Zobrazeno 1 - 10
of 35
pro vyhledávání: '"B., MANEESHA"'
Publikováno v:
i-Manager's Journal on Digital Signal Processing; Jun2024, Vol. 12 Issue 1, p15-20, 6p
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
Publikováno v:
2022 2nd International Conference on Artificial Intelligence and Signal Processing (AISP).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c861b126faa84630d2046edcc17fc4cc
https://doi.org/10.1109/aisp53593.2022.9760688
https://doi.org/10.1109/aisp53593.2022.9760688
Autor:
B. Maneesha
Publikováno v:
International Journal of Pure & Applied Bioscience. 7:399-404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15fc3796296aa418f10cb3321bb9d90d
https://doi.org/10.18782/2320-7051.7720
https://doi.org/10.18782/2320-7051.7720
Autor:
B. Maneesha
Publikováno v:
International Journal of Pure & Applied Bioscience. 7:364-371
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e09b436e90a328ef79b1d12f6da221e
https://doi.org/10.18782/2320-7051.7647
https://doi.org/10.18782/2320-7051.7647
Publikováno v:
Lecture Notes in Networks and Systems ISBN: 9789811582172
Nowadays, researchers are trying to reveal better consequences by acting on machine learning (ML) algorithms. The notion behind this study is to represent the fundamental machine learning algorithms and its applicability in current scenario. Backprop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee8bb3797c36de8104a30b5a5199e888
https://doi.org/10.1007/978-981-15-8218-9_25
https://doi.org/10.1007/978-981-15-8218-9_25
Autor:
Finnamore, Helen1,2, Silva, B. Maneesha3, Hickson, B. Mary4, Whelan, Kevin2, Shovlin, Claire L.1,5 c.shovlin@imperial.ac.uk
Publikováno v:
Orphanet Journal of Rare Diseases. 3/28/2017, Vol. 12, p1-3. 3p.
Publikováno v:
Orphanet Journal of Rare Diseases
Background Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. Life expectancy is surprisingly good, particularly f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f28af415659eeee13d68bcece083a00a
https://doi.org/10.1186/1750-1172-8-195
https://doi.org/10.1186/1750-1172-8-195
Publikováno v:
The Laryngoscope. 123(5)
Objectives/Hypothesis To identify factors influencing the severity of epistaxis in hereditary hemorrhagic telangiectasia (HHT). Study Design Participants with and without HHT were recruited from a specialist service and online following advertisement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63aec04ce36fca49f600da689ed69acb
https://pubmed.ncbi.nlm.nih.gov/23404156
https://pubmed.ncbi.nlm.nih.gov/23404156
Publikováno v:
The Lancet. 383:S40
Background Thrombotic disease is usually treated with anticoagulant or antiplatelet agents, but the presence of a haemorrhagic disorder restricts anticoagulant use in many National Health Service Trust guidelines, including our own. Hereditary haemor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a785b46ad45f53fa316336b87c4f9f4
https://doi.org/10.1016/s0140-6736(14)60303-2
https://doi.org/10.1016/s0140-6736(14)60303-2