Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1989 1
1990 3
1991 4
1992 8
1993 8
1994 2
1995 2
1996 1
1997 5
1998 1
1999 1
2000 2
2001 1
2002 1
2003 1
2004 4
2005 2
2006 4
2007 3
2008 3
2009 1
2010 6
2011 5
2012 1
2013 2
2014 2
2015 2
2016 2
2017 2
2021 2
2022 1
Text availability
Article attribute
Article type
Publication date

Search Results

75 results
Results by year
Filters applied: . Clear all
Page 1
Multicolor karyotyping in acute myeloid leukemia.
Tchinda J, Volpert S, McNeil N, Neumann T, Kennerknecht I, Ried T, Büchner T, Serve H, Berdel WE, Horst J, Hilgenfeld E. Tchinda J, et al. Among authors: kennerknecht i. Leuk Lymphoma. 2003 Nov;44(11):1843-53. doi: 10.1080/10428190310001603605. Leuk Lymphoma. 2003. PMID: 14738135 Review.
DIDMOAD (Wolfram) syndrome.
Kellner M, Strian F, Fassbender K, Kennerknecht I, Klein R. Kellner M, et al. Among authors: kennerknecht i. Br J Psychiatry. 1994 Jan;164(1):132. doi: 10.1192/bjp.164.1.132a. Br J Psychiatry. 1994. PMID: 8137102 No abstract available.
Gaze behaviour in hereditary prosopagnosia.
Schwarzer G, Huber S, Grüter M, Grüter T, Gross C, Hipfel M, Kennerknecht I. Schwarzer G, et al. Among authors: kennerknecht i. Psychol Res. 2007 Sep;71(5):583-90. doi: 10.1007/s00426-006-0068-0. Epub 2006 Jun 10. Psychol Res. 2007. PMID: 16767465
Author's response.
Kennerknecht I I. Kennerknecht I I. Prenat Diagn. 1999 Sep;19(9):892. doi: 10.1002/(sici)1097-0223(199909)19:9<892::aid-pd643>3.0.co;2-1. Prenat Diagn. 1999. PMID: 10521855 No abstract available.
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta.
Lindert U, Cabral WA, Ausavarat S, Tongkobpetch S, Ludin K, Barnes AM, Yeetong P, Weis M, Krabichler B, Srichomthong C, Makareeva EN, Janecke AR, Leikin S, Röthlisberger B, Rohrbach M, Kennerknecht I, Eyre DR, Suphapeetiporn K, Giunta C, Marini JC, Shotelersuk V. Lindert U, et al. Among authors: kennerknecht i. Nat Commun. 2016 Jul 6;7:11920. doi: 10.1038/ncomms11920. Nat Commun. 2016. PMID: 27380894 Free PMC article.
Hereditary prosopagnosia: the first case series.
Grueter M, Grueter T, Bell V, Horst J, Laskowski W, Sperling K, Halligan PW, Ellis HD, Kennerknecht I. Grueter M, et al. Among authors: kennerknecht i. Cortex. 2007 Aug;43(6):734-49. doi: 10.1016/s0010-9452(08)70502-1. Cortex. 2007. PMID: 17710825
75 results