18 results for author:"Figlewicz D.A." in Literature citations
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| Lack of association between VEGF gene polymorphisms and plasma VEGF levels and sporadic AL. Golenia A., Tomik B., Zawislak D., Wolkow P., Dziubek A., Sado M., Szczudlik A., Figlewicz D.A., Slowik A. Neurology 75:2035-2037(2010) · Mapped (7) |
| A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. Wills A.M., Cronin S., Slowik A., Kasperaviciute D., Van Es M.A., Morahan J.M., Valdmanis P.N., Meininger V., Melki J., Shaw C.E. et al. Neurology 73:16-24(2009) · Mapped (3) |
| Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALS. Meisler M.H., Russ C., Montgomery K.T., Greenway M., Ennis S., Hardiman O., Figlewicz D.A., Quenneville N.R., Conibear E., Brown R.H. Jr. Amyotroph Lateral Scler 9:141-148(2008) · Mapped (3) |
| Paraoxonase 2 gene C311S polymorphism is associated with a risk of large vessel disease stroke in a Polish population. Slowik A., Wloch D., Szermer P., Wolkow P., Malecki M., Pera J., Turaj W., Dziedzic T., Klimkowicz-Mrowiec A., Kopec G. et al. Cerebrovasc. Dis. 23:395-400(2007) · Mapped (9) |
| Paraoxonase gene polymorphisms and sporadic ALS. Slowik A., Tomik B., Wolkow P.P., Partyka D., Turaj W., Malecki M.T., Pera J., Dziedzic T., Szczudlik A., Figlewicz D.A. Neurology 67:766-770(2006) · Mapped (11) |
| Alpha1-antichymotrypsin gene (SERPINA3) A/T polymorphism as a risk factor for aneurysmal subarachnoid hemorrhage. Slowik A., Borratynska A., Turaj W., Pera J., Dziedzic T., Figlewicz D.A., Betlej M., Krzyszkowski T., Czepko R., Szczudlik A. Stroke 36:737-740(2005) · Mapped (4) |
| Coagulation factor XIII VaI34Leu polymorphism in patients with small vessel disease or primary intracerebral hemorrhage. Slowik A., Dziedzic T., Pera J., Figlewicz D.A., Szczudlik A. Cerebrovasc. Dis. 19:165-170(2005) · Mapped (4) |
| DD genotype of ACE gene is a risk factor for intracerebral hemorrhage. Slowik A., Turaj W., Dziedzic T., Haefele A., Pera J., Malecki M.T., Glodzik-Sobanska L., Szermer P., Figlewicz D.A., Szczudlik A. Neurology 63:359-361(2004) · UniProtKB (1) |
| A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in males. Slowik A., Dziedzic T., Turaj W., Pera J., Glodzik-Sobanska L., Szermer P., Malecki M.T., Figlewicz D.A., Szczudlik A. Stroke 35:1589-1593(2004) · Mapped (5) |
| Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network. Devlin B., Bennett P., Dawson G., Figlewicz D.A., Grigorenko E.L., McMahon W., Minshew N., Pauls D., Smith M., Spence M.A. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 126B:46-50(2004) · Mapped (5) |
| Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia. Meijer I.A., Hand C.K., Cossette P., Figlewicz D.A., Rouleau G.A. Arch. Neurol. 59:281-286(2002) · UniProtKB (1) |
| A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Hadano S., Hand C.K., Osuga H., Yanagisawa Y., Otomo A., Devon R.S., Miyamoto N., Showguchi-Miyata J., Okada Y., Singaraja R. et al. |
| Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders. Ingram J.L., Stodgell C.J., Hyman S.L., Figlewicz D.A., Weitkamp L.R., Rodier P.M. Teratology 62:393-405(2000) · UniProtKB (2) |
| Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Rosen D.R., Siddique T., Patterson D., Figlewicz D.A., Sapp P., Hentati A., Donaldson D., Goto J., O'Regan J.P., Deng H.-X. et al. |
| Polymorphism in the multi-phosphorylation domain of the human neurofilament heavy-subunit-encoding gene. Figlewicz D.A., Rouleau G.A., Krizus A., Julien J.P. Gene 132:297-300(1993) · UniProtKB (1) |
| Mapping of human gamma-glutamyl transpeptidase genes on chromosome 22 and other human autosomes. Figlewicz D.A., Delattre O., Guellaen G., Krizus A., Thomas G., Zucman J., Rouleau G.A. Genomics 17:299-305(1993) · Mapped (15) |
| Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis. Pramatarova A., Figlewicz D.A., Krizus A., Han F.Y., Ceballos-Picot I., Nicole A., Dib M., Meininger V., Brown R.H. Jr., Rouleau G.A. Am. J. Hum. Genet. 56:592-596(1995) · UniProtKB (1) |
| Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis. Figlewicz D.A., Krizus A., Martinoli M.G., Meininger V., Dib M., Rouleau G.A., Julien J.-P. Hum. Mol. Genet. 3:1757-1761(1994) · UniProtKB (1) · Mapped (4) |