Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Ariachery C. Ammini"'
Autor:
Sachin Chittawar, Saptarshi Bhattacharya, Jai Prakash Sahoo, Siva Prakash, Ashu Seith Bhalla, Devasenathipathy Kandasamy, Arundeep Arora, Nandita Gupta, Nikhil Tandon, Ravinder Goswami, Rajesh Khadgawat, Viveka P Jyotsna, Ashish Kumar Karak, Chandra Sekhar Bal, Ravindra Mohan Pandey, Guresh Kumar, Ariachery C Ammini
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 1, Pp 128-132 (2013)
Background: Demonstration of central: Peripheral adrenocorticotropic hormone (ACTH) gradient is important for diagnosis of Cushing′s disease. Aim: The aim was to assess the utility of internal jugular vein (IJV): Peripheral vein ACTH ratio for diag
Externí odkaz:
https://doaj.org/article/3e7d13010d9043f2b9ac5a8289a68e3f
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 6, Pp 972-975 (2012)
Aim of Study: To assess the utility of internal jugular vein (IJV) / peripheral adrenocorticotropic hormone (ACTH) gradient in determining the etiology of ACTH- dependent Cushing′s syndrome. Materials and Methods: Patients with ACTH-dependent Cushi
Externí odkaz:
https://doaj.org/article/b3eab23dead74013b85d4499fe227adc
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 3, Pp 395-399 (2012)
Background: Some boys with sexual precocity are known to have behavioral problems like increased physical and verbal aggression and school and social maladjustments. It is believed to be due to premature androgen exposure. However, it is not clear wh
Externí odkaz:
https://doaj.org/article/5e8d29fd4a48449ba41803074c059994
Autor:
Eunice Marumudi, Arundhati Sharma, Bindu Kulshreshtha, Rajesh Khadgawat, Madan L Khurana, Ariachery C Ammini
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 3, Pp 384-388 (2012)
Context: Congenital adrenal hyperplasia (CAH) is one of the inborn errors of metabolic disorder inherited in an autosomal recessive manner caused by the defects in the steroid 21 hydroxylase CYP21A2 gene. We analyzed the genotype of 62 patients with
Externí odkaz:
https://doaj.org/article/f5c86b6405814da6be263103afa3988d
Autor:
Edavan P Praveen, Jayaprakash Sahoo, Madan L Khurana, Bindu Kulshreshtha, Rajesh Khadgawat, Nandita Gupta, Sada Nand Dwivedi, Guresh Kumar, Dorairaj Prabhakaran, Ariachery C Ammini
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 1, Pp 105-111 (2012)
Aims: The aim was to study the effect of family history of type 2 diabetes mellitus (T2DM) on insulin sensitivity and b-cell function in normoglycemic offspring. Material and Methods: Offspring of T2DM patients (cases) and individuals without family
Externí odkaz:
https://doaj.org/article/efa060ff9e31466e9c5891ad9789bb14
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 4, Pp 599-603 (2012)
Introduction: Children with congenital adrenal hyperplasia (CAH) provide us an opportunity to study the clinical effects of androgen excess in humans. We studied the sequence of pubertal development in girls with congenital adrenal hyperplasia initia
Externí odkaz:
https://doaj.org/article/627b2d73f41f446ab26088ea2a5f8833
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 15, Iss 1, Pp 38-42 (2011)
Background: The pathogenesis of type 1 diabetes mellitus (T1DM) requires a genetic predisposition to particular environmental triggers that may activate mechanisms leading to progressive loss of pancreatic beta cells. Aims: We tried to compare the im
Externí odkaz:
https://doaj.org/article/ffe3da04074a42b09402d7a73cd97825
Autor:
Marumudi Eunice, Ariachery C Ammini
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 3, Pp 373-375 (2013)
Management of congenital adrenal hyperplasia (CAH) from embryonic stage to adulthood is a critical challenge. We would like to comment on some of the practical difficulties in offering prenatal treatment for CAH-affected fetuses in Indian population.
Externí odkaz:
https://doaj.org/article/2f6a8939fd38468aa55ce63e1008de9f
Autor:
Deepak Khandelwal, Saptarshi Bhattacharya, Rajesh Khadgawat, Satbir Kaur, Nikhil Tandon, Ariachery C Ammini
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 5, Pp 853-855 (2012)
Primary Sjögren′s syndrome (pSS) is a chronic autoimmune disease characterized by a progressive lymphocytic infiltration of the exocrine glands with varying degrees of systemic involvement. Overt or latent renal tubular acidosis (RTA), caused by t
Externí odkaz:
https://doaj.org/article/96e49c35ca0c4f3bbe5f24cf646bfb14
Autor:
Yashdeep Gupta, Ariachery C Ammini
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 3, Pp 463-465 (2012)
Vitiligo in association with autoimmune endocrine disorders, especially with hypothyroidism, is not uncommon. Some amount of pericardial effusion is usually present in long-standing/untreated hypothyroidism. Here we describe the case of young male wi
Externí odkaz:
https://doaj.org/article/4d93ca345ed74ef99b39a1993d2a32a2