Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Anna M. Branstad"'
Autor:
Melissa M. Harrison, Catherine A. Fox, Anna M. Branstad, Stephen L. McDaniel, Marissa M Gaskill, Allison J. Hollatz
Publikováno v:
Genetics
Meier-Gorlin syndrome (MGS) is a recessive disorder caused by mutations in genes associated with DNA replication. Despite the fact these proteins are essential for replication in every cell, patients with MGS have tissue-specific defects...
Meie
Meie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f6037f53d201495bbc7d44a640cdb32
https://doi.org/10.1534/genetics.119.302938
https://doi.org/10.1534/genetics.119.302938
Autor:
Lindsay R Hunter Guevara, Jason S. Eldrige, Laura Matzke Bitterman, Matthew J. Pingree, Wayne T. Nicholson, Anna M. Branstad, Lindsay L. Warner
Publikováno v:
Journal of Medical Case Reports, Vol 14, Iss 1, Pp 1-4 (2020)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Sufentanil is a potent opioid uncommonly used to manage pain and is rarely administered via an intrathecal pain pump system. Case presentation This case illustrates the use of intrathecal sufentanil in a 50-year-old Caucasian man for the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6cb5de46b3ecc5bb857c297c62b0c09
https://doaj.org/article/6351fabc7ac34311a4450186ab2e519e
https://doaj.org/article/6351fabc7ac34311a4450186ab2e519e
Autor:
Anna M. Branstad, Melissa M. Harrison, Stephen L. McDaniel, Catherine A. Fox, Allison J. Hollatz
Meier-Gorlin syndrome is a rare recessive disorder characterized by a number of distinct developmental defects, including primordial dwarfism, small ears, and small or missing patella. Genes encoding members of the origin recognition complex (ORC) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d82c85cf4213923123d928a3ac35798
https://doi.org/10.1101/711820
https://doi.org/10.1101/711820
