Similar articles for PMID: 32188669

Year	Number of Results
1995	1
1997	1
2000	1
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2003	3
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2005	7
2006	8
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2010	5
2011	4
2012	4
2013	3
2014	8
2015	9
2016	5
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2018	3
2019	9
2020	4
2021	5
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2024	1

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.

2

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.

3

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.

4

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

5

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

6

[Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome].

Froster UG, Glander HJ, Heinritz W. Froster UG, et al. Hautarzt. 2003 Dec;54(12):1190-2. doi: 10.1007/s00105-003-0640-0. Hautarzt. 2003. PMID: 14634749 German.

7

Extensive abdominal lipomatosis in a patient with Noonan/LEOPARD syndrome (Noonan syndrome-Multiple Lentigines).

Piard J, Verloes A, Cavé H, Peuchmaur M, Bennaceur S, Leheup B. Piard J, et al. Am J Med Genet A. 2012 Jun;158A(6):1406-10. doi: 10.1002/ajmg.a.35329. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22528600

8

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

9

Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.

Kalidas K, Shaw AC, Crosby AH, Newbury-Ecob R, Greenhalgh L, Temple IK, Law C, Patel A, Patton MA, Jeffery S. Kalidas K, et al. J Hum Genet. 2005;50(1):21-25. doi: 10.1007/s10038-004-0212-x. Epub 2004 Dec 10. J Hum Genet. 2005. PMID: 15690106

10

PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype.

Bertola DR, Pereira AC, Albano LM, De Oliveira PS, Kim CA, Krieger JE. Bertola DR, et al. Genet Test. 2006 Fall;10(3):186-91. doi: 10.1089/gte.2006.10.186. Genet Test. 2006. PMID: 17020470

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