Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nelsan Pourhadi"'
Autor:
Christian Torp-Pedersen, Lina Steinrud Mørch, Nelsan Pourhadi, Amani Meaidi, Ellen Christine Løkkegaard
Publikováno v:
BMJ Medicine, Vol 3, Iss 1 (2024)
Objective To estimate the rate of breast cancer associated with use of vaginal oestradiol tablets according to duration and intensity of their use.Design Registry based, case-control study, nested in a nationwide cohort.Setting Based in Denmark using
Externí odkaz:
https://doaj.org/article/372a661ae07f4a2a9edf96ec959949c8
Publikováno v:
PLoS Medicine, Vol 20, Iss 12, p e1004321 (2023)
BackgroundUse of estrogen-containing menopausal hormone therapy has been shown to influence the risk of central nervous system (CNS) tumors. However, it is unknown how the progestin-component affects the risk and whether continuous versus cyclic trea
Externí odkaz:
https://doaj.org/article/b1bb059f6a844a0e8f87f837e79d1f79
Autor:
Tobias Melton Axelsen, Tzvetelina Lubenova Vammen, Mads Bak, Nelsan Pourhadi, Christian Midtgaard Stenør, Sabine Grønborg
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 28, Iss , Pp 100782- (2021)
Background: Mitochondrial alanyl-tRNA synthetase 2 gene (AARS2) related disease is a rare genetic disorder affecting mitochondrial metabolism, leading to severe cardiac disease in infants or progressive leukodystrophy in young adults. The disease is
Externí odkaz:
https://doaj.org/article/1cdb0af695f94429a8431d77930adec4
Autor:
Pourhadi, Nelsan1,2 (AUTHOR) pourhadi@regionh.dk, Meaidi, Amani2 (AUTHOR), Friis, Søren2 (AUTHOR), Torp-Pedersen, Christian3,4 (AUTHOR), Mørch, Lina S.2 (AUTHOR)
Publikováno v:
PLoS Medicine. 12/19/2023, Vol. 20 Issue 12, p1-16. 16p.
Autor:
Mads Bak, Nelsan Pourhadi, Christian Stenör, Sabine Grønborg, Tobias Melton Axelsen, Tzvetelina Lubenova Vammen
Publikováno v:
Molecular Genetics and Metabolism Reports
Axelsen, T M, Vammen, T L, Bak, M, Pourhadi, N, Stenør, C M & Grønborg, S 2021, ' Case report : ‘AARS2 leukodystrophy’ ', Molecular Genetics and Metabolism Reports, vol. 28, 100782 . https://doi.org/10.1016/j.ymgmr.2021.100782
Molecular Genetics and Metabolism Reports, Vol 28, Iss, Pp 100782-(2021)
Axelsen, T M, Vammen, T L, Bak, M, Pourhadi, N, Stenør, C M & Grønborg, S 2021, ' Case report : ‘AARS2 leukodystrophy’ ', Molecular Genetics and Metabolism Reports, vol. 28, 100782 . https://doi.org/10.1016/j.ymgmr.2021.100782
Molecular Genetics and Metabolism Reports, Vol 28, Iss, Pp 100782-(2021)
Background Mitochondrial alanyl-tRNA synthetase 2 gene (AARS2) related disease is a rare genetic disorder affecting mitochondrial metabolism, leading to severe cardiac disease in infants or progressive leukodystrophy in young adults. The disease is c
Publikováno v:
Ugeskrift for laeger. 183(23)
Chronic traumatic encephalopathy (CTE) is associated with a history of repetitive head impacts, such as those sustained through contact sports. Post-mortem assessment has revealed specific neuropathological characteristics related to the condition. T
Publikováno v:
Alzheimer'sdementia : the journal of the Alzheimer's AssociationREFERENCES. 18(4)
Use of systemic hormone therapy has been positively associated with development of dementia. Little is known about the dose-dependent effect of vaginal estradiol on dementia risk.We assessed associations between cumulative dose of vaginal estradiol t
Publikováno v:
JAMA: Journal of the American Medical Association; 5/14/2024, Vol. 331 Issue 18, p1594-1596, 3p
Publikováno v:
BMJ: British Medical Journal; 8/19/2023, Vol. 382 Issue 8395, pp1776-p1776, 1p
Publikováno v:
European Journal of Neurology; Sep2023, Vol. 30 Issue 9, p2811-2820, 10p