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

Year Number of Results
1995 1
1996 2
1997 1
1998 1
2000 1
2002 2
2003 2
2004 4
2005 6
2006 6
2007 3
2008 10
2009 10
2010 5
2011 4
2012 4
2013 2
2014 11
2015 11
2016 7
2017 4
2018 6
2019 5
2020 2
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Similar Articles for PMID: 32188669

98 results
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Page 1
Images of the month 2: A leopard never changes its spots.
Denny JW, Krishna S, Valiallah N, Fogo A, Natkunarajah J. Denny JW, et al. Clin Med (Lond). 2020 Mar;20(2):231-232. doi: 10.7861/clinmed.2019-0489. Clin Med (Lond). 2020. PMID: 32188669 Free PMC article. No abstract available.
Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene.
Digilio MC, Conti E, Sarkozy A, Mingarelli R, Dottorini T, Marino B, Pizzuti A, Dallapiccola B. Digilio MC, et al. Am J Hum Genet. 2002 Aug;71(2):389-94. doi: 10.1086/341528. Epub 2002 Jun 7. Am J Hum Genet. 2002. PMID: 12058348 Free PMC article.
PTPN11 mutations in LEOPARD syndrome.
Legius E, Schrander-Stumpel C, Schollen E, Pulles-Heintzberger C, Gewillig M, Fryns JP. Legius E, et al. J Med Genet. 2002 Aug;39(8):571-4. doi: 10.1136/jmg.39.8.571. J Med Genet. 2002. PMID: 12161596 Free PMC article.
A novel PTPN11 gene mutation bridges Noonan syndrome, multiple lentigines/LEOPARD syndrome and Noonan-like/multiple giant cell lesion syndrome.
Sarkozy A, Obregon MG, Conti E, Esposito G, Mingarelli R, Pizzuti A, Dallapiccola B. Sarkozy A, et al. Eur J Hum Genet. 2004 Dec;12(12):1069-72. doi: 10.1038/sj.ejhg.5201290. Eur J Hum Genet. 2004. PMID: 15470362 Free article.
LEOPARD syndrome: a variant of Noonan syndrome strongly associated with hypertrophic cardiomyopathy.
Carcavilla A, Santomé JL, Pinto I, Sánchez-Pozo J, Guillén-Navarro E, Martín-Frías M, Lapunzina P, Ezquieta B. Carcavilla A, et al. Rev Esp Cardiol (Engl Ed). 2013 May;66(5):350-6. doi: 10.1016/j.rec.2012.09.015. Epub 2013 Jan 11. Rev Esp Cardiol (Engl Ed). 2013. PMID: 24775816
LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD.
Kim J, Kim MR, Kim HJ, Lee KA, Lee MG. Kim J, et al. Ann Dermatol. 2011 May;23(2):232-5. doi: 10.5021/ad.2011.23.2.232. Epub 2011 May 27. Ann Dermatol. 2011. PMID: 21747628 Free PMC article.
A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype.
Edwards JJ, Martinelli S, Pannone L, Lo IF, Shi L, Edelmann L, Tartaglia M, Luk HM, Gelb BD. Edwards JJ, et al. Am J Med Genet A. 2014 Sep;164A(9):2351-5. doi: 10.1002/ajmg.a.36620. Epub 2014 May 28. Am J Med Genet A. 2014. PMID: 24891296 Free PMC article.
Cochlear implantation and clinical features in patients with Noonan syndrome and Noonan syndrome with multiple lentigines caused by a mutation in PTPN11.
van Nierop JWI, van Trier DC, van der Burgt I, Draaisma JMT, Mylanus EAM, Snik AF, Admiraal RJC, Kunst HPM. van Nierop JWI, et al. Int J Pediatr Otorhinolaryngol. 2017 Jun;97:228-234. doi: 10.1016/j.ijporl.2017.04.024. Epub 2017 Apr 17. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28483241
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