Zobrazeno 1 - 10 of 57 pro vyhledávání: '"Mamatha Gs"'
1
Akademický článek
A Narrative Review on the Conceptual and Methodological Advancements in Digital Disruption: A Way to Improved Quality of Services in Health Care
Autor: Devika Kanade, Shailendrakumar Kale, Mamatha GS Reddy, Ankita Mathur
Publikováno v: Health Technology Assessment in Action, Vol 8, Iss 4 (2024)
Background: The adoption and successful implementation of digital health solutions heavily depend on digital health literacy, which is particularly critical in the current COVID-19 era. Low levels of digital health literacy are associated with poor p
Externí odkaz: https://doaj.org/article/adc1d704b7874bdda81b5397c3d78597
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2
Akademický článek
Mast cell mediated myofibroblast differentiation responsible for progression of oral submucous fibrosis
Autor: Mamatha GS Reddy, Pradnya Kakodkar, Vini Mehta
Publikováno v: Oral Oncology Reports, Vol 9, Iss , Pp 100216- (2024)
Myofibroblast from ally to adversary confirmed the role of myofibroblast in the progression of OSF. Several theories have been postulated regarding the etiopathogenesis of OSF, fibroblast being the key cell in causing fibrosis mediated by TGF. Howeve
Externí odkaz: https://doaj.org/article/4aaa79d5b7264ca5af0aa234a1f7b1ca
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3
Akademický článek
Enigmatic Morpho-Insight: Toto bodies
Autor: Mamatha GS Reddy, Supriya Kheur
Publikováno v: Medical Journal of Dr. D.Y. Patil University, Vol 8, Iss 1, Pp 121-122 (2015)
Externí odkaz: https://doaj.org/article/d937995c0e594f518048a38b0104e9a1
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4
Akademický článek
Correlation of Stature with Incisoapical Length of Anterior Teeth Using Cone-Beam Computed Tomography (CBCT).
Autor: Shinde, Aditi, Reddy, Mamatha GS, Gawali, Rohan
Publikováno v: Journal of Health & Allied Sciences NU; Oct2024, Vol. 14 Issue 4, p448-452, 5p
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6
Apert’s Syndrome: Report of a New Case and its Management
Autor: Shweta Dixit, Asha Singh, Prashant P. Jaju, Rajiv S Desai, Mamatha Gs
Publikováno v: International Journal of Clinical Pediatric Dentistry
In this article, an interesting case of Apert syndrome in a 14-year-old boy with characteristic craniosynostosis, acrocephaly, midface hypoplasia, pharyngeal attenuation, ocular manifestations, and syndactyly of the hands and feet is presented. The c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4d262da9452cf3bfc9c75f7da1dcc36
http://europepmc.org/articles/PMC4086543
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Plný text Recenzováno Digitální knihovna AV ČR
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