Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mark McIlduff"'
Autor:
Harvey L. Levy, Deborah Kinch, Jessica Lindenberger, Mark McIlduff, Sarah Hawthorne, Jerry Vockley, Vera Anastosoaie, Diana Lamppu, Albert B. Seymour, Sharon Watling, Kevin DiBona, Jennifer L. Baker
Publikováno v:
Molecular genetics and metabolism. 129(3)
Phenylketonuria (PKU) is an autosomal recessive disease caused by mutations in the PAH gene, resulting in deficiency of phenylalanine hydroxylase (PAH), an enzyme that converts phenylalanine (Phe) to tyrosine (Tyr). The purpose of this study was to c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d379968a69266c6b45eff77dbd43b1
https://pubmed.ncbi.nlm.nih.gov/31883647
https://pubmed.ncbi.nlm.nih.gov/31883647
Autor:
Douglas P, Beall, Jeffrey D, Coe, Mark, McIlduff, Daniel, Bloch, John, Hornberger, Christopher, Warner, Sean, Tutton
Publikováno v:
Pain physician. 20(6)
The KAST (Kiva Safety and Efficacy) investigation device exempt (IDE) study indicated that the majority of patients responded equally well to vertebral augmentation using either an implant-based approach or balloon kyphoplasty (BK). Additional invest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dfa7ff8066d4024ec32364796526e553
https://pubmed.ncbi.nlm.nih.gov/28934783
https://pubmed.ncbi.nlm.nih.gov/28934783
Autor:
Debby Holmes Higgin, Douglas P. Beall, Jeffrey D. Coe, Mark McIlduff, Daniel Bloch, Qianyi Li, Sean Tutton, John Hornberger
Publikováno v:
The Spine Journal. 16:S120-S121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da94a44cb45ac3295cb5bd2e327a6cc
https://doi.org/10.1016/j.spinee.2016.07.012
https://doi.org/10.1016/j.spinee.2016.07.012