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Page 1
Gene Therapy with Voretigene Neparvovec Improves Vision and Partially Restores Electrophysiological Function in Pre-School Children with Leber Congenital Amaurosis.
Gerhardt MJ, Priglinger CS, Rudolph G, Hufendiek K, Framme C, Jägle H, Salchow DJ, Anschütz A, Michalakis S, Priglinger SG. Gerhardt MJ, et al. Biomedicines. 2022 Dec 30;11(1):103. doi: 10.3390/biomedicines11010103. Biomedicines. 2022. PMID: 36672611 Free PMC article.
Leber congenital amaurosis caused by mutations in the RPE65 gene belongs to the most severe early-onset hereditary childhood retinopathies naturally progressing to legal blindness. ...
Leber congenital amaurosis caused by mutations in the RPE65 gene belongs to the most severe early-onset hereditary childhood retinopa …
Analysis of three genes in Leber congenital amaurosis in Indonesian patients.
Sitorus RS, Lorenz B, Preising MN. Sitorus RS, et al. Vision Res. 2003 Dec;43(28):3087-93. doi: 10.1016/j.visres.2003.08.008. Vision Res. 2003. PMID: 14611946 Free article.
PURPOSE: To assess the frequency, the pattern of disease causing mutations, and phenotypic variations in patients with Leber congenital amaurosis (LCA) from Indonesia. PATIENTS AND METHODS: Twenty-one unrelated index cases with a clinical diagnosis of LCA were screened for …
PURPOSE: To assess the frequency, the pattern of disease causing mutations, and phenotypic variations in patients with Leber congenit …
Sitagliptin plus granulocyte colony-stimulating factor in patients suffering from acute myocardial infarction: A double-blind, randomized placebo-controlled trial of efficacy and safety (SITAGRAMI trial).
Brenner C, Adrion C, Grabmaier U, Theisen D, von Ziegler F, Leber A, Becker A, Sohn HY, Hoffmann E, Mansmann U, Steinbeck G, Franz WM, Theiss HD. Brenner C, et al. Int J Cardiol. 2016 Feb 15;205:23-30. doi: 10.1016/j.ijcard.2015.11.180. Epub 2015 Nov 30. Int J Cardiol. 2016. PMID: 26709136 Clinical Trial.
Longitudinal and cross-sectional study of patients with early-onset severe retinal dystrophy associated with RPE65 mutations.
Paunescu K, Wabbels B, Preising MN, Lorenz B. Paunescu K, et al. Graefes Arch Clin Exp Ophthalmol. 2005 May;243(5):417-26. doi: 10.1007/s00417-004-1020-x. Epub 2004 Nov 24. Graefes Arch Clin Exp Ophthalmol. 2005. PMID: 15565294
CONCLUSION: In childhood, patients with RPE65 mutations have better visual functions than typically seen in Leber congenital amaurosis. The phenotype shows a common progressive pattern with intrafamilial and interfamilial variation. ...
CONCLUSION: In childhood, patients with RPE65 mutations have better visual functions than typically seen in Leber congenital amaurosi …
Discovery of aminofurazan-azabenzimidazoles as inhibitors of Rho-kinase with high kinase selectivity and antihypertensive activity.
Stavenger RA, Cui H, Dowdell SE, Franz RG, Gaitanopoulos DE, Goodman KB, Hilfiker MA, Ivy RL, Leber JD, Marino JP Jr, Oh HJ, Viet AQ, Xu W, Ye G, Zhang D, Zhao Y, Jolivette LJ, Head MS, Semus SF, Elkins PA, Kirkpatrick RB, Dul E, Khandekar SS, Yi T, Jung DK, Wright LL, Smith GK, Behm DJ, Doe CP, Bentley R, Chen ZX, Hu E, Lee D. Stavenger RA, et al. J Med Chem. 2007 Jan 11;50(1):2-5. doi: 10.1021/jm060873p. J Med Chem. 2007. PMID: 17201404
Detection of significant coronary artery stenosis with 64-slice computed tomography in heart transplant recipients: a comparative study with conventional coronary angiography.
von Ziegler F, Leber AW, Becker A, Kaczmarek I, Schönermarck U, Raps C, Tittus J, Uberfuhr P, Becker CR, Reiser M, Steinbeck G, Knez A. von Ziegler F, et al. Int J Cardiovasc Imaging. 2009 Jan;25(1):91-100. doi: 10.1007/s10554-008-9343-z. Epub 2008 Jul 19. Int J Cardiovasc Imaging. 2009. PMID: 18642098
[Bacterial infections of the liver in the elderly].
Diridl G, Lenhart V, Pichler H. Diridl G, et al. Z Arztl Fortbild (Jena). 1992 Oct 26;86(20):1007-12. Z Arztl Fortbild (Jena). 1992. PMID: 1441637 German. No abstract available.