Papers authored by Hand CK

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A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.
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Fernandez DM, Hand CK, Sweeney BJ, and Parfrey NA
Headache 48(1):101, 2008 Jan - Who cited this? | PubMed ID: 18184292 | Fulltext
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A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy.
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Grewal KK, Stefanelli MG, Meijer IA, Hand CK, Rouleau GA, and Ives EJ
American journal of medical genetics. Part A 131(3):249-54, 2004 Dec 15 - Who cited this? | PubMed ID: 15523628 | Fulltext
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Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.
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Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, Bouchard JP, Camu W, Hayden MR, and Rouleau GA
Archives of neurology 60(12):1768-71, 2003 Dec - Who cited this? | PubMed ID: 14676054 | Fulltext
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Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families.
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Koenekoop RK, Loyer M, Hand CK, Al Mahdi H, Dembinska O, Beneish R, Racine J, and Rouleau GA
American journal of ophthalmology 136(4):678-87, 2003 Oct - Who cited this? | PubMed ID: 14516808 | Fulltext
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Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.
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Dupré N, Verlaan DJ, Hand CK, Laurent SB, Turecki G, Davenport WJ, Acciarri N, Dichgans J, Ohkuma A, Siegel AM, and Rouleau GA
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 30(2):122-8, 2003 May - Who cited this? | PubMed ID: 12774951 | Fulltext
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An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred.
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Gros-Louis F, Meijer IA, Hand CK, Dubé MP, MacGregor DL, Seni MH, Devon RS, Hayden MR, Andermann F, Andermann E, and Rouleau GA
Annals of neurology 53(1):144-5, 2003 Jan - Who cited this? | PubMed ID: 12509863 | Fulltext
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A locus for autosomal dominant hereditary spastic ataxia, SAX1, maps to chromosome 12p13.
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Meijer IA, Hand CK, Grewal KK, Stefanelli MG, Ives EJ, and Rouleau GA
American journal of human genetics 70(3):763-9, 2002 Mar - Who cited this? | PubMed ID: 11774073 | Fulltext
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Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.
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Meijer IA, Hand CK, Cossette P, Figlewicz DA, and Rouleau GA
Archives of neurology 59(2):281-6, 2002 Feb - Who cited this? | PubMed ID: 11843700 | Fulltext
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Familial amyotrophic lateral sclerosis.
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Hand CK and Rouleau GA
Muscle & nerve 25(2):135-59, 2002 Feb - Who cited this? | PubMed ID: 11870681 | Fulltext
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A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.
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Hand CK, Khoris J, Salachas F, Gros-Louis F, Lopes AA, Mayeux-Portas V, Brewer CG, Brown RH, Meininger V, Camu W, and Rouleau GA
American journal of human genetics 70(1):251-6, 2002 Jan - Who cited this? | PubMed ID: 11706389 | Fulltext
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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
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Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, 
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Nature genetics 29(2):166-73, 2001 Oct - Who cited this? | PubMed ID: 11586298 | Fulltext
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Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.
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Hand CK, Mayeux-Portas V, Khoris J, Briolotti V, Clavelou P, Camu W, and Rouleau GA
Annals of neurology 49(2):267-71, 2001 Feb - Who cited this? | PubMed ID: 11220750 | Fulltext
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A founder mutation in French-Canadian families with X-linked hereditary neuropathy.
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Dupré N, Cossette L, Hand CK, Bouchard JP, Rouleau GA, and Puymirat J
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 28(1):51-5, 2001 Feb - Who cited this? | PubMed ID: 11252295 | Fulltext
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Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
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Hand CK, Harmon DL, Kennedy SM, FitzSimon JS, Collum LM, and Parfrey NA
Genomics 61(1):1-4, 1999 Oct 1 - Who cited this? | PubMed ID: 10512674 | Fulltext
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Homozygosity mapping and linkage analysis demonstrate that autosomal recessive congenital hereditary endothelial dystrophy (CHED) and autosomal dominant CHED are genetically distinct.
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Callaghan M, Hand CK, Kennedy SM, FitzSimon JS, Collum LM, and Parfrey NA
The British journal of ophthalmology 83(1):115, 1999 Jan - Who cited this? | PubMed ID: 10209448 | Fulltext
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