Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology
Miller, R G, Jackson, C E, Kasarskis, E J, England, J D, Forshew, D, Johnston, W, Kalra, S, Katz, J S, Mitsumoto, H, Rosenfeld, J, Shoesmith, C, Strong, M J, Woolley, S C
Published in Neurology (13.10.2009)
Published in Neurology (13.10.2009)
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Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology
Miller, R G, Jackson, C E, Kasarskis, E J, England, J D, Forshew, D, Johnston, W, Kalra, S, Katz, J S, Mitsumoto, H, Rosenfeld, J, Shoesmith, C, Strong, M J, Woolley, S C
Published in Neurology (13.10.2009)
Published in Neurology (13.10.2009)
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Longitudinal associations between post-traumatic stress disorder and metabolic syndrome severity
Wolf, E. J., Bovin, M. J., Green, J. D., Mitchell, K. S., Stoop, T. B., Barretto, K. M., Jackson, C. E., Lee, L. O., Fang, S. C., Trachtenberg, F., Rosen, R. C., Keane, T. M., Marx, B. P.
Published in Psychological medicine (01.07.2016)
Published in Psychological medicine (01.07.2016)
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Inclusion body myositis functional rating scale: A reliable and valid measure of disease severity
Jackson, C.E., Barohn, R.J., Gronseth, G., Pandya, S., Herbelin, L.
Published in Muscle & nerve (01.04.2008)
Published in Muscle & nerve (01.04.2008)
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Uterine tumours are a phenotypic manifestation of the hyperparathyroidism‐jaw tumour syndrome
BRADLEY, K. J., HOBBS, M. R., BULEY, I. D., CARPTEN, J. D., CAVACO, B. M., FARES, J. E., LAIDLER, P., MANEK, S., ROBBINS, C. M., SALTI, I. S., THOMPSON, N. W., JACKSON, C. E., THAKKER, R. V.
Published in Journal of internal medicine (01.01.2005)
Published in Journal of internal medicine (01.01.2005)
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Conference Proceeding
Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria
Brooks-Wilson, A R, Kaurah, P, Suriano, G, Leach, S, Senz, J, Grehan, N, Butterfield, Y S N, Jeyes, J, Schinas, J, Bacani, J, Kelsey, M, Ferreira, P, MacGillivray, B, MacLeod, P, Micek, M, Ford, J, Foulkes, W, Australie, K, Greenberg, C, LaPointe, M, Gilpin, C, Nikkel, S, Gilchrist, D, Hughes, R, Jackson, C E, Monaghan, K G, Oliveira, M J, Seruca, R, Gallinger, S, Caldas, C, Huntsman, D
Published in Journal of medical genetics (01.07.2004)
Published in Journal of medical genetics (01.07.2004)
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A preliminary evaluation of a prospective study of pulmonary function studies and symptoms of hypoventilation in ALS/MND patients
Jackson, C.E, Rosenfeld, J, Moore, D.H, Bryan, W.W, Barohn, R.J, Wrench, M, Myers, D, Heberlin, L, King, R, Smith, J, Gelinas, D, Miller, R.G
Published in Journal of the neurological sciences (15.10.2001)
Published in Journal of the neurological sciences (15.10.2001)
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Conference Proceeding
Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene is Associated with Multiple Endocrine Neoplasia Type 2B
Carlson, Katrin M., Dou, Shenshen, Chi, David, Scavarda, Nancy, Toshima, Koji, Jackson, Charles E., Wells, Samuel A., Goodfellow, Paul J., Donis-Keller, Helen
Published in Proceedings of the National Academy of Sciences - PNAS (15.02.1994)
Published in Proceedings of the National Academy of Sciences - PNAS (15.02.1994)
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Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
McAllister, K.A, Oostra, B.A, Porteous, M.E, Jackson, C.E, Heutink, P, Markel, D.S, Letarte, M, McCormick, M.K, Westerman, C.J.J, Guttmacher, A.E, Grogg, K.M, Marchuk, D.A, Johnson, D.W, Baldwin, M.A, Gallione, C.J, Pericak-Vance, M.A, Haitjema, T, Helmbold, E.A, Murrel, J, McKinnon, W.C
Published in Nature genetics (01.12.1994)
Published in Nature genetics (01.12.1994)
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Electrophysiologic findings in multifocal motor neuropathy
