Riccomagno S - Search Results

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Isolated GHD: investigation and implication of JAK/STAT related genes before and after rhGH treatment.

Trovato L, Riccomagno S, Prodam F, Genoni G, Walker GE, Moia S, Bellone S, Bona G. Trovato L, et al. Among authors: riccomagno s. Pituitary. 2012 Dec;15(4):482-9. doi: 10.1007/s11102-011-0354-8. Pituitary. 2012. PMID: 22038029

Involvement of genes related to inflammation and cell cycle in idiopathic short stature.

Trovato L, Prodam F, Genoni G, De Rienzo F, Walker GE, Moia S, Riccomagno S, Bellone S, Bona G. Trovato L, et al. Among authors: riccomagno s. Pituitary. 2013 Mar;16(1):83-90. doi: 10.1007/s11102-012-0378-8. Pituitary. 2013. PMID: 22382915

A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing.

Vivenza D, Godi M, Faienza MF, Mellone S, Moia S, Rapa A, Petri A, Bellone S, Riccomagno S, Cavallo L, Giordano M, Bona G. Vivenza D, et al. Among authors: riccomagno s. Eur J Endocrinol. 2011 May;164(5):705-13. doi: 10.1530/EJE-11-0047. Epub 2011 Feb 16. Eur J Endocrinol. 2011. PMID: 21325470

Noonan-like syndrome with loose anagen hair associated with growth hormone insensitivity and atypical neurological manifestations.

Capalbo D, Melis D, De Martino L, Palamaro L, Riccomagno S, Bona G, Cordeddu V, Pignata C, Salerno M. Capalbo D, et al. Among authors: riccomagno s. Am J Med Genet A. 2012 Apr;158A(4):856-60. doi: 10.1002/ajmg.a.35234. Epub 2012 Mar 14. Am J Med Genet A. 2012. PMID: 22419608

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