Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Rajeev Philip"'
Autor:
Sanjay Saran, Bharti Sona Gupta, Rajeev Philip, Kumar Sanjeev Singh, Sureshrao Anoop Bende, Puspalata Agroiya, Pankaj Agrawal
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 20, Iss 1, Pp 108-113 (2016)
Objective: Objective was to evaluate reproductive hormones levels in hypothyroid women and impact of treatment on their levels. Materials and Methods: A total of 59 women with untreated primary hypothyroidism were included in this prospective study.
Externí odkaz:
https://doaj.org/article/425ab72b9aa144dfa74b7347de22513c
Autor:
Rajeev Philip, Sarojini Amma Cheradiyil Sivaraman Nair, Varkey Kuruvilla, Shalu Mariam John, Dev Amal, Keshavan Charamel Sankaran
Publikováno v:
CHRISMED Journal of Health and Research, Vol 3, Iss 3, Pp 203-206 (2016)
Context: Thyrotoxicosis is a common clinical problem, and the most common cause of thyrotoxicosis is Graves′ disease and is 4 times more common than the other causes combined. Of late, the number of people incidentally detected to have biochemical
Externí odkaz:
https://doaj.org/article/5bc392c608364c0997a98386764b0b35
Autor:
Pankaj Agrawal, Rajeev Philip, Sanjay Saran, Manish Gutch, Mohd Sayed Razi, Puspalata Agroiya, Keshavkumar Gupta
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 19, Iss 2, Pp 221-227 (2015)
Congenital hypothyroidism (CH) is the one of the most common preventable cause of mental retardation. In the majority of patients, CH is caused by an abnormal development of the thyroid gland (thyroid dysgenesis) that is a sporadic disorder and accou
Externí odkaz:
https://doaj.org/article/ffc77e54a47142dbab99fe408ec0c331
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 5, Iss 2, Pp 460-462 (2016)
Resistance to thyroid hormone syndrome (RTH) is a rare disorder and is usually inherited as dominantly negative autosomal trait. RTH is caused by mutations in the thyroid hormone receptor beta. Patients with RTH usually do not have signs and symptoms
Externí odkaz:
https://doaj.org/article/e207ae15785b410da8030a614a33debb
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 5, Pp 794-798 (2013)
Noonan Syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical face dysmorphology, and congenital heart defects. NS is a clinical diagnosis. Establishing the diagnosis can be very difficult, especially in adulthood. Th
Externí odkaz:
https://doaj.org/article/f0ff6f712ab649c28715492c49ef9bce
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 18, Iss 1, Pp 113-115 (2014)
Hashimoto′s encephalopathy (HE) is a rare steroid-responsive encephalopathy syndrome, which can have highly variable neuropsychiatric manifestations and can go unrecognized for a long time. HE is a diagnosis of exclusion and should be kept in mind
Externí odkaz:
https://doaj.org/article/eb51294ac81046f9a4e6bede0c0fd894
Autor:
Rajeev Philip, Sanjay Saran, Manish Gutch, Pushpaltha Agroyia, Rajiv Tyagi, Keshavkumar Gupta
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 157-159 (2013)
Pulse methylprednisolone therapy is the recommended therapy for moderate to severe and active ophthalmopathy, but high dose pulse methylprednisolone therapy is marred by the chances of fulminant hepatic failure and the high cost of therapy. Dexametha
Externí odkaz:
https://doaj.org/article/3f8cd6d67ec7452cbbced562cab93889
Autor:
Sanjay Saran, Rajeev Philip, Manish Gutch, Rajeev Tyagi, Puspalata Agroiya, Keshav Kumar Gupta
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 355-357 (2013)
Total 33 obese patients were studied to determine correlation in between liver fat content with dyslipidemia and insulin resistance. Liver and spleen attenuation measurements were taken with three regions of interests (ROIs) from the liver and two RO
Externí odkaz:
https://doaj.org/article/517c71e503564ae6befb82b74f7b4e9d
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 181-183 (2013)
Thyroid hormone mediates growth and development of the skeleton through its direct effects and through its permissive effects on growth hormone. The effect of hypothyroidism on bone is well described in congenital hypothyroidism, but the impact of th
Externí odkaz:
https://doaj.org/article/33e36ca1589f4956bf95a0b3f235713a
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 283-285 (2013)
Mauriac syndrome is a rare syndrome associated with type 1 diabetes (T1DM) in children presenting with growth retardation, hepatomegaly, and cushingoid features. Recently, there has been re-emergence of this syndrome, especially with the use of premi
Externí odkaz:
https://doaj.org/article/1ff84d482c01447ab39b660555b2b7a9