camu, William Rouleau, Guy A Producer: 20020125 In: American journal of human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred. [electronic resource] by Gros-Louis, François Meijer, Inge A Hand, Collette K Dubé, Marie-Pierre MacGregor, Daune L Seni, Marie-Hélène Devon, Rebecca S Hayden, Michael R Andermann, Frederick Andermann, Eva Rouleau, Guy A Producer: 20040116 In: Annals of neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)