Search Results - "Plaetke, R"

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  1. 1

    Drooling is no early sign of dysphagia in Parkinson's disease by Nienstedt, J C, Buhmann, C, Bihler, M, Niessen, A, Plaetke, R, Gerloff, C, Pflug, C

    Published in Neurogastroenterology and motility (01-04-2018)
    “…Dysphagia is frequent and clinically highly relevant in Parkinson's disease (PD). For a rational dysphagia screening predictors are required. Previous…”
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  2. 2

    Drooling is no early sign of dysphagia in Parkinson′s disease by Nienstedt, J. C., Buhmann, C., Bihler, M., Niessen, A., Plaetke, R., Gerloff, C., Pflug, C.

    Published in Neurogastroenterology and motility (01-04-2018)
    “…Background Dysphagia is frequent and clinically highly relevant in Parkinson's disease (PD). For a rational dysphagia screening predictors are required…”
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    Journal Article
  3. 3

    Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome : Evidence for myelin basic protein haploinsufficiency by GAY, C. T, HARDIES, L. J, SCHIFF, J. M, KAYE, C. I, LEACH, R. J, FOX, P. T, RAUCH, R. A, LANCASTER, J. L, PLAETKE, R, DUPONT, B. R, CODY, J. D, CORNELL, J. E, HERNDON, R. C, GHIDONI, P. D

    Published in American journal of medical genetics (25-07-1997)
    “…Magnetic resonance imaging (MRI) and MRI relaxometry were used to investigate disturbed brain myelination in 18q- syndrome, a disorder characterized by mental…”
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  4. 4

    Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees by COON, H, BYERLEY, W, PLAETKE, R, HOLIK, J, HOFF, M, MYLES-WORSLEY, M, LANNFELT, L, SOKOLOFF, P, SCHWARTZ, J.-C, WALDO, M, FREEDMAN, R

    Published in American journal of human genetics (01-02-1993)
    “…Alterations in dopamine neurotransmission have been strongly implicated in the pathogenesis of schizophrenia for nearly 2 decades. Recently, the genes for five…”
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  5. 5

    A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance by COON, H, JENSEN, S, HOFF, M, HOLIK, J, PAETKE, R, REIMHERR, F, WENDER, P, LEPPERT, M, BYERLEY, W

    Published in American journal of human genetics (01-06-1993)
    “…Manic-depressive illness (MDI), also known as "bipolar affective disorder," is a common and devastating neuropsychiatric illness. Although pivotal biochemical…”
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  6. 6

    Characterization of eight VNTR loci by agarose gel electrophoresis by Odelberg, S J, Plaetke, R, Eldridge, J R, Ballard, L, O'Connell, P, Nakamura, Y, Leppert, M, Lalouel, J M, White, R

    Published in Genomics (San Diego, Calif.) (01-11-1989)
    “…Allelic frequencies and their confidence intervals were obtained for eight independent VNTR loci from a sample of more than 75 Utah Caucasians. Using…”
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    Risk perceptions among patients and their relatives regarding prostate cancer and its heredity by Arar, N, Thompson, I, Sarosdy, M, Harris, M, Shepherd, D, Troyer, D, Plaetke, R

    Published in Prostate cancer and prostatic diseases (01-11-2000)
    “…We performed a qualitative study to examine how prostate cancer (PC) patients and their spouses and relatives take into account family history when considering…”
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    Genetic mapping of the BRCA1 region on chromosome 17q21 by Albertsen, H, Plaetke, R, Ballard, L, Fujimoto, E, Connolly, J, Lawrence, E, Rodriguez, P, Robertson, M, Bradley, P, Milner, B

    Published in American journal of human genetics (01-03-1994)
    “…Chromosome 17q21 harbors a gene (BRCA1) associated with a hereditary form of breast cancer. As a step toward identification of this gene itself we developed a…”
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  9. 9

