Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Melissa Sheehan"'
Autor:
Anastasia Ambrose, Melissa Sheehan, Shalini Bahl, Taryn Athey, Shailly Ghai-Jain, Alicia Chan, Saadet Mercimek-Andrews
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-14 (2022)
Abstract Background Mitochondrial long-chain fatty acid oxidation and carnitine metabolism defects are a group of inherited metabolic diseases. We performed a retrospective cohort study to report on the phenotypic and genotypic spectrum of mitochondr
Externí odkaz:
https://doaj.org/article/6e097366b4a24929b021bb1bf5bea47a
Publikováno v:
JIMD Reports, Vol 55, Iss 1, Pp 32-37 (2020)
Abstract Refsum disease is a rare inherited metabolic disorder arising from a defect in peroxisomal metabolism. Patients lack the functional enzyme phytanoyl‐CoA hydroxylase, resulting in perturbed alpha oxidation of fatty acids. Phytanic acid accu
Externí odkaz:
https://doaj.org/article/a2f2ae7b9b1e4797a6771ea0ef181346
Publikováno v:
Nutrition in Clinical Practice. 30:111-116
This study aimed to determine the prevalence of inadequate serum 25-hydroxyvitamin D (25(OH)D) levels in a pediatric Canadian cystic fibrosis (CF) population and to assess the effectiveness of a vitamin D supplementation protocol on improving vitamin
Publikováno v:
Journal of Pediatric Care. 2
Background: Comparison of estimated energy requirements using predictive equations (PBMR) to measured resting energy requirements (MREE) using indirect calorimetry is not widely investigated in the pediatric lung transplant (LTx) population. In this
Publikováno v:
Cell communicationadhesion. 8(4-6)
Innexins are functionally analogous to the vertebrate connexins, and the innexin family of gap junction proteins has been identified in many invertebrates, including Drosophila and C. elegans. The genome sequencing project has identified 25 innexins
Autor:
Ambrose, Anastasia1 (AUTHOR), Sheehan, Melissa1 (AUTHOR), Bahl, Shalini2,3 (AUTHOR), Athey, Taryn1 (AUTHOR), Ghai-Jain, Shailly1 (AUTHOR), Chan, Alicia1 (AUTHOR), Mercimek-Andrews, Saadet1 (AUTHOR) saadet@ualberta.ca
Publikováno v:
Orphanet Journal of Rare Diseases. 9/15/2022, Vol. 17 Issue 1, p1-14. 14p.
Publikováno v:
Social Sciences & Humanities Studies / Društvene i Humanističke Studije (DHS); 2023, Vol. 8 Issue 2, p791-809, 19p
Publikováno v:
Journal of Inherited Metabolic Disease Reports; Sep2020, Vol. 55 Issue 1, p32-37, 6p
Autor:
PR Newswire
Publikováno v:
PR Newswire US. 10/24/2023.
Publikováno v:
Nutrition in Clinical Practice; Feb2015, Vol. 30 Issue 1, p111-116, 6p