Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Azra, Niaz"'
Autor:
Shahnawaz Imam, Rodis D. Paparodis, Shafiya Imtiaz Rafiqi, Sophia Ali, Azra Niaz, Abed Kanzy, Yara E. Tovar, Mohammed A. Madkhali, Ahmed Elsherif, Feras Khogeer, Zeeshan A. Zahid, Haider Sarwar, Tamanna Karim, Nancy Salim, Juan C. Jaume
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
BackgroundThyroid nodules are an extremely common entity, and surgery is considered the ultimate diagnostic strategy in those with unclear malignant potential. Unfortunately, strategies aiming to predict the risk of malignancy have inadequate specifi
Externí odkaz:
https://doaj.org/article/9376399c3a5045148cd2934e3e64353d
Publikováno v:
Journal of the Endocrine Society
Introduction There has been a recent increase in the incidence of adrenal incidentaloma (AI), defined as an adrenal mass that’s unintentionally discovered on imaging obtained for an indication other than suspected adrenal pathology, mainly because
Metabolic Improvements After Gastric Sleeve Surgery in a Patient With Familial Partial Lipodystrophy
Autor:
Azra Niaz, Ali Sophia
Publikováno v:
Journal of the Endocrine Society
Familial Partial Lipodystrophy (FPLD) is a rare genetic disorder characterized by loss of subcutaneous adipose tissue mainly from peripheral areas but preservation, or increase, of fat in the face, neck, and trunk. This abnormal fat redistribution le
Autor:
Farzane Saeidifard, Asadullah Mahmood, Sean McConachie, Naba Saeed, Roheila Seyedtabaei, Rajiv John, Ali B. Saad, Azra Niaz
Publikováno v:
American Journal of Gastroenterology. 114:S692-S692
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 66(11)
To determine the incidence, aetiology and epidemiology of hospitalized patients with hyponatraemia.Subjects were identified through hospital information system for two consecutive low sodium values (130 mEq/L) and charts were reviewed retrospectively
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 66(2)
Idiopathic Retroperitoneal fibrosis is a rare clinical condition recently identified as an autoimmune process related to Immunoglobulin G4 (IgG4) deposition. Herein we report a case of a 46 year old male presenting with 4 months history of backache,