Zobrazeno 1 - 10
of 48
pro vyhledávání: '"M Sriharibabu"'
Autor:
G. Leela Jaya Madhuri, M Sriharibabu, Somanath Das, Y Himabindu, D Kiranmai, R K Chaitanya Reddy
Publikováno v:
Journal of Clinical and Scientific Research, Vol 7, Iss 3, Pp 119-123 (2018)
Background: Chronic Obstructive Pulmonary Disease (COPD) is one of the major non-communicable diseases associated with increased morbidity and mortality. Even though COPD is a systemic disorder with the predominant involvement of lungs, several co-mo
Externí odkaz:
https://doaj.org/article/7e0803f440204b5590f2de267a5a11df
Publikováno v:
Journal of Human Reproductive Sciences, Vol 6, Iss 1, Pp 27-31 (2013)
Objective: The objective of this study was to test the hypothesis that AMH and antral follicle count (AFC) are good predictors of ovarian response to controlled ovarian stimulation and to compare them. Materials and Methods: This observational cross-
Externí odkaz:
https://doaj.org/article/410ec32bb86f4c0188595bfb4261145e
Publikováno v:
Journal of Human Reproductive Sciences, Vol 7, Iss 3, Pp 221-223 (2014)
Complete Androgen insensitivity syndrome is a disorder of hormone resistance characterized by a female phenotype in an individual with an XY karyotype. The pathogenesis of CAIS involves a defective androgen receptor gene located on X-chromosome at Xq
Externí odkaz:
https://doaj.org/article/69c3cd2cfe81472bb02bd4fe0538e99f
Autor:
Dr. M. Sriharibabu, M.D.
Publikováno v:
Indian Heart Journal, Vol 68, Iss 4, Pp 445-446 (2016)
Externí odkaz:
https://doaj.org/article/06cd12d32fa44f3f97fc7958e5d76287
Autor:
YS Sarma, M Sriharibabu
Publikováno v:
The Indian Journal of Medical Research
Indian Journal of Medical Research, Vol 150, Iss 3, Pp 310-311 (2019)
Indian Journal of Medical Research, Vol 150, Iss 3, Pp 310-311 (2019)
Publikováno v:
Journal of Clinical and Scientific Research, Vol 4, Iss 4, Pp 296-300 (2015)
Gardners syndrome (GS) is a variant of familial adenomatous polyposis (FAP) and presents with both colonic and extra colonic manifestations. It is an autosomal dominant disorder and results from mutations in adenomatous polyposis coli (APC) gene. Pat
Publikováno v:
Journal of Clinical and Scientific Research, Vol 4, Iss 3, Pp 227-231 (2015)
Turcot’s syndrome is a rare genetic disorder clinically characterised by concomitant occurrence of primary brain tumour and colorectal polyposis. It is commonly seen in association with two other syndromes, namely, hereditary nonpolyposis colorecta
Publikováno v:
The Indian Journal of Medical Research
Indian Journal of Medical Research, Vol 139, Iss 2, Pp 267-272 (2014)
Indian Journal of Medical Research, Vol 139, Iss 2, Pp 267-272 (2014)
Background & objectives: Uterine leiomyomas (fibroids) are common cause of morbidity in women of reproductive age group. High intensity focused ultrasound with the imaging guidance of magnetic resonance imaging (MRI) known as magnetic resonance guide
Autor:
M. Sriharibabu, K. Subhramanyam, T. Sivakumar, D.J.K. Chakravarthy, K. Chandrakanth, Y.S. Sarma
Publikováno v:
Journal of Indian College of Cardiology. 3:134-138
The Bardet–Biedl syndrome (BBS) is a rare genetically heterogeneous, autosomal recessive inherited disorder with wide variability in expression. BBS presents with varied clinical manifestations like retinitis pigmentosa, post axial polydactyly, cen
Publikováno v:
Journal of Human Reproductive Sciences, Vol 7, Iss 3, Pp 221-223 (2014)
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences
Complete Androgen insensitivity syndrome is a disorder of hormone resistance characterized by a female phenotype in an individual with an XY karyotype. The pathogenesis of CAIS involves a defective androgen receptor gene located on X-chromosome at Xq