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pro vyhledávání: '"Helen Finnamore"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-3 (2017)
Abstract Hereditary hemorrhagic telangiectasia (HHT) poses substantial burdens due to nosebleeds and iron deficiency resulting from recurrent hemorrhagic iron losses. Recent studies by our group found surprising links between HHT nosebleeds and certa
Externí odkaz:
https://doaj.org/article/59bfb2cb77f144f7a1b2cdaecc0de769
Autor:
Helen Finnamore, James Le Couteur, Mary Hickson, Mark Busbridge, Kevin Whelan, Claire L Shovlin
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76516 (2013)
BackgroundIron deficiency anemia remains a major global health problem. Higher iron demands provide the potential for a targeted preventative approach before anemia develops. The primary study objective was to develop and validate a metric that strat
Externí odkaz:
https://doaj.org/article/e5dff53e39dc46aea04e6dafe7b14cee
Autor:
Basel Chamali, Kevin Whelan, Mary Hickson, Claire L. Shovlin, Richard A. Manning, Michael Laffan, Helen Finnamore
Publikováno v:
Intractablerare diseases research. 5(2)
Understanding potential provocations of haemorrhage is important in a range of clinical settings, and particularly for people with abnormal vasculature. Patients with hereditary haemorrhagic telangiectasia (HHT) can report haemorrhage from nasal tela
Iron deficiency carries substantial risks, including anaemia and transfusional requirements; suboptimal immune, skeletal muscle, and thyroid function; prematurity; poor maternal and perinatal outcomes in pregnancy; and impaired motor and cognitive de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e34b5bf05465f6d054d9d6283fbdd4d2
https://europepmc.org/articles/PMC3964457/
https://europepmc.org/articles/PMC3964457/
Autor:
Mary Hickson, Helen Finnamore, Claire L. Shovlin, Mark Busbridge, James Le Couteur, Kevin Whelan
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76516 (2013)
PLoS ONE
PLoS ONE
BackgroundIron deficiency anemia remains a major global health problem. Higher iron demands provide the potential for a targeted preventative approach before anemia develops. The primary study objective was to develop and validate a metric that strat
Publikováno v:
Finnamore, H, Silva, B M, Hickson, B M, Whelan, K & Shovlin, C L 2017, ' 7-day weighed food diaries suggest patients with hereditary hemorrhagic telangiectasia may spontaneously modify their diet to avoid nosebleed precipitants ', Orphanet Journal of Rare Diseases, vol. 12, no. 1, 60 . https://doi.org/10.1186/s13023-017-0576-6
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-3 (2017)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-3 (2017)
Orphanet Journal of Rare Diseases
Hereditary hemorrhagic telangiectasia (HHT) poses substantial burdens due to nosebleeds and iron deficiency resulting from recurrent hemorrhagic iron losses. Recent studies by our group found surprising links between HHT nosebleeds and certain food g