Katz, J S, Wolfe, G I, Bryan, W W, Jackson, C E, Amato, A A, Barohn, R J
Published in Neurology (01.03.1997)
Published in Neurology (01.03.1997)
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Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy
Mendell, J R, Barohn, R J, Freimer, M L, Kissel, J T, King, W, Nagaraja, H N, Rice, R, Campbell, W W, Donofrio, P D, Jackson, C E, Lewis, R A, Shy, M, Simpson, D M, Parry, G J, Rivner, M H, Thornton, C A, Bromberg, M B, Tandan, R, Harati, Y, Giuliani, M J
Published in Neurology (27.02.2001)
Published in Neurology (27.02.2001)
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Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas
GOGGINS, M, SCHUTTE, M, KERN, S. E, LU, J, MOSKALUK, C. A, WEINSTEIN, C. L, PETERSEN, G. M, YEO, C. J, JACKSON, C. E, LYNCH, H. T, HRUBAN, R. H
Published in Cancer research (Chicago, Ill.) (01.12.1996)
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Published in Cancer research (Chicago, Ill.) (01.12.1996)
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Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
Johnson, D.W, Berg, J.N, Baldwin, M.A, Gallione, C.J, Marondel, I, Yoon, S.-J, Stenzel, T.T, Speer, M, Pericak-Vance, M.A, Diamond, A, Guttmacher, A.E, Jackson, C.E, Attisano, L, Kucherlapati, R, Porteous, M.E.M, Marchuk, D.A
Published in Nature genetics (01.06.1996)
Published in Nature genetics (01.06.1996)
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Identification of germ-line E-cadherin mutations in gastric cancer families of European origin
GAYTHER, S. A, GORRINGE, K. L, MACLEOD, P, POWELL, S. M, JACKSON, C. E, PONDER, B. A. J, CALDAS, C, RAMUS, S. J, HUNTSMAN, D, ROVIELLO, F, GREHAN, N, MACHADO, J. C, PINTO, E, SERUCA, R, HALLING, K
Published in Cancer research (Chicago, Ill.) (15.09.1998)
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Published in Cancer research (Chicago, Ill.) (15.09.1998)
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Multifocal acquired demyelinating sensory and motor neuropathy: The Lewis-Sumner syndrome
Saperstein, David S., Amato, Anthony A., Wolfe, Gil I., Katz, Jonathan S., Nations, Sharon P., Jackson, Carlayne E., Bryan, Wilson W., Burns, Dennis K., Barohn, Richard J.
Published in Muscle & nerve (01.05.1999)
Published in Muscle & nerve (01.05.1999)
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Maternal lineages and Alzheimer disease risk in the Old Order Amish
VAN DER WALT, Joelle M, SCOTT, William K, KRONER, Charles C, JACKSON, C. E, HAINES, Jonathan L, PERICAK-VANCE, Margaret A, SLIFER, Susan, GASKELL, P. C, MARTIN, Eden R, WELSH-BOHMER, Kathleen, CREASON, Marilyn, CRUNK, Amy, FUZZELL, Denise, MCFARLAND, Lynne
Published in Human genetics (01.11.2005)
Published in Human genetics (01.11.2005)
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Autoimmune Lymphoproliferative Syndrome with Defective Fas: Genotype Influences Penetrance
Jackson, Christine E., Fischer, Roxanne E., Hsu, Amy P., Anderson, Stacie M., Choi, Youngnim, Wang, Jin, Dale, Janet K., Fleisher, Thomas A., Middelton, Lindsay A., Sneller, Michael C., Lenardo, Michael J., Straus, Stephen E., Puck, Jennifer M.
Published in American journal of human genetics (01.04.1999)
Published in American journal of human genetics (01.04.1999)
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Prophylactic total gastrectomy for familial gastric cancer
Lewis, F.R., Mellinger, J.D., Hayashi, A., Lorelli, D., Monaghan, K.G., Carneiro, F., Huntsman, D.G., Jackson, C.E., Caldas, C.
Published in Surgery (01.10.2001)
Published in Surgery (01.10.2001)
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An autosomal genomic screen for dementia in an extended Amish family
Ashley-Koch, A.E., Shao, Y., Rimmler, J.B., Gaskell, P.C., Welsh-Bohmer, K.A., Jackson, C.E., Scott, W.K., Haines, J.L., Pericak-Vance, M.A.
Published in Neuroscience letters (13.05.2005)
Published in Neuroscience letters (13.05.2005)
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