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

Year Number of Results
1988 1
1989 2
1990 1
1998 3
1999 3
2000 1
2001 2
2002 2
2003 3
2004 2
2005 2
2006 3
2007 2
2008 5
2009 1
2010 2
2011 3
2012 5
2013 11
2014 12
2015 7
2016 6
2017 3
2018 8
2019 7
2020 11
2021 3
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Similar articles for PMID: 33632934

97 results
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Page 1
PIGA Mutations Can Mimic Neonatal Hemochromatosis.
Flores-Torres J, Carver JD, Sanchez-Valle A. Flores-Torres J, et al. Pediatrics. 2021 Mar;147(3):e20200918. doi: 10.1542/peds.2020-0918. Pediatrics. 2021. PMID: 33632934
The genotypic and phenotypic spectrum of PIGA deficiency.
Tarailo-Graovac M, Sinclair G, Stockler-Ipsiroglu S, Van Allen M, Rozmus J, Shyr C, Biancheri R, Oh T, Sayson B, Lafek M, Ross CJ, Robinson WP, Wasserman WW, Rossi A, van Karnebeek CD. Tarailo-Graovac M, et al. Orphanet J Rare Dis. 2015 Feb 27;10:23. doi: 10.1186/s13023-015-0243-8. Orphanet J Rare Dis. 2015. PMID: 25885527 Free PMC article.
Expanding the spectrum of phenotypes associated with germline PIGA mutations: a child with developmental delay, accelerated linear growth, facial dysmorphisms, elevated alkaline phosphatase, and progressive CNS abnormalities.
van der Crabben SN, Harakalova M, Brilstra EH, van Berkestijn FM, Hofstede FC, van Vught AJ, Cuppen E, Kloosterman W, Ploos van Amstel HK, van Haaften G, van Haelst MM. van der Crabben SN, et al. Am J Med Genet A. 2014 Jan;164A(1):29-35. doi: 10.1002/ajmg.a.36184. Epub 2013 Nov 20. Am J Med Genet A. 2014. PMID: 24259184 Review.
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