Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ritesh Kumar Agrawala"'
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 19, Iss 1, Pp 143-147 (2015)
Aims and objectives: To study the frequency of thyroid, adrenal and gonadal dysfunction in newly diagnosed HIV-infected patients and to correlate them at different levels of CD4 cell counts. Materials and Methods: Forty-three HIV-positive cases were
Externí odkaz:
https://doaj.org/article/65a9b12a75c94746b9e91546c2bfe590
Autor:
Ritesh Kumar Agrawala, Srikanta Kumar Sahoo, Arun Kumar Choudhury, Binoy Kumar Mohanty, Anoj Kumar Baliarsinha
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 254-256 (2013)
A 35-year-female presented with generalized weakness, weight loss, and progressive pigmentation was worked up for suspicion of Addisons disease. On examination hyper pigmentation was noted on both palmar and dorsal aspect of hands involving knuckles,
Externí odkaz:
https://doaj.org/article/4ed3d7e6cfec4a51871bb1cf39bbaf61
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 271-273 (2013)
The sex of an embryo is determined by genetic sex due to presence or absence of Y chromosome, but it may not be true in all. We hereby report an interesting case of a phenotypic male carrying a female karyotype (46 XX). A 26-year-old male presented w
Externí odkaz:
https://doaj.org/article/7d13f5f3be7c4b76a028d67248ef00df
Autor:
Dr. Ritesh Kumar Agrawala, Dr. SS Akbar, Dr. Kaushik Biswas, Dr. Nithin Reddy Modhugu, Dr. Umesh Kumar Garg, Dr. Sona Warrier, Dr. Ashish Prasad, Dr. Ashish Birla
Objective: To evaluate the opinions of Indian clinical experts and aid in clinical choices for the optimal use of vildagliptin-dapagliflozin fixed-dose combination (FDC) for treating type 2 diabetes (T2D) in Indian patients. Methods: The virtual roun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cf6661fcfcaa07a1102062e0f8146be
Autor:
Ritesh Kumar Agrawala, Suchita Agarwal, Arun Chudhury, Binoy Kumar Mohanty, Anoj Kumar Baliarsinha
Publikováno v:
Journal of Diabetes & Metabolism.
Objective: Metabolic parameters in polycystic ovary syndrome (PCOS) correlate to their phenotypic presentations and sources of hyperandrogenism. Till date no studies have evaluated the source of hyperandrogenism among phenotypic variants of PCOS. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2c37cfca391c55ff7e1b019dd51d1ea
https://doi.org/10.4172/2155-6156.1000747
https://doi.org/10.4172/2155-6156.1000747
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 28
Perrault syndrome is a rare genetically heterogeneous autosomal recessive group of disorders described in 1951 by Perrault as gonadal dysgenesis with deafness. Here we present a rare case of sporadic Perrault syndrome with short stature and growth ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db765b1d4e2203e021991121d8f01256
https://doi.org/10.1515/jpem-2014-0292
https://doi.org/10.1515/jpem-2014-0292
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 271-273 (2013)
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism
The sex of an embryo is determined by genetic sex due to presence or absence of Y chromosome, but it may not be true in all. We hereby report an interesting case of a phenotypic male carrying a female karyotype (46 XX). A 26-year-old male presented w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b6c640816b3db03d6f2fd1b087b83e
http://www.ijem.in/article.asp?issn=2230-8210
http://www.ijem.in/article.asp?issn=2230-8210
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 27
Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare autosomal recessive disorder characterized by a nearly complete absence of adipose tissue and generalized muscular appearance. This condition is associated with various dermatological and sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68442b1e70b7c6c11648adbf7eaafafd
https://doi.org/10.1515/jpem-2013-0399
https://doi.org/10.1515/jpem-2013-0399
Autor:
Arun Kumar Choudhury, S.K. Sahoo, Ritesh Kumar Agrawala, Anoj Kumar Baliarsinha, Binoy Kumar Mohanty
Publikováno v:
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 254-256 (2013)
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 7, Pp 254-256 (2013)
A 35-year-female presented with generalized weakness, weight loss, and progressive pigmentation was worked up for suspicion of Addisons disease. On examination hyper pigmentation was noted on both palmar and dorsal aspect of hands involving knuckles,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7958c45928479331b18bf0a87c7d21c
https://doi.org/10.4103/2230-8210.119591
https://doi.org/10.4103/2230-8210.119591