Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study by PERICAK-VANCE, Margaret A, RIMMLER, Jackie B, LYON-CAEN, Olivier, FONTAINE, Bertrand, DUHAMEL, Emmanuelle, COPPIN, Helene, BRASSAT, David, ROTH, Marie-Paule, CLANET, Michel, ALIZADEH, Mehdi, YAOUANQ, Jacqueline, QUELVENNEC, Erwann, HAINES, Jonathan L, SEMANA, Gilbert, EDAN, Gilles, BABRON, Marie-Claude, GENIN, Emmanuelle, CLERGET-DARPOUX, Francoise, GARCIA, Melissa E, OKSENBERG, Jorge R, BARCELLOS, Lisa F, LINCOLN, Robin, HAUSER, Stephen L, COURNU-REBEIX, Isabelle, AZOULAY-CAYLA, Ariele

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Linkage of the MHC to Familial Multiple Sclerosis Suggests Genetic Heterogeneity by Haines, Jonathan L., Terwedow, Henry A., Burgess, Katie, Pericak-Vance, Margaret A., Rimmler, Jackie B., Martin, Eden R., Oksenberg, Jorge R., Lincoln, Robin, Zhang, David Y., Banatao, Diosdado R., Gatto, Nicole, Goodkin, Donald E., Hauser, Stephen L.

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Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis by Siddique, T, Pericak-Vance, M A, Caliendo, J, Hong, S T, Hung, W Y, Kaplan, J, McKenna-Yasek, D, Rimmler, J B, Sapp, P, Saunders, A M, Scott, W K, Siddique, N, Haines, J L, Brown, R H

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Linkage analysis of candidate myelin genes in familial multiple sclerosis by Seboun, E, Oksenberg, J R, Rombos, A, Usuku, K, Goodkin, D E, Lincoln, R R, Wong, M, Pham-Dinh, D, Boesplug-Tanguy, O, Carsique, R, Fitoussi, R, Gartioux, C, Reyes, C, Ribierre, F, Faure, S, Fizames, C, Gyapay, G, Weissenbach, J, Dautigny, A, Rimmler, J B, Garcia, M E, Pericak-Vance, M A, Haines, J L, Hauser, S L

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CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis by Barcellos, L. F., Schito, A. M., Rimmler, J. B., Vittinghoff, E., Shih, A., Lincoln, R., Callier, S., Elkins, M. K., Goodkin, D. E., Haines, J. L., Pericak-Vance, M. A., Hauser, S. L., Oksenberg, J. R.

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ClinicalTrials.gov Reporting: Strategies for Success at an Academic Health Center by O'Reilly, Erin K., Hassell, Nancy J., Snyder, Denise C., Natoli, Susan, Liu, Irwin, Rimmler, Jackie, Amspacher, Valerie, Burnett, Bruce K., Parrish, Amanda B., Berglund, Jelena P., Stacy, Mark

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Linkage of frontotemporal dementia to chromosome 17 : Clinical and neuropathological characterization of phenotype by YAMAOKA, L. H, WELSH-BOHMER, K. A, PERICAK-VANCE, M. A, HULETTE, C. M, GASKELL, P. C, MURRAY, M, RIMMLER, J. L, ROSI HELMS, B, GUERRA, M, ROSES, A. D, SCHMECHEL, D. E

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Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers by Hentati, A, Ouahchi, K, Pericak-Vance, M A, Nijhawan, D, Ahmad, A, Yang, Y, Rimmler, J, Hung, W, Schlotter, B, Ahmed, A, Ben Hamida, M, Hentati, F, Siddique, T

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