Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 5
1973 1
1974 3
1975 1
1976 1
1983 3
1985 2
1986 1
1992 2
1993 1
1994 2
1996 3
1997 4
1998 6
1999 2
2000 3
2001 2
2002 4
2024 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

46 results

Results by year

Filters applied: . Clear all
Page 1
Ten novel mutations found in Aniridia.
Wolf MT, Lorenz B, Winterpacht A, Drechsler M, Schumacher V, Royer-Pokora B, Blankenagel A, Zabel B, Wildhardt G. Wolf MT, et al. Among authors: blankenagel a. Hum Mutat. 1998;12(5):304-13. doi: 10.1002/(SICI)1098-1004(1998)12:5<304::AID-HUMU3>3.0.CO;2-D. Hum Mutat. 1998. PMID: 9792406
[Reading aids for subjects with impaired vision].
Jaeger W, Blankenagel A, Hudelmeyer D, Will G. Jaeger W, et al. Among authors: blankenagel a. Dtsch Med Wochenschr. 1974 Nov 15;99(46):2365-8. doi: 10.1055/s-0028-1108132. Dtsch Med Wochenschr. 1974. PMID: 4609720 Review. German. No abstract available.
[Satisfaction with low vision aids].
Rohrschneider K, Kiel R, Pavlovska V, Blankenagel A. Rohrschneider K, et al. Among authors: blankenagel a. Klin Monbl Augenheilkd. 2002 Jul;219(7):507-11. doi: 10.1055/s-2002-33585. Klin Monbl Augenheilkd. 2002. PMID: 12195316 German.
The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.
Maugeri A, van Driel MA, van de Pol DJ, Klevering BJ, van Haren FJ, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Dahl N, Brunner HG, Deutman AF, Hoyng CB, Cremers FP. Maugeri A, et al. Among authors: blankenagel a. Am J Hum Genet. 1999 Apr;64(4):1024-35. doi: 10.1086/302323. Am J Hum Genet. 1999. PMID: 10090887 Free PMC article.
Television reading system.
Blankenagel A, Jaeger W. Blankenagel A, et al. Child Care Health Dev. 1975 Sep-Oct;1(5):369-72. doi: 10.1111/j.1365-2214.1975.tb00221.x. Child Care Health Dev. 1975. PMID: 131004
46 results