Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Linda Surh"'
Autor:
Sandra L Close, Stuart Hobbs, Lawrence J. Lesko, Michael Pacanowski, Linda Surh, Arlene R Hughes, Susanne B. Haga, Nadine Cohen, Michael Mosteller, Scott Gottlieb, Marisa Papaluca-Amati, Myong-Jin Kim, Scott D. Patterson, Issam Zineh, Bryan Dechairo
Publikováno v:
Pharmacogenomics. 11:1637-1647
The 2010 US FDA–Drug Industry Association (DIA) Pharmacogenomics (PGx) Workshop follows a series that began in 2002 bringing together multidisciplinary experts spanning regulatory authorities, medical research, healthcare and industry. This report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc11c12f1a71f3198efeafc101270f09
https://doi.org/10.2217/pgs.10.138
https://doi.org/10.2217/pgs.10.138
Autor:
Lawrence J. Lesko, Steve Gutman, M. J. Finley Austin, Oscar Della Pasqua, Stuart Hobbs, Lori M. Minasian, Kan Lu, Linda Surh
Publikováno v:
Pharmacogenomics. 10:137-147
Over the past four years, the annual US FDA–DIA pharmacogenomic workshops have brought together attendees with wide-ranging expertise spanning industry, regulatory authorities and academia. This special report summarizes a breakout session using a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c9841391b557bfc0bd06354eb9a3f50
https://doi.org/10.2217/14622416.10.1.137
https://doi.org/10.2217/14622416.10.1.137
Autor:
Judith A Wessels, Evelyne Jacqz-Aigrain, Ineke Jonker, Ron H.N. van Schaik, Chiara Piana, Achille Iolascon, Roberta Russo, Sabine Fürst-Recktenwald, Linda Surh, Oscar Della Pasqua
Publikováno v:
Journal of Clinical Pharmacology, 52(5), 704-716
The Journal of Clinical Pharmacology; Vol 52
The Journal of Clinical Pharmacology
The Journal of Clinical Pharmacology; Vol 52
The Journal of Clinical Pharmacology
This article aims to provide an overview of the current situation regarding pharmacogenetic and pharmacogenomic (PG) studies in pediatrics, with a special focus on the role of PG data in the regulatory decision-making process. Despite the gap in phar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282cc4a1a818f2f04c03daa73bb05f79
https://hdl.handle.net/1887/97800
https://hdl.handle.net/1887/97800
Two 5q13 simple tandem repeat loci are in linkage disequilibrium with Type 1 spinal muscular atrophy
Autor:
Joh-E. lkeda, Alexander E.MacKenzle, Arthur H.M. Burghes, Maysoon Salih, Robert G.Kornelukw, Louise R. Simard, Natalie Roy, Linda Surh, Michael Mclean
Publikováno v:
Human Molecular Genetics. 3:1951-1956
The gene for the common recessive neuromuscular disorder spinal muscular atrophy (SMA) has been previously mapped to chromosome 5q. We report here linkage disequilibrium analyses of two polymorphic simple tandem repeat (STR) sequences which map into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f1de7338ea74c3162992e7f4f4817b
https://doi.org/10.1093/hmg/3.11.1951
https://doi.org/10.1093/hmg/3.11.1951
Autor:
Andrew Kertesz, Luis Fornazzari, Margaret G. Ehm, Simon Lovestone, Paul M. Matthews, Daniella Dhalla, Rachel L. Taylor, John Wherrett, Karen S. King, Hao Li, Danilo Guzman, William Pryse-Phillips, Sandra W. Stinnett, Pamela L. St. Jean, Rab K. Prinjha, Ruchi Upmanyu, Sally Wetten, Jill C. Richardson, David P. Yarnall, Jina E. Swartz, Natalie Coletta, David A. Hosford, Howard Feldman, Allen D. Roses, Linda Surh, Sandra Hammond, Ging-Yuek Robin Hsiung, Julie Williams, Mary Plumpton, Michael Borrie, Ron Keren, Joan Johnson, Li Li, Neil Goodgame, Peter St George-Hyslop, Richard Delisle, Devon D. Kelly, Paul Hollingworth, Michael C. Irizarry, James David Briley, Ann M. Saunders, Inge Loy-English, Michael John Owen, Rachel A. Gibson, Serge Gauthier, Andrew J. Slater, Lefkos T. Middleton, Michael R. Barnes
Publikováno v:
Archives of neurology. 65(1)
Objective To identify single-nucleotide polymorphisms (SNPs) associated with risk and age at onset of Alzheimer disease (AD) in a genomewide association study of 469 438 SNPs. Design Case-control study with replication. Setting Memory referral clinic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68aeede1e9f58c3b187c1137726087fa
https://pubmed.ncbi.nlm.nih.gov/17998437
https://pubmed.ncbi.nlm.nih.gov/17998437
Autor:
Rajesh Pahwa, Ray L. Watts, Nobutaka Hattori, Lefkos T. Middleton, Samia Ben Yahmed, Alan Freeman, David Leppert, Leigh Ragone, N. Gouider-Khouja, Jina E. Swartz, Ramu Elango, Fayçal Hentati, Liling Warren, Joseph Jankovic, Anthony Akkari, M. Kefi, Catherine L. Wielinski, Christine Hunter, Rim Amouri, Ghada El Euch-Fayeche, Martha Nance, Mourad Zouari, Linda Surh, Lianna Ishihara, Kelly E. Lyons, Rachel A. Gibson, Samia Ben Sassi, David J. Burn, Siwan Thomas, Kevin H. Reeves
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 22(1)
Mutations in the leucine-rich repeat kinase-2 gene (LRRK2) are responsible for some forms of familial as well as sporadic Parkinson's disease (PD). The purpose of this study was to examine the frequency of a single pathogenic mutation (6055G>A) in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfe8082fac695c3e260a38dcd863bf77
https://pubmed.ncbi.nlm.nih.gov/17115391
https://pubmed.ncbi.nlm.nih.gov/17115391
Autor:
Nina Apanasiewicz, Robin Hsiung, William Pryse-Phillips, Dielle Miranda, Rachel Newton, Michael Borrie, Ron Keren, Shailesh Nadkarni, Howard Feldman, Peter St George-Hyslop, Luis Fornazzari, John Wherrett, Anthony Guzman, Inge Loy-English, Serge Gauthier, Rachel A. Gibson, Linda Surh, Alexandra Salvarrey, Andrew Kertesz
Publikováno v:
Neurobiology of Aging. 25:S323
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8710e545836b3aa76becbf6c5c7a97d
https://doi.org/10.1016/s0197-4580(04)81062-5
https://doi.org/10.1016/s0197-4580(04)81062-5
Autor:
Inge Loy-English, Luis Fornazzari, Howard Feldman, Peter St George-Hyslop, Richard Delisle, Andrew Kertesz, Serge Gauthier, William Pryse-Phillips, Ron Keren, Rachel A. Gibson, Danilo Guzman, John Wherrett, Michael Borrie, Linda Surh, Zaven Khatchaturian
Publikováno v:
Neurobiology of Aging. 25:S138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e75295b9b9e3b7e8837ec92c80e6d31
https://doi.org/10.1016/s0197-4580(04)80462-7
https://doi.org/10.1016/s0197-4580(04)80462-7
Autor:
Linda Surh, Stanley E. Read
Publikováno v:
The Journal of Pediatrics. 105:585-587
T o x i c SHOCK SYNDROME has recently gained prominence as a mult isystem disorder associated with shock and Staphylococcus aureus in menstruat ing women wearing tampons. However, Todd et al. ~ first described this entity in 1978 in children with an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e81eb4540cfb415591c0afd8da8c9a3
https://doi.org/10.1016/s0022-3476(84)80424-2
https://doi.org/10.1016/s0022-3476(84)80424-2
Publikováno v:
Pediatrics. 68(4)
Dietary deficiency of biotin was documented in an 11-year-old retarded boy as a consequence of a dietary prescription containing raw eggs. Clinical manifestations were alopecia totalis and an erythematous, exfoliative dermatosis. Metabolic characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd18569085544cf62b314d7acbe27f9
https://pubmed.ncbi.nlm.nih.gov/7322688
https://pubmed.ncbi.nlm.nih.gov/7322688