Zobrazeno 1 - 6
of 6
pro vyhledávání: '"RUDRAGOUDA S BULAGOUDA"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 6, Pp 01-04 (2024)
Introduction: Alcoholic Liver Disease (ALD) is one of the most significant issues affecting the world today and is the principal cause of atleast 60 of the most significant forms of systemic disorders. The metabolic breakdown of alcohol into acetalde
Externí odkaz:
https://doaj.org/article/ca6cbf6f906442df8651cf6741869af4
Autor:
Smita Hegde, Rajat Hegde, Suyamindra S Kulkarni, Mohd Shannawaz, Kusal K Das, Pramod B Gai, Rudragouda S Bulagouda
Publikováno v:
BLDE University Journal of Health Sciences, Vol 8, Iss 1, Pp 124-129 (2023)
BACKGROUND: In India, hearing loss is a major but often ignored problem. Sixty-three million individuals (6.3%) in India have severe hearing loss. OBJECTIVE: The present study is the first to examine epidemiological factors that are pertinent to chil
Externí odkaz:
https://doaj.org/article/0a455e0ccefe46e18f6903f0798b3657
Autor:
Sujayendra Kulkarni, Rajat Hegde, Smita Hegde, Suyamindra S Kulkarni, Suresh Hanagvadi, Kusal K Das, Sanjeev Kolagi, Pramod B Gai, Rudragouda S Bulagouda
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 11, Iss 6, Pp 2735-2738 (2022)
Background: The most prevalent severe inherited hemorrhagic condition is hemophilia, which means “love of blood.” Hemophilia A and B are caused by a lack or malfunction of the factor VIII and factor IX proteins. Objective: The present study is to
Externí odkaz:
https://doaj.org/article/e6f4e69e89c1416fb5de876a1842b53b
Publikováno v:
JK Science, Vol 24, Iss 1 (2022)
Klinefelter Syndrome is a chromosomal disorder with addition of X sex chromosome (47XXY) in males. A patient attended to our hospital with loss of secondary sexual characteristics and male infertility. Physical examination revealed thin built, hypogo
Externí odkaz:
https://doaj.org/article/1053624784b3471fbfa85ea5b13a13a5
Autor:
Smita Hegde, Rajat Hegde, Suyamindra S. Kulkarni, Kusal K. Das, Pramod B. Gai, Rudragouda S. Bulagouda
Publikováno v:
Global Medical Genetics, Vol 09, Iss 02, Pp 152-158 (2022)
Objective The goal of this research was to investigate the gap junction beta 2 (GJB2) gene mutations associated with nonsyndromic hearing loss individuals in North Karnataka, India. Materials and Methods For this study, patients with sensorineural ge
Externí odkaz:
https://doaj.org/article/a2fb0fdb21e74be5abb2108f0f1a5f82
Publikováno v:
International Journal of Pharma and Bio Sciences. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6efa5545bb20a2d25abc974ce4a30e32
https://doi.org/10.22376/ijpbs.2017.8.2.799-805
https://doi.org/10.22376/ijpbs.2017.8.2.799-805