Search Results - "Schlumpf, K"

The strategies to reduce iron deficiency in blood donors randomized trial: design, enrolment and early retention by Bialkowski, W., Bryant, B. J., Schlumpf, K. S., Wright, D. J., Birch, R., Kiss, J. E., D'Andrea, P., Cable, R. G., Spencer, B. R., Vij, V., Mast, A. E.

“…Background and Objectives Repeated blood donation produces iron deficiency. Changes in dietary iron intake do not prevent donation‐induced iron deficiency…”
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A Case-based Reasoning (CBR) model for integrating insurance policy and regulations in a United States physical therapist educational program by Cohn, R, Harwood, K, Richards, H, Schlumpf, K

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Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14 by Mortilla, M, Farrer, L, Liang, Y, Duara, R, St George-Hyslop, P, Sorbi, S, Vaula, G, Rogaev, E, Cantu, J-M, Bergamini, L, Macciardi, F, Rogaeva, E, Pericak-Vance, M, Schlumpf, K, Tsuda, T, Haines, J, Tanzi, R, Nee, L, Rainero, I, Alexandrova, N, Kennedy, J, Pollen, D, Amaducci, L, Polinsky, R, Bruni, A, Roses, A, Lukiw, W, Crapper McLachlan, D, Pinessi, L, Foncin, J-F, Montesi, M, Gusella, J

“…Familial Alzheimer's disease (FAD) has been shown to be genetically heterogeneous, with a very small proportion of early onset pedigrees being associated with…”
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Machado-Joseph disease in pedigrees of Azorean descent is linked to chromosome 14 by ST GEORGE-HYSLOP, P, ROGAEVA, E, KENNEDY, J, WEISSENBACH, J, BILLINGSLEY, G. D, COX, D. W, LANG, A. E, WHERRETT, J. R, HUTERER, J, TSUDA, T, SANTOS, J, HAINES, J. L, SCHLUMPF, K, ROGAEV, E. I, LIANG, Y, MCLACHLAN, D. R. C

“…A locus for Machado-Joseph disease (MJD) has recently been mapped to a 30-cM region of chromosome 14q in five pedigrees of Japanese descent. MJD is a…”
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Hepcidin level predicts hemoglobin concentration in individuals undergoing repeated phlebotomy by Mast, Alan E, Schlumpf, Karen S, Wright, David J, Johnson, Bryce, Glynn, Simone A, Busch, Michael P, Olbina, Gordana, Westerman, Mark, Nemeth, Elizabeta, Ganz, Tomas

“…Dietary iron absorption is regulated by hepcidin, an iron regulatory protein produced by the liver. Hepcidin production is regulated by iron stores,…”
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Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p 12.1 by Lerner, T J, Boustany, R M, MacCormack, K, Gleitsman, J, Schlumpf, K, Breakefield, X O, Gusella, J F, Haines, J L

“…The neuronal ceroid lipofuscinoses (NCL; Batten disease) are a collection of autosomal recessive disorders characterized by the accumulation of autofluorescent…”
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Isolation of a novel gene underlying batten disease, CLN3 by Lerner, Terry J, Boustany, Rose-Mary N, Anderson, John W, D'Arigo, Kenneth L, Schlumpf, Karen, Buckler, Alan J, Gusella, James F, Haines, Jonathan L

“…Batten disease (also known as juvenile neuronal ceroid lipofuscinosis) is a recessively inherited neurodegenerative disorder of childhood characterized by…”
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Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers by Rosen, D R, Sapp, P, O'Regan, J, McKenna-Yasek, D, Schlumpf, K S, Haines, J L, Gusella, J F, Horvitz, H R, Brown, Jr, R H

“…Amyotrophic lateral sclerosis (ALS: Lou Gehrig's Disease) is a lethal neurodegenerative disease of upper and lower motorneurons in the brain and spinal cord…”
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IRTGRAPH: Item Response Theory Graphics Using SAS/GRAPH by Childs, R.A., Schlumpf, K.

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Convenience, the bane of our existence, and other barriers to donating by Schreiber, George B., Schlumpf, Karen S., Glynn, Simone A., Wright, David J., Tu, Yongling, King, Melissa R., Higgins, Martha J., Kessler, Debra, Gilcher, Ronald, Nass, Catharie C., Guiltinan, Anne M.

“…BACKGROUND:  To prevent donor loss and improve retention, it is important to understand the major deterrents to blood donation and to identify factors that can…”
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Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic deposits by Mitchison, H M, O'Rawe, A M, Lerner, T J, Taschner, P E, Schlumpf, K, D'Arigo, K, de Vos, N, Gormally, E, Phillips, H A, Thompson, A D

“…Haplotype analysis in a collaborative collection of 143 families with juvenile-onset neuronal ceroid lipofuscinosis (JNCL) or Batten (Spielmeyer-Vogt-Sjögren)…”
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Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p12.1 by LERNER, T. J, BOUSTANY, R.-M. N, MACCORMACK, K, GLEITSMAN, J, SCHLUMPF, K, BREAKEFIELD, X. O, GUSELLA, J. F, HAINES, J. L

“…The neuronal ceroid lipofuscinoses (NCL; Batten disease) are a collection of autosomal recessive disorders characterized by the accumulation of autofluorescent…”
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Linkage disequilibrium between the juvenile neuronal ceroid lipofuscinosis gene and marker loci on chromosome 16p12. 1 by Lerner, T.J., MacCormack, K., Gleitsman, J., Schlumpf, K., Breakefield, X.O., Gusella, J.F., Haines, J.L.

“…The neuronal ceroid lipofuscinoses (NCL; Batten disease) are a collection of autosomal recessive disorders characterized by the accumulation of autofluorescent…”
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Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic association by Mitchison, H M, Taschner, P E, O'Rawe, A M, de Vos, N, Phillips, H A, Thompson, A D, Kozman, H M, Haines, J L, Schlumpf, K, D'Arigo, K

“…CLN3, the gene for juvenile-onset neuronal ceroid lipofuscinosis (JNCL) or Batten disease, has been localized by genetic linkage analysis to chromosome 16p…”
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Mental health service use in a community head start population by New, Michelle, Razzino, Brian, Lewin, Amy, Schlumpf, Karen, Joseph, Jill

“…Evaluating access to and delivery of mental health services for young children was a primary objective of the national research demonstration program Starting…”
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