Results 211 to 220 of about 49,296 (268)
Acromegaly in an elderly male with hepatic malignancy: a case report of a diagnostic dilemma. [PDF]
Ann Med Surg (Lond)Sah RK, Devkota D, Sah CK, Pathak A.
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Acromegaly: pathogenesis, diagnosis, and management.
The Lancet Diabetes and Endocrinology, 2022Growth hormone-secreting pituitary adenomas that cause acromegaly arise as monoclonal expansions of differentiated somatotroph cells and are usually sporadic. They are almost invariably benign, yet they can be locally invasive and show progressive growth
M. Fleseriu +4 more
semanticscholar +1 more source
New England Journal of Medicine, 1990
Subcellular mechanisms support the notion of an intrinsic pituitary defect in acromegaly, with elevated growth hormone (GH) and insulin-like growth factor-1 (IGF-1) levels that affect the cardiovascular and respiratory system, as well as neoplastic cell proliferative activity.
Shlomo Melmed
exaly +4 more sources
Subcellular mechanisms support the notion of an intrinsic pituitary defect in acromegaly, with elevated growth hormone (GH) and insulin-like growth factor-1 (IGF-1) levels that affect the cardiovascular and respiratory system, as well as neoplastic cell proliferative activity.
Shlomo Melmed
exaly +4 more sources
Clinical Endocrinology, 1987
SUMMARYA personal series of 256 cases of acromegaly/gigantism seen over a 20‐year period from 1963 is described. The insidious nature of the condition resulted in delay in diagnosis which was often made by a doctor when seeing the patient for an unrelated problem.
+7 more sources
SUMMARYA personal series of 256 cases of acromegaly/gigantism seen over a 20‐year period from 1963 is described. The insidious nature of the condition resulted in delay in diagnosis which was often made by a doctor when seeing the patient for an unrelated problem.
+7 more sources