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Journal Abstract Search
359 related items for PubMed ID: 12766032
1. Age-dependent iris abnormalities in collagen XVIII/endostatin deficient mice with similarities to human pigment dispersion syndrome. Marneros AG, Olsen BR. Invest Ophthalmol Vis Sci; 2003 Jun; 44(6):2367-72. PubMed ID: 12766032 [Abstract] [Full Text] [Related]
12. Localization of collagen XVIII and endostatin in the human eye. Ohlmann AV, Ohlmann A, Welge-Lüssen U, May CA. Curr Eye Res; 2005 Jan; 30(1):27-34. PubMed ID: 15875362 [Abstract] [Full Text] [Related]
14. A histopathologic study of iris changes in pseudoexfoliation syndrome. Asano N, Schlötzer-Schrehardt U, Naumann GO. Ophthalmology; 1995 Sep; 102(9):1279-90. PubMed ID: 9097764 [Abstract] [Full Text] [Related]
15. Localization of collagen XVIII and the endostatin portion of collagen XVIII in aged human control eyes and eyes with age-related macular degeneration. Bhutto IA, Kim SY, McLeod DS, Merges C, Fukai N, Olsen BR, Lutty GA. Invest Ophthalmol Vis Sci; 2004 May; 45(5):1544-52. PubMed ID: 15111613 [Abstract] [Full Text] [Related]
16. Endostatin overexpression specifically in the lens and skin leads to cataract and ultrastructural alterations in basement membranes. Elamaa H, Sormunen R, Rehn M, Soininen R, Pihlajaniemi T. Am J Pathol; 2005 Jan; 166(1):221-9. PubMed ID: 15632014 [Abstract] [Full Text] [Related]
17. Persistence of fetal vasculature in a patient with Knobloch syndrome: potential role for endostatin in fetal vascular remodeling of the eye. Duh EJ, Yao YG, Dagli M, Goldberg MF. Ophthalmology; 2004 Oct; 111(10):1885-8. PubMed ID: 15465551 [Abstract] [Full Text] [Related]
18. Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome. Suzuki OT, Sertié AL, Der Kaloustian VM, Kok F, Carpenter M, Murray J, Czeizel AE, Kliemann SE, Rosemberg S, Monteiro M, Olsen BR, Passos-Bueno MR. Am J Hum Genet; 2002 Dec; 71(6):1320-9. PubMed ID: 12415512 [Abstract] [Full Text] [Related]
19. The exfoliation syndrome. Sugar HS, Harding C, Barsky D. Ann Ophthalmol; 1976 Oct; 8(10):1165-81. PubMed ID: 984637 [Abstract] [Full Text] [Related]