Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dehannathparambil Kottarathil Vijaykumar"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Background Multiple acyl-CoA dehydrogenase deficiency (MAAD) is a rare metabolic disorder resulting from an abnormality in fatty acid oxidation. There are three types of presentations: neonatal onset with or without congenital anomalies and
Externí odkaz:
https://doaj.org/article/4f98f0bf9dc14d78b3765e8bca41d9fd
Autor:
Dhanya Mary Louis, Dehannathparambil Kottarathil Vijaykumar, Lakshmi Malavika Nair, M. P. Narmadha, Archana George Vallonthaiel, Jyotsna Yesodharan, Renjitha Bhaskaran
Publikováno v:
Indian Journal of Surgical Oncology. 14:208-214
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::177e7c90f58972bf4d5207871dcc9c64
https://doi.org/10.1007/s13193-022-01665-w
https://doi.org/10.1007/s13193-022-01665-w
Autor:
Divya Pillai, Jyoti Narayan, Aleksandra Gentry-Maharaj, Suryanarayana Deo, Dehannathparambil Kottarathil Vijaykumar, Poulome Mukherjee, Nitya Wadhwa, Aparajita Bhasin, Ashutosh Mishra, Anupama Rajanbabu, Ravi Kannan, Zakir Husain, Avinash Kumar, Antonis C. Antoniou, Ranjit Manchanda, Usha Menon
Publikováno v:
Cancers; Volume 15; Issue 11; Pages: 2973
Background: Low awareness of BC and its associated risk factors causes delays in diagnosis and impacts survival. It is critical to communicate BC risk to patients in a format that they are easily able to understand. Our study aim was to develop easy-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56b89d5f3cabc51ad496e42647f50f65
https://www.repository.cam.ac.uk/handle/1810/353424
https://www.repository.cam.ac.uk/handle/1810/353424
Autor:
Kuriakose, Santhosh, Rajan, Anupama, Dehannathparambil Kottarathil, Vijaykumar, Ahmad, Sheikh, Sreehari, Sreekala
Publikováno v:
Indian Journal of Surgical Oncology; Sep2011, Vol. 2 Issue 3, p176-177, 2p