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Inhibition of IGF-I and B-FGF Stimulated Growth of Human Retinal Endothelial Cells by the Somatostatin Analogue, Octreotide: A Potential Treatment for Ocular NeovascularizationGrant, Maria B., Caballero, Sergio, Millard, William J. 20 October 1993 (has links)
No description available.
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AkromegaliePlöckinger, Ursula 10 April 2001 (has links)
Die Akromegalie - Folge eines Wachstumshormon (STH) sezernierenden Hypophysentumors - ist eine seltene Erkrankung. Bei früher Diagnose ist die Akromegalie gut behandelbar. Unbehandelt - oder zu spät behandelt - führt sie zu hoher Co-Morbidität und verkürzt das Leben. Endokrinologische Therapieziele wurden kürzlich definiert: Heilung bei STH / Acromegaly, caused by a growth hormone (GH)-secreting pituitary adenoma, is a rare disease. If diagnosed early therapeutic results are good. However, untreated or treated belatedly, acromegaly is associated with a high co-morbidity and reduced life-expectancy. The therapeutic goals have recently been defined as follows: complete remission or cure as GH
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