Zespół Noonan (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół Noonan" in Polish language version.

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7nih.gov

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2doi.org

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1endojournals.org

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doi.org

Soultanis KC, Payatakes AH, Chouliaras VT, Mandellos GC, Pyrovolou NE, Pliarchopoulou FM, Soucacos PN. Rare causes of scoliosis and spine deformity: experience and particular features. „Scoliosis”. 2. 15, 2007. DOI: 10.1186/1748-7161-2-15. PMID: 17956633.

dx.doi.org

Kelnar CJ. Growth hormone therapy for syndromic disorders. „Clin Endocrinol(Oxford)”. 59. 1, s. 12–21, 2003. PMID: 12807497.

endojournals.org

jcem.endojournals.org

Yoshida R, Hasegawa T, Hasegawa Y, Nagai T, Kinoshita E, Tanaka Y, Kanegane H, Ohyama K, Onishi T, Hanew K, Okuyama T, Horikawa R, Tanaka T, Ogata T. Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. „J Clin Endocrinol Metab”. 89. 7, s. 3359–3364, 2004. PMID: 15240615.

nih.gov

ncbi.nlm.nih.gov

Soultanis KC, Payatakes AH, Chouliaras VT, Mandellos GC, Pyrovolou NE, Pliarchopoulou FM, Soucacos PN. Rare causes of scoliosis and spine deformity: experience and particular features. „Scoliosis”. 2. 15, 2007. DOI: 10.1186/1748-7161-2-15. PMID: 17956633.
Nora JJ, Nora AH, Sinha AK, Spangler RD, Lubs HA. The Ullrich-Noonan syndrome (Turner phenotype). „Am J Dis Child”. 127. 1, s. 48–55, 1974. PMID: 4809794.
Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, Brunner HG, Bertola DR, Crosby A, Ion A, Kucherlapati RS, Jeffery S, Patton MA, Gelb BD. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. „Am J Hum Genet”. 70. 6, s. 1555–1563, 2002. PMID: 11992261.
Yoshida R, Hasegawa T, Hasegawa Y, Nagai T, Kinoshita E, Tanaka Y, Kanegane H, Ohyama K, Onishi T, Hanew K, Okuyama T, Horikawa R, Tanaka T, Ogata T. Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome. „J Clin Endocrinol Metab”. 89. 7, s. 3359–3364, 2004. PMID: 15240615.
Kelnar CJ. Growth hormone therapy for syndromic disorders. „Clin Endocrinol(Oxford)”. 59. 1, s. 12–21, 2003. PMID: 12807497.
Opitz JM, Pallister PD. Brief historical note: the concept of ‘gonadal dysgenesis.’. „Am J Med Genet”. 4, s. 333–343, 1979. PMID: 395846.
Cole RB. Noonan’s syndrome: a historical perspective. „Pediatrics”. 66 (3), s. 468–469, 1980. PMID: 6999448.