Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jackie B. Rimmler"'
Autor:
Erin K. O'Reilly, Amanda B. Parrish, Susan Natoli, Nancy Hassell, Jelena P. Berglund, Irwin M. Liu, Denise C. Snyder, Mark Stacy, Valerie Amspacher, Bruce K. Burnett, Jackie B. Rimmler
Publikováno v:
Clinical and Translational Science. 8:48-51
The Food and Drug Administration Amendments Act of 2007 (FDAAA 2007, US Public Law 110-98) mandated registration and reporting of results for applicable clinical trials (ACTs). Meeting these registration and results reporting requirements has proven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b46333ba107c68af67fc0cdb5f2ed304
https://doi.org/10.1111/cts.12235
https://doi.org/10.1111/cts.12235
Autor:
Mehdi Alizadeh, Lisa F. Barcellos, Françoise Clerget-Darpoux, David Brassat, Marie Claude Babron, M. Clanet, Margaret A. Pericak-Vance, Robin R. Lincoln, Stephen L. Hauser, Isabelle Cournu-Rebeix, Gilbert Semana, Erwann Quelvennec, Emmanuelle Génin, Melissa E. Garcia, Jorge R. Oksenberg, Hélène Coppin, J. Yaouanq, Ariele Azoulay-Cayla, Gilles Edan, Jonathan L. Haines, Olivier Lyon-Caen, M.-P. Roth, Emmanuelle Duhamel, Jackie B. Rimmler, Bertrand Fontaine
Publikováno v:
neurogenetics. 5:45-48
Multiple sclerosis (MS) is a demyelinating autoimmune disease with a strong yet complex genetic component. To date only the HLA-DR locus, and specifically the HLA-DR15 allele, has been identified and confirmed as influencing the risk of developing MS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54f938ae669e4dccc469dccdb31ff478
https://doi.org/10.1007/s10048-003-0163-y
https://doi.org/10.1007/s10048-003-0163-y
Autor:
Jonathan L. Haines, Donald E. Goodkin, Robin R. Lincoln, Stephen L. Hauser, Jorge R. Oksenberg, Jackie B. Rimmler, Stacy Callier, Eric Vittinghoff, Andrew Shih, Margaret A. Pericak-Vance, Lisa F. Barcellos, Anna M. Schito, Mary K. Elkins
Publikováno v:
Immunogenetics. 51:281-288
Multiple sclerosis (MS) is a common disease of the central nervous system characterized by myelin loss and progressive neurological dysfunction. An underlying genetic susceptibility plays a clear role in the etiology of MS, likely acting in concert w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::540b84b48bb8db440c4f6d370bda9cc4
https://doi.org/10.1007/s002510050621
https://doi.org/10.1007/s002510050621
Autor:
Jonathan L. Haines, Jackie B. Rimmler, O. Boesplug-Tanguy, Margaret A. Pericak-Vance, A. Dautigny, Melissa E. Garcia, Sabine Fauré, C. Gartioux, Cécile Fizames, Florence Ribierre, Robin R. Lincoln, R. Carsique, Stephen L. Hauser, Antony Rombos, Jorge R. Oksenberg, Eric Seboun, R. Fitoussi, Cecile Reyes, D. Pham-Dinh, Koishiro Usuku, Gabor Gyapay, Donald E. Goodkin, Jean Weissenbach, Michael Wong
Publikováno v:
neurogenetics. 2:155-162
Multiple sclerosis (MS) is an autoimmune demyelinating disease of the central nervous system. A complex genetic etiology is thought to underlie susceptibility to this disease. The present study was designed to analyze whether differences in genes tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbd1aade10c3431b8b571eed7a008e11
https://doi.org/10.1007/s100480050076
https://doi.org/10.1007/s100480050076
Autor:
