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Pervasive supply of therapeutic lysosomal enzymes in the CNS of normal and Krabbe-affected non-human primates by intracerebral lentiviral gene therapy.
EMBO Mol Med. 2016 May 2;8(5):489-510. doi: 10.15252/emmm.201505850. Print 2016 May.
EMBO Mol Med. 2016.
PMID: 27025653
Free PMC article.
Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).
Godi M, Mellone S, Tiradani L, Marabese R, Bardelli C, Salerno M, Prodam F, Bellone S, Petri A, Momigliano-Richiardi P, Bona G, Giordano M.
Godi M, et al. Among authors: tiradani l.
J Clin Endocrinol Metab. 2012 Sep;97(9):E1791-7. doi: 10.1210/jc.2012-1527. Epub 2012 Jun 28.
J Clin Endocrinol Metab. 2012.
PMID: 22745233
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A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency.
Carlomagno Y, Salerno M, Vivenza D, Capalbo D, Godi M, Mellone S, Tiradani L, Corneli G, Momigliano-Richiardi P, Bona G, Giordano M.
Carlomagno Y, et al. Among authors: tiradani l.
J Endocrinol Invest. 2009 Sep;32(8):653-8. doi: 10.1007/BF03345736. Epub 2009 May 12.
J Endocrinol Invest. 2009.
PMID: 19498317
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A functional common polymorphism in the vitamin D-responsive element of the GH1 promoter contributes to isolated growth hormone deficiency.
Giordano M, Godi M, Mellone S, Petri A, Vivenza D, Tiradani L, Carlomagