Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Stephanie L. Burgess"'
Autor:
Stephanie L. Burgess, Yi-Meng Yen, Mininder S. Kocher, Omar F Rahman, Zaamin B Hussain, Mahad M Hassan
Publikováno v:
Orthopaedic Journal of Sports Medicine
Background: Previous studies have examined factors related to the increased use of opioids after hip arthroscopy in adults. However, few have focused on the adolescent population. Purpose: The purpose of this study was to compare the opioids prescrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be74a909193c69fc22d7fbcae06ef7eb
https://doi.org/10.1177/2325967121s00055
https://doi.org/10.1177/2325967121s00055
Autor:
Waleed M. Al-Maneea, Mustafa A. Salih, Louis M. Kunkel, Anna R. Duncan, M.Z. Seidahmed, Hisham Alkhalidi, Salem H. Alshemmari, Stephanie L. Burgess, Abdullah S. Al-Jarallah, Steven E. Boyden, Richard R. Bennett, Elicia Estrella, Peter B. Kang, Alexander J. White
Publikováno v:
Neurogenetics
Limb girdle muscular dystrophy type 2 (LGMD2) is a genetically heterogeneous autosomal recessive disorder caused by mutations in 15 known genes. DNA sequencing of all candidate genes can be expensive and laborious, whereas a selective sequencing appr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f15137f2fe10414451ff7375d4b4cfa
https://doi.org/10.1007/s10048-010-0250-9
https://doi.org/10.1007/s10048-010-0250-9
Autor:
Leah Mallory, Tyler M. Burpee, Stephanie L. Burgess, Louis M. Kunkel, James G. Shaw, Peter B. Kang, Basil T. Darras, Michael S. D. Agus, Elicia Estrella, Samuel Nurko
Publikováno v:
Pediatric neurology. 41(1)
Congenital myasthenic syndrome is difficult to diagnose, especially in the neonate when classic myasthenic signs may not be present. Congenital myasthenic syndrome with episodic apnea is a rare cause of recurrent apnea in infancy. We present an infan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::061e86570747b5fc26321c2b22f22de6
https://pubmed.ncbi.nlm.nih.gov/19520274
https://pubmed.ncbi.nlm.nih.gov/19520274
Autor:
M.Z. Seidahmed, Alexander J. White, Steven E. Boyden, Stephanie L. Burgess, Elicia Estrella, Mustafa A. Salih, Anna R. Duncan, Louis M. Kunkel, Richard R. Bennett, Peter B. Kang
Publikováno v:
Neuromuscular Disorders. 20:604-605
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a55be5bef6e46507c2abbc4b0bb87e4
https://doi.org/10.1016/j.nmd.2010.07.031
https://doi.org/10.1016/j.nmd.2010.07.031
Autor:
Yiping Shen, Alan H. Beggs, Elicia Estrella, Andrew S Cheng, Bai-Lin Wu, Louis M. Kunkel, Va Lip, Caitlin Barrett, Poh San Lai, Hal E. Schneider, Stephanie L. Burgess, Richard R. Bennett, Basil T. Darras
Publikováno v:
BMC Genetics
BMC Genetics, Vol 10, Iss 1, p 66 (2009)
BMC Genetics, Vol 10, Iss 1, p 66 (2009)
Background One of the most common and efficient methods for detecting mutations in genes is PCR amplification followed by direct sequencing. Until recently, the process of designing PCR assays has been to focus on individual assay parameters rather t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56bd6f59461e02b8ba77f3028346a2d7
http://europepmc.org/articles/PMC2781300
http://europepmc.org/articles/PMC2781300