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Results by year

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

Year Number of Results
1920 1
1932 1
1941 1
1951 1
1954 7
1955 6
1956 1
1957 3
1958 7
1959 6
1960 3
1961 4
1962 4
1963 4
1965 1
1969 1
1970 1
1971 2
1975 2
1980 1
1981 1
1983 1
1986 2
1987 1
1988 3
1992 1
1993 1
1994 2
1995 2
1997 1
1998 4
1999 3
2000 6
2001 8
2002 5
2003 6
2004 1
2005 8
2006 14
2007 7
2008 8
2009 6
2010 1
2011 3
2012 1
2013 5
2014 2
2015 2
2016 2
2017 1
2018 1
2019 8
2020 5
2021 1
2022 2
2023 3
2024 0

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Similar articles for PMID: 16033916

173 results

Results by year

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Page 1
Congenital hyperinsulinism and mosaic abnormalities of the ploidy.
Giurgea I, Sanlaville D, Fournet JC, Sempoux C, Bellanné-Chantelot C, Touati G, Hubert L, Groos MS, Brunelle F, Rahier J, Henquin JC, Dunne MJ, Jaubert F, Robert JJ, Nihoul-Fékété C, Vekemans M, Junien C, de Lonlay P. Giurgea I, et al. J Med Genet. 2006 Mar;43(3):248-54. doi: 10.1136/jmg.2005.034116. Epub 2005 Jul 20. J Med Genet. 2006. PMID: 16033916 Free PMC article.
Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism.
Damaj L, le Lorch M, Verkarre V, Werl C, Hubert L, Nihoul-Fékété C, Aigrain Y, de Keyzer Y, Romana SP, Bellanne-Chantelot C, de Lonlay P, Jaubert F. Damaj L, et al. J Clin Endocrinol Metab. 2008 Dec;93(12):4941-7. doi: 10.1210/jc.2008-0673. Epub 2008 Sep 16. J Clin Endocrinol Metab. 2008. PMID: 18796520
Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.
Hussain K, Cosgrove KE, Shepherd RM, Luharia A, Smith VV, Kassem S, Gregory JW, Sivaprasadarao A, Christesen HT, Jacobsen BB, Brusgaard K, Glaser B, Maher EA, Lindley KJ, Hindmarsh P, Dattani M, Dunne MJ. Hussain K, et al. J Clin Endocrinol Metab. 2005 Jul;90(7):4376-82. doi: 10.1210/jc.2005-0158. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811927
Tissue variations of mosaic genome-wide paternal uniparental disomy and phenotype of multi-syndromal congenital hyperinsulinism.
Christesen HT, Christensen LG, Löfgren ÅM, Brøndum-Nielsen K, Svensson J, Brusgaard K, Samuelsson S, Elfving M, Jonson T, Grønskov K, Rasmussen L, Backman T, Hansen LK, Larsen AR, Petersen H, Detlefsen S. Christesen HT, et al. Eur J Med Genet. 2020 Jan;63(1):103632. doi: 10.1016/j.ejmg.2019.02.004. Epub 2019 Feb 21. Eur J Med Genet. 2020. PMID: 30797057 Free article.
173 results