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

Year Number of Results
1947 1
1995 3
1996 2
1997 5
1998 3
1999 6
2000 5
2001 6
2002 8
2003 8
2004 6
2005 5
2006 8
2007 6
2009 5
2010 6
2011 7
2012 4
2013 6
2014 4
2015 2
2016 2
2017 5
2018 5
2019 4
2020 4
2021 4
2022 1
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Similar articles for PMID: 20511138

123 results
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Page 1
Hereditary hyperferritinaemia/ cataract syndrome.
Cazzola M. Cazzola M. Best Pract Res Clin Haematol. 2002 Jun;15(2):385-98. doi: 10.1016/s1521-6926(02)90204-5. Best Pract Res Clin Haematol. 2002. PMID: 12401313 Review.
Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE.
Papanikolaou G, Chandrinou H, Bouzas E, Contopoulos-Ioannidis D, Kalotychou V, Prentzas K, Lilakos K, Asproudis I, Palaiologou D, Premetis E, Papassotiriou I, Sakellaropoulos N. Papanikolaou G, et al. Blood Cells Mol Dis. 2006 Jan-Feb;36(1):33-40. doi: 10.1016/j.bcmd.2005.10.003. Epub 2006 Jan 5. Blood Cells Mol Dis. 2006. PMID: 16406710
123 results