Similar articles for PMID: 17586837

Year	Number of Results
2003	1
2006	4
2007	8
2008	11
2009	12
2010	16
2011	5
2012	8
2013	7
2014	4
2015	10
2016	7
2017	6
2018	3
2019	6
2020	2
2021	3
2022	5
2024	0

1

SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome.

Zenker M, Horn D, Wieczorek D, Allanson J, Pauli S, van der Burgt I, Doerr HG, Gaspar H, Hofbeck M, Gillessen-Kaesbach G, Koch A, Meinecke P, Mundlos S, Nowka A, Rauch A, Reif S, von Schnakenburg C, Seidel H, Wehner LE, Zweier C, Bauhuber S, Matejas V, Kratz CP, Thomas C, Kutsche K. Zenker M, et al. J Med Genet. 2007 Oct;44(10):651-6. doi: 10.1136/jmg.2007.051276. Epub 2007 Jun 23. J Med Genet. 2007. PMID: 17586837 Free PMC article.

2

Management of nutritional and gastrointestinal issues in RASopathies: A narrative review.

Onesimo R, Giorgio V, Viscogliosi G, Sforza E, Kuczynska E, Margiotta G, Iademarco M, Proli F, Rigante D, Zampino G, Leoni C. Onesimo R, et al. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):478-493. doi: 10.1002/ajmg.c.32019. Epub 2022 Dec 14. Am J Med Genet C Semin Med Genet. 2022. PMID: 36515923 Review.

3

Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: A multifaceted disease with immunodeficiency and short stature.

Szczawińska-Popłonyk A, Popłonyk N, Niedziela M, Sowińska-Seidler A, Sztromwasser P, Jamsheer A, Obara-Moszyńska M. Szczawińska-Popłonyk A, et al. Front Pediatr. 2022 Oct 14;10:990111. doi: 10.3389/fped.2022.990111. eCollection 2022. Front Pediatr. 2022. PMID: 36313893 Free PMC article.

4

Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene.

Mercadante F, Piro E, Busè M, Salzano E, Ferrara A, Serra G, Passarello C, Corsello G, Piccione M. Mercadante F, et al. Ital J Pediatr. 2022 Aug 19;48(1):152. doi: 10.1186/s13052-022-01340-4. Ital J Pediatr. 2022. PMID: 35986401 Free PMC article.

5

Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients.

Papadopoulos G, Papadopoulou A, Kosma K, Papadimitriou A, Papaevangelou V, Kanaka-Gantenbein C, Bountouvi E, Kitsiou-Tzeli S. Papadopoulos G, et al. Eur J Pediatr. 2022 Oct;181(10):3691-3700. doi: 10.1007/s00431-022-04574-w. Epub 2022 Jul 29. Eur J Pediatr. 2022. PMID: 35904599

6

Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene.

Serra G, Felice S, Antona V, Di Pace MR, Giuffrè M, Piro E, Corsello G. Serra G, et al. Ital J Pediatr. 2022 May 4;48(1):65. doi: 10.1186/s13052-022-01241-6. Ital J Pediatr. 2022. PMID: 35509048 Free PMC article.

7

In-Silico and In-Vitro Analysis of Human SOS1 Protein Causing Noonan Syndrome - A Novel Approach to Explore the Molecular Pathways.

Sigamani V, Rajasingh S, Gurusamy N, Panda A, Rajasingh J. Sigamani V, et al. Curr Genomics. 2021 Dec 31;22(7):526-540. doi: 10.2174/1389202922666211130144221. Curr Genomics. 2021. PMID: 35386434 Free PMC article.

8

Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G.

Gurusamy N, Rajasingh S, Sigamani V, Rajasingh R, Isai DG, Czirok A, Bittel D, Rajasingh J. Gurusamy N, et al. Exp Cell Res. 2021 Mar 1;400(1):112508. doi: 10.1016/j.yexcr.2021.112508. Epub 2021 Feb 4. Exp Cell Res. 2021. PMID: 33549576 Free PMC article.

9

Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications.

Lissewski C, Chune V, Pantaleoni F, De Luca A, Capri Y, Brinkmann J, Lepri F, Daniele P, Leenders E, Mazzanti L, Scarano E, Radio FC, Kutsche K, Kuechler A, Gérard M, Ranguin K, Legendre M, Vial Y, van der Burgt I, Rinne T, Andreucci E, Mastromoro G, Digilio MC, Cave H, Tartaglia M, Zenker M. Lissewski C, et al. Eur J Hum Genet. 2021 Jan;29(1):51-60. doi: 10.1038/s41431-020-00708-6. Epub 2020 Aug 12. Eur J Hum Genet. 2021. PMID: 32788663 Free PMC article.

10

Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?

Ferrari L, Mangano E, Bonati MT, Monterosso I, Capitanio D, Chiappori F, Brambilla I, Gelfi C, Battaglia C, Bordoni R, Riva P. Ferrari L, et al. Eur J Hum Genet. 2020 Oct;28(10):1432-1445. doi: 10.1038/s41431-020-0658-0. Epub 2020 Jun 8. Eur J Hum Genet. 2020. PMID: 32514133 Free PMC article.

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