Syndrome de Noonan (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Syndrome de Noonan" in French language version.

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3sciencedirect.com

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2nih.gov

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2thelancet.com

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2wiley.com

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1ahajournals.org

3,608^th place

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1sagepub.com

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1bmj.com

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1nature.com

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1springer.com

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ahajournals.org

Hanses U, Kleinsorge M, Roos L et al. Intronic CRISPR repair in a preclinical model of Noonan syndrome–associated cardiomyopathy, Circulation, 2020;142:1059–1076

bmj.com

adc.bmj.com

(en) Sharland M, Burch M, McKenna WM, Paton MA, « A clinical study of Noonan syndrome » Arch Dis Child. 1992;67:178-183.

nature.com

(en) Jongmans MC, van der Burgt I, Hoogerbrugge PM et al. « Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation » Eur J Hum Genet. 2011;19:870-874.

nih.gov

ncbi.nlm.nih.gov

(en) Curcić-Stojković O, Nikolić L, Obradović D, Krstić A, Radić A, « [Noonan's syndrome. (Male Turner's syndrome, Turner-like syndrome)] », Med Pregl, vol. 31(7–8),‎ 1978, p. 299–303 (PMID 692497)
(en) Marcus KA, Sweep CG, van der Burgt I, Noordam C, « Impaired Sertoli cell function in males diagnosed with Noonan syndrome » J Pediatr Endocrinol Metab. 2008;21:1079-1084.

sagepub.com

oto.sagepub.com

(en) Qiu WW, Yin SS, Stucker FJ, « Audiologic manifestations of Noonan syndrome » Otolaryngol Head Neck Surg. 1998;118:319-323.

sciencedirect.com

(en) Tartaglia M, Kalidas K, Shaw A et al. « PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity » Am J Hum Genet. 2002;70:1555-1563
Aoki Y, Niihori T, Banjo T et al. Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome, Am J Hum Genet, 2013; 93:173–180
(en) Marino B, Digilio MC, Toscano A, Giannotti A, Dallapiccola B, « Congenital heart diseases in children with Noonan syndrome: an expanded cardiac spectrum with high prevalence of atrioventricular canal » J Pediatr. 1999;135:703-706

springer.com

link.springer.com

(en) Takagi M, Miyashita Y, Koga M, Ebara S, Arita N, Kasayama S, « Estrogen deficiency is a potential cause for osteopenia in adult male patients with Noonan's syndrome » Calcif Tissue Int. 2000;66:200-203.

thelancet.com

(en) Roberts AE, Allanson JE, Tartaglia M, Gelb BD, « Noonan syndrome », Lancet 2013;381:333-342
(en) Sharland M, Patton MA, Talbot S, Chitolie A, Bevan DH, « Coagulation-factor deficiencies and abnormal bleeding in Noonan's syndrome » Lancet 1992;339:19-21

wiley.com

onlinelibrary.wiley.com

Gripp KW, Aldinger KA, Bennett JT et al. A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair, Am J Med. Genet A. 2016;170:2237–2247
(en) Lee DA, Portnoy S, Hill P, Gillberg C, Patton MA, « Psychological profile of children with Noonan syndrome » Dev Med Child Neurol. 2005;47:35-38.