    Reassignment of the 92-kDa type IV collagenase gene (CLG4B) to human chromosome 20 by Linn, R, DuPont, B R, Knight, C B, Plaetke, R, Leach, R J

    Published in Cytogenetics and cell genetics (01-01-1996)
    “…The collagenase type IV B gene (CLG4B) was previously mapped to human chromosome 16 by hybridization of a cDNA probe to DNAs from a somatic cell hybrid panel…”
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  10. 10

    An extended genetic linkage map and an "index" map for human chromosome 17 by O'Connell, P, Plaetke, R, Matsunami, N, Odelberg, S, Jorde, L, Chance, P, Leppert, M, Lalouel, J M, White, R

    Published in Genomics (San Diego, Calif.) (01-01-1993)
    “…Our previous genetic map for chromosome 17 has been expanded to include 72 loci defined by 90 RFLP markers and four microsatellite markers assayed by the…”
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  11. 11

    Tyrosine hydroxylase gene not linked to manic-depression in seven of eight pedigrees by Byerley, W, Plaetke, R, Hoff, M, Jensen, S, Holik, J, Reimherr, F, Mellon, C, Wender, P, O'Connell, P, Leppert, M

    Published in Human heredity (1992)
    “…We ascertained 8 multigenerational pedigrees afflicted with multiple cases of bipolar and recurrent major depressive disorder. Alterations in dopaminergic and…”
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  12. 12

    The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89 by Hoehe, M R, Ehrenreich, H, Otterud, B, Caenazzo, L, Plaetke, R, Zander, H, Leppert, M

    Published in Cytogenetics and cell genetics (01-01-1993)
    “…We determined the precise genetic location of the human endothelin-1 gene (EDN1), which encodes a peptide with extremely potent vasoactive properties and is…”
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  13. 13

    Linkage analysis of the D1 dopamine receptor gene and manic depression in six families by Jensen, S, Plaetke, R, Holik, J, Hoff, M, O'Connell, P, Reimherr, F, Wender, P, Zhou, Q Y, Civelli, O, Litt, M

    Published in Human heredity (1992)
    “…Disturbances in dopaminergic activity may play an important role in the pathogenesis of manic depression. The effects of dopamine are mediated by at least five…”
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  14. 14

    A genetic linkage map with 29 loci spanning human chromosome 13q by Gerken, S, Leppert, M, O'Connell, P, Cavenee, W, James, C D, Ballard, L, Stauffer, D, Elsner, T, Plaetke, R, Lalouel, J M

    Published in Genomics (San Diego, Calif.) (01-05-1993)
    “…A genetic linkage map for the long arm of human chromosome 13 contains 29 loci derived from 38 probe and enzyme combinations and two protein polymorphisms…”
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    The Family Investigation of Nephropathy and Diabetes (FIND): Design and methods by Knowler, William C., Coresh, Josef, Elston, Robert C., Freedman, Barry I., Iyengar, Sudha K., Kimmel, Paul L., Olson, Jane M., Plaetke, Rosemarie, Sedor, John R., Seldin, Michael F.

    “…The Family Investigation of Nephropathy and Diabetes (FIND) is a multicenter study designed to identify genetic determinants of diabetic nephropathy. It is…”
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    HLA-antigens in a Tunisian familial chondrocalcinosis by Hamza, M, Ayed, K, Bardi, R, Gebuhrer, L, Betuel, H, Bardin, T, Plaetke, R, Lathrop, M

    Published in Disease markers (01-05-1990)
    “…Thirty members of a Tunisian family with hereditary chondrocalcinosis were typed for HLA-A, B, and DR antigens: 7 affected and 23 unaffected subjects in three…”
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    Do Middle School Students Really Have Fixed Images of Elders? by Lichtenstein, Michael J., Pruski, Linda A., Marshall, Carolyn E., Blalock, Cheryl L., Liu, Yan, Plaetke, Rosemarie

    “…Objectives. The purpose of this study was to determine whether combinations of characteristics, abstracted from drawings of elders made by middle school…”
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