Christiane Ben Hamida, Jackie B. Rimmler, Wu Yen Hung, Marcy C. Speer, Afif Hentati, Margaret A. Pericak-Vance, Jonathan L. Haines, Robert H. Brown, Khemissa Bejaoui, Denise A. Figlewicz, Fayçal Hentati, Mongi Ben Hamida, Teepu Siddique
Publikováno v:
Nature Genetics. 7:425-428
Amyotrophic lateral sclerosis (ALS) usually presents as a sporadic disorder of motor neurons. However, familial forms of ALS have been described--autosomal dominant forms (ALS1, ALS3), clinically indistinguishable from the sporadic form, and autosoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed1c90dcff42eeb75986892336b2180c
https://doi.org/10.1038/ng0794-425
https://doi.org/10.1038/ng0794-425
Autor:
Jackie B. Rimmler, Diane McKenna-Yasek, Robert H. Brown, Peter C. Sapp, Margaret A. Pericak-Vance, William K. Scott, Janice Caliendo, Seong-Tshool Hong, Jonathan L. Haines, Jocelyn Kaplan, Ann M. Saunders, Nailah Siddique, Teepu Siddique, Wu Yen Hung
Publikováno v:
Neurogenetics. 1(3)
Amyotrophic lateral sclerosis (ALS) is a neuro-degenerative disorder with both sporadic and familial forms. Approximately 20% of autosomal dominant ALS is caused by mutations in the Cu/Zn superoxide dismutase (SOD1) gene. The causes of the remaining
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bb29d44b6352ea0672556f70dc8dd69
https://pubmed.ncbi.nlm.nih.gov/10737125
https://pubmed.ncbi.nlm.nih.gov/10737125
Autor:
Wu Yen Hung, Beate Schlotter, Margaret A. Pericak-Vance, Karim Ouahchi, Mongi Ben Hamida, Jackie B. Rimmler, Arsalan Ahmad, Teepu Siddique, Afif Hentati, Yi Yang, Akhtar Ahmed, Fayçal Hentati, Deepak Nijhawan
Publikováno v:
Neurogenetics. 2(1)
Autosomal recessive familial amyotrophic lateral sclerosis (RFALS) is a rare form of ALS that usually presents at an early age with slow progression of symptoms. RFALS is clinically and genetically heterogeneous and the locus of RFALS type 3 was mapp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c4eacc9df7e856f1a19e7776d348484
https://pubmed.ncbi.nlm.nih.gov/9933301
https://pubmed.ncbi.nlm.nih.gov/9933301
Autor:
Diosdado R. Banatao, Jackie B. Rimmler, Margaret A. Pericak-Vance, Nicole M. Gatto, Donald E. Goodkin, Eden R. Martin, Jorge R. Oksenberg, Jonathan L. Haines, David Y. Zhang, Robin R. Lincoln, Stephen L. Hauser, Katie Burgess, Henry Terwedow
Publikováno v:
Human molecular genetics. 7(8)
Multiple sclerosis (MS) is a demyelinating autoimmune disease of the central nervous system. While its etiology is not well understood, genetic factors are clearly involved. Until recently, most genetic studies in MS have been association studies usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb322b62ee0b737f916457cb2aa54779
https://pubmed.ncbi.nlm.nih.gov/9668163
https://pubmed.ncbi.nlm.nih.gov/9668163
Autor:
J. L. Haines, Teepu Siddique, Jackie B. Rimmler, Benjamin Rix Brooks, Nailah Siddique, Robert H. Brown, Seong-Tshool Hong, M. A. Pericak Vance, W. Y. Hung, Jocelyn Kaplan
Publikováno v:
Neurology. 51:310-310
“Late Breaking News” (formerly “Works in Progress”) is a feature of the Scientific Program of the American Academy of Neurology Annual Meeting. It focuses on current ongoing neuroscience research. Late Breaking News posters are selected on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::816339428b1e3c13690ffd4bb0c7c6ec
https://doi.org/10.1212/wnl.51.1.310
https://doi.org/10.1212/wnl.51.1.310