Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Muneer Kader"'
Publikováno v:
Saudi Journal of Medicine and Medical Sciences, Vol 2, Iss 3, Pp 229-231 (2014)
Hereditary hemochromatosis is an inherited condition of dysregulated iron absorption, and usually presents with clinical features of hepatic dysfunction. Cardiac involvement as the presenting manifestation of hereditary hemochromatosis is rare. We re
Externí odkaz:
https://doaj.org/article/4679fdb362bf4ec19af502263ec1b2d5
Publikováno v:
Indian Heart Journal, Vol 67, Iss 3, Pp 266-267 (2015)
Bicuspid aortic valve is the most common congenital cardiac malformation, affecting 1%–2% of the population. Among various complications, incidence of infective endocarditis (IE) in the bicuspid aortic valve population is high with higher rate of p
Externí odkaz:
https://doaj.org/article/54810d3f9b4644cf84473a169eb8229f
Autor:
Muneer, Kader1, Jose, Benny2 drbennyjose@gmail.com, Dubey, Gajendra2, T., Ajayakumar1, C. G., Sajeev1, M. N., Krishnan1
Publikováno v:
European Journal of Breast Health. Oct2022, Vol. 18 Issue 4, p299-305. 7p.
Autor:
Muneer, Kader, Nair, Anishkumar
Publikováno v:
In Indian Heart Journal May-June 2017 69(3):371-374
Autor:
Rajesh, Gopalan Nair, Sajeer, Kalathingathodika, Sajeev, Chakanalil Govindan, Bastian, Cicy, Vinayakumar, Desabandhu, Muneer, Kader, Haridasan, Vellani, Mathew, Dolly, George, Biju, Krishnan, Mangalath Narayanan
Publikováno v:
In Indian Heart Journal May-June 2016 68(3):311-315
Publikováno v:
Heart India; Jan-Apr2024, Vol. 12 Issue 1, p40-46, 7p
Autor:
Rajesh, Gopalan Nair, Raju, Deepak, Nandan, Deepak, Haridasan, Vellani, Vinayakumar, Desabandhu, Muneer, Kader, Sajeev, C.G., Babu, Kadangot, Krishnan, M.N.
Publikováno v:
In Indian Heart Journal September-October 2013 65(5):522-528
Autor:
Haridasan, Vellani, Nandan, Deepak, Raju, Deepak, Rajesh, Gopalan Nair, Sajeev, C.G., Vinayakumar, Desabandhu, Muneer, Kader, Babu, Kadangot, Krishnan, M.N.
Publikováno v:
In Indian Heart Journal March-April 2013 65(2):142-146
Publikováno v:
In IHJ Cardiovascular Case Reports (CVCR) January-April 2017 1(1):48-50
Akademický článek
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