Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mellisa, Maguire"'
Autor:
Yi Shiau, Ng, Catherine, Feeney, Andrew M, Schaefer, Carol Ellen, Holmes, Paula, Hynd, Charlotte L, Alston, John P, Grady, Mark, Roberts, Mellisa, Maguire, Alexandra, Bright, Robert W, Taylor, Yan, Yiannakou, Robert, McFarland, Doug M, Turnbull, Gráinne S, Gorman
Publikováno v:
Annals of neurology. 80(5)
The m.3243AG MTTL1 mutation is the most common cause of mitochondrial disease; yet there is limited awareness of intestinal pseudo-obstruction (IPO) in this disorder. We aimed to determine the prevalence, severity, and clinical outcome of patients wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d386c671a38545d7aa58a6d2a515eef1
https://pubmed.ncbi.nlm.nih.gov/27804144
https://pubmed.ncbi.nlm.nih.gov/27804144
mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.
Autor:
Grady, John P., Pickett, Sarah J., Ng, Yi Shiau, Alston, Charlotte L., Blakely, Emma L., Hardy, Steven A., Feeney, Catherine L., Bright, Alexandra A., Schaefer, Andrew M., Gorman, Gráinne S., McNally, Richard J. Q., Taylor, Robert W., Turnbull, Doug M., McFarland, Robert
Publikováno v:
EMBO Molecular Medicine; Jun2018, Vol. 10 Issue 6, p1-1, 13p
Autor:
Ng, Yi Shiau, Feeney, Catherine, Schaefer, Andrew M., Holmes, Carol Ellen, Hynd, Paula, Alston, Charlotte L., Grady, John P., Roberts, Mark, Maguire, Mellisa, Bright, Alexandra, Taylor, Robert W., Yiannakou, Yan, McFarland, Robert, Turnbull, Doug M., Gorman, Gráinne S., Gorman, Gráinne S
Publikováno v:
Annals of Neurology; Nov2016, Vol. 80 Issue 5, p686-692, 7p