Zobrazeno 1 - 7
of 7
pro vyhledávání: '"G S, Kadakol"'
Publikováno v:
International Journal of Clinical and Biomedical Research. :37-40
Objective: Down syndrome is a common genetic disease, diagnosed with congenital malformation/mental retardation. Down syndrome occurs in all races & economic levels. It is caused by third copy of chromosome 21, there are there forms of DS. Simple Tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a5e8a0ce21090e5e13981428fcc8935
https://doi.org/10.31878/ijcbr.2018.51.10
https://doi.org/10.31878/ijcbr.2018.51.10
Publikováno v:
International Journal of Pharma and Bio Sciences. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5b9d492a19f07c59bc4f1af699cd432
https://doi.org/10.22376/ijpbs.2017.8.2.b27-30
https://doi.org/10.22376/ijpbs.2017.8.2.b27-30
Autor:
Suyamindra S. Kulkarni, Kumarasamy Thangaraj, Jayaraj Sindhoor, S.V. Hiremath, Pramod B. Gai, Suresh Basavraj, Bhushan B. Kulkarni, Vandana T, Amruta Markande, G S Kadakol
Publikováno v:
Asian Journal of Medical Sciences, Vol 2, Iss 2, Pp 82-86 (2011)
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal dominant trait characterized by an increased plasma low-density lipoprotein (LDL) level. The disease is caused by several different mutations in the LDL r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc2b3a8bb6e47b815daaba56d20ef6a
https://doi.org/10.3126/ajms.v2i2.4573
https://doi.org/10.3126/ajms.v2i2.4573
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. 10:3
Turner syndrome (TS) is a common chromosomaldisorder. Turner syndrome (TS) also known as Ulrich–Turner syndrome, gonadal dysgenesis and 45, X, is a condition in which a female is partly or completely missing an X chromosome.The main clinical featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a0b741e9f9df6332a2f28330e5eed35
https://doi.org/10.22159/ajpcr.2017.v10i4.16484
https://doi.org/10.22159/ajpcr.2017.v10i4.16484
Autor:
Suyamindra S, Kulkarni, Sujayendra S, Kulkarni, Priyanka P, Vastrad, Bhushan B, Kulkarni, Amruta R, Markande, G S, Kadakol, S V, Hiremath, S, Kaliwal, B R, Patil, Pramod B, Gai
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 12(3)
In view of conducting HPV vaccination in India it is most important to understand the prevalence of HPV genotypes in this population, not only in squamous cell carcinoma of cervix and oral cavity but also in the general population. In this study we e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::18fd8cef1653d973657e9da68f6b76fe
https://pubmed.ncbi.nlm.nih.gov/21627358
https://pubmed.ncbi.nlm.nih.gov/21627358
Autor:
Harendra, Modak, Suyamindra S, Kulkarni, G S, Kadakol, S V, Hiremath, B R, Patil, Umesh, Hallikeri, Pramod B, Gai
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 12(3)
The aim of this study was to analyze the trends in the incidence rates of four major types of leukemia in the population of North Karnataka, which accounts for the 2.5% of the whole population of India. Due to the lack of any nationwide leukemia scre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::294948d874b2db0acaa2fa449070ecbb
https://pubmed.ncbi.nlm.nih.gov/21627362
https://pubmed.ncbi.nlm.nih.gov/21627362
Publikováno v:
Neurology India. 62:149
Background: Parkinson's disease (PD) is a disabling neurological disorder characterized by progressive degeneration of dopaminergic neurons. Mutations analysis within the α-synuclein gene (SNCA) on chromosome 4 has been reported in the last decade.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6670ab9faaa12d66c775966598c7adbc
https://doi.org/10.4103/0028-3886.132338
https://doi.org/10.4103/0028-3886.132338