Zobrazeno 1 - 10
of 93
pro vyhledávání: '"MANDAVA V RAO"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 3, Pp GE01-GE09 (2021)
Introduction: Infertility affects about 15% of couples attempting pregnancy and in approximately 50% of these cases, male factors are responsible. Male infertility is clinically characterised by azoospermia and oligozoospermia depending on the amo
Externí odkaz:
https://doaj.org/article/bbfa0a60f10649dcb31ed91d47519fa4
Autor:
Sandip C Shah, Nidhi D Shah, Parth S Shah, Hari Shankar P Ray, Ketan K Vaghasia, Anil K Mehta, Bhavini S Shah, Mandava V Rao
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 8, Pp GC05-GC10 (2019)
Introduction: Among all chromosomes (46) in the human genome, particular significance has been given to chromosomes 13, 18, 21, X and Y. This is primarily because of aneuploidy in these chromosomes that result in viable pregnancies with congenital de
Externí odkaz:
https://doaj.org/article/6ad62cd54d394553bd6315391ac261be
Autor:
Parth S Shah, Nidhi D Shah, Hari Shankar P Ray, Nikunj B Khatri, Ketan K Vaghasia, Mandava V Rao, Sandip C Shah
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 5, Pp GC01-GC06 (2018)
Introduction: The β-thalassaemia is one of the haemoglobinopathies related to genetic disorders. It occurs due to mutation in β-gene of autosome 11. In India, it affects 1-7% of couples annually. Reports are available in few states of India about
Externí odkaz:
https://doaj.org/article/0747a224ff7d45dc892a48ae334fe426
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, Pp GD01-GD03 (2017)
The mutations in Haemoglobin Beta (HBB) gene, bring about less or no production of Hb β-chain synthesis in affected cases, leading from minor to major types depending on haematological indices. In compound heterozygotic conditions, two traits are
Externí odkaz:
https://doaj.org/article/898f384fa5e344c6973dbd8281537c3a
Publikováno v:
Annals of Indian Academy of Neurology, Vol 17, Iss 3, Pp 303-307 (2014)
Objective: In India, various groups have studied different regions to find out deletion pattern of dystrophin gene. We have investigated its deletion pattern among Duchenne/Becker muscular dystrophy (D/BMD) patients across Gujarat. Moreover, in this
Externí odkaz:
https://doaj.org/article/a8dbc527dc74474883e47763f9bbd507
Autor:
Nidhi P Shah, Krishna Mistry, Mudra Kansara, K Sonali, Nirali Thakkar, Parth S Shah, Sandip C Shah, Mandava V Rao
Publikováno v:
Eastern Journal of Medical Sciences. :61-65
Introduction: Male infertility (MI) in about 50% of couples is constituted due to genetic, hormonal, and epigenetic factors. Almost 10% of it is contributed to genetic anomalies. Objectives: This study was undertaken in 787 males with infertility and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1994ad8869be2e2654ba1c97da3f28b5
https://doi.org/10.32677/ejms.v6i4.3220
https://doi.org/10.32677/ejms.v6i4.3220
Autor:
Shradha Mehta, Bhavana Mehta, Sandip Shah, Sanjay Vyas, Raksha Sharma, Saifali Agarwal, MANDAVA V RAO
Publikováno v:
Indian Journal of Case Reports. :55-57
Hydatid disease is caused by the adult and the larval stage of tapeworms belonging to the Echinococcus species. The major sites of its infection are the liver and lungs. Rarely, it affects the pelvic region including the ovary, accounting for 0.2–2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fe7af59b5dd61b38cf913d9640bc25e
https://doi.org/10.32677/ijcr.v8i3.3310
https://doi.org/10.32677/ijcr.v8i3.3310
Publikováno v:
Eastern Journal Of Medical Sciences. 6:1-8
Background: Y chromosome microdeletions provide a pivotal role in the control of spermatogenesis. These are located on the q arm of it, specifically, the azoospermia factor (AZF) region, hence named as Yq microdeletions. The mutations in this region
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1112313d092a55b89237375f3e0267f7
https://doi.org/10.32677/ejms.2021.v06.i01.001
https://doi.org/10.32677/ejms.2021.v06.i01.001
Autor:
Mandava V. Rao, Parth S Shah, Jeanny Dominic, Rutvik J Raval, Tapan A Patel, Sandip C Shah, Nidhi P Shah
Publikováno v:
Eastern Journal Of Medical Sciences. :19-21
Background: Y chromosome microdeletions are one of the genetic causes of male infertility. Evaluation of this is important clinically to assist couple with such genetic defects using polymerase chain reaction-based sequence-targeted-site (STS). Objec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e32eb33fe2b6f876ab291a7d8067893c
https://doi.org/10.32677/ejms.2020.v05.i01.006
https://doi.org/10.32677/ejms.2020.v05.i01.006
Autor:
Mandava V. Rao, Koya Prabhakara Rao, Reddymasu Sreenivasulu, Madala Subramanyam, Rambabu Gundla
Publikováno v:
Letters in Drug Design & Discovery. 15:1299-1307
Background: Hetero atom containing compounds are well studied class of organic compounds exhibits variety of properties and applications. Design and synthesis of new heterocyclic compounds are always of great interest in synthetic and medicinal organ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23f60f8afcb3a29107e0dd73943dc9f4
https://doi.org/10.2174/1570180815666180219165119
https://doi.org/10.2174/1570180815666180219165119