Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Reena Bharwaj"'
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 3, Pp 514-518 (2013)
Multiple endocrine neoplasia-1 (MEN1) is an autosomal dominant syndrome with classic triad of parathyroid hyperplasia, pancreatic neuroendocrine tumors, and pituitary adenomas. Other recognized manifestations include carcinoid, cutaneous or adrenocor
Externí odkaz:
https://doaj.org/article/45e637d25caf4d45ae6ee4bbb0b991ed
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 4, Pp 759-762 (2013)
A 19-year-old girl presented with classical features of Cushing′s syndrome. Endocrinal evaluation was consistent with pituitary source of ACTH; but imaging showed normal pituitary. Bilateral inferior petrosal sinus sampling confirmed the diagnosis.
Externí odkaz:
https://doaj.org/article/60a587c203f44dd58b082053b0b20fb5
Autor:
Abhay Gundgurthi, Sandeep Kharb, M K Garg, K S Brar, Reena Bharwaj, Srishti Gupta, H C Pathak
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 5, Pp 846-849 (2012)
We report a case of 41-year-old lady who presented with chronic headache of 6-month duration and a sellar mass with a suprasellar extension on imaging, which was interpreted as pituitary macroadenoma. She had normal pituitary function and visual peri
Externí odkaz:
https://doaj.org/article/41e3fe7690544ddfbafc0b70a72e474b
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 6, Pp 1114-1116 (2013)
Nelson′s syndrome refers to a clinical spectrum arising from progressive enlargement of pituitary adenoma and elevated adrenocorticotrophic hormone after total bilateral adrenalectomy for Cushing′s disease comprising of hyperpigmentation, visual
Externí odkaz:
https://doaj.org/article/bc3d2a0b65604706abdc3e89bb7c12d6
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 4, Pp 759-762 (2013)
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism
A 19-year-old girl presented with classical features of Cushing's syndrome. Endocrinal evaluation was consistent with pituitary source of ACTH; but imaging showed normal pituitary. Bilateral inferior petrosal sinus sampling confirmed the diagnosis. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52bb0e4a6cb273d2fac4e62874c392fc
http://www.ijem.in/article.asp?issn=2230-8210
http://www.ijem.in/article.asp?issn=2230-8210
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 3, Pp 514-518 (2013)
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism
Multiple endocrine neoplasia-1 (MEN1) is an autosomal dominant syndrome with classic triad of parathyroid hyperplasia, pancreatic neuroendocrine tumors, and pituitary adenomas. Other recognized manifestations include carcinoid, cutaneous or adrenocor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3777f886e029229f37016443c723d6c
http://www.ijem.in/article.asp?issn=2230-8210
http://www.ijem.in/article.asp?issn=2230-8210
Autor:
Srishti Gupta, Sandeep Kharb, Reena Bharwaj, HC Pathak, MK Garg, K. S. Brar, Abhay Gundgurthi
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 16, Iss 5, Pp 846-849 (2012)
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism
We report a case of 41-year-old lady who presented with chronic headache of 6-month duration and a sellar mass with a suprasellar extension on imaging, which was interpreted as pituitary macroadenoma. She had normal pituitary function and visual peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d5bd0ebc288e1c72010e4a3c65bbd48
http://www.ijem.in/article.asp?issn=2230-8210
http://www.ijem.in/article.asp?issn=2230-8210
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 6, Pp 1114-1116 (2013)
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism
Nelson's syndrome refers to a clinical spectrum arising from progressive enlargement of pituitary adenoma and elevated adrenocorticotrophic hormone after total bilateral adrenalectomy for Cushing's disease comprising of hyperpigmentation, visual fiel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44feaa910abdf848b87ed46aec91ccb5
https://doi.org/10.4103/2230-8210.122643
https://doi.org/10.4103/2230-8210.122643