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Results: 1-8 |
Results: 8
Parametric linkage analysis and disequilibrium methods to identify loci for complex disease
Authors: McClintick, J Koller, DL Pankratz, N Kirkwood, SC Naughton, B Foroud, T
Citation: J. Mcclintick et al., Parametric linkage analysis and disequilibrium methods to identify loci for complex disease, GENET EPID, 21, 2001, pp. S528-S533
Use of variable marker density, principal components, and neural networks in the dissection of disease etiology
Authors: Pankratz, N Kirkwood, SC Flury, L Koller, DL Foroud, T
Citation: N. Pankratz et al., Use of variable marker density, principal components, and neural networks in the dissection of disease etiology, GENET EPID, 21, 2001, pp. S732-S737
Progression of symptoms in the early and middle stages of Huntington disease
Authors: Kirkwood, SC Su, JL Conneally, PM Foroud, T
Citation: Sc. Kirkwood et al., Progression of symptoms in the early and middle stages of Huntington disease, ARCH NEUROL, 58(2), 2001, pp. 273-278
Relationship of family history scores for stroke and hypertension to quantitative measures of white-matter hyperintensities and stroke volume in elderly males
Authors: Reed, T Kirkwood, SC DeCarli, C Swan, GE Miller, BL Wolf, PA Jack, LM Carmelli, D
Citation: T. Reed et al., Relationship of family history scores for stroke and hypertension to quantitative measures of white-matter hyperintensities and stroke volume in elderly males, NEUROEPIDEM, 19(2), 2000, pp. 76-86
Subtle changes among presymptomatic carriers of the Huntington's disease gene
Authors: Kirkwood, SC Siemers, E Hodes, ME Conneally, PM Christian, JC Foroud, T
Citation: Sc. Kirkwood et al., Subtle changes among presymptomatic carriers of the Huntington's disease gene, J NE NE PSY, 69(6), 2000, pp. 773-779
Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene
Authors: Kirkwood, SC Siemers, E Bond, C Conneally, PM Christian, JC Foroud, T
Citation: Sc. Kirkwood et al., Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene, ARCH NEUROL, 57(7), 2000, pp. 1040-1044
Linkage of Type II and Type III cystinuria to 19q13.1: Codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone-forming phenotype
Authors: Stoller, ML Bruce, JE Bruce, CA Foroud, T Kirkwood, SC Stambrook, PJ
Citation: Ml. Stoller et al., Linkage of Type II and Type III cystinuria to 19q13.1: Codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone-forming phenotype, AM J MED G, 86(2), 1999, pp. 134-139
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers
Authors: Kirkwood, SC Siemers, E Stout, JC Hodes, ME Conneally, PM Christian, JC Foroud, T
Citation: Sc. Kirkwood et al., Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers, ARCH NEUROL, 56(5), 1999, pp. 563-568
Risultati: 1-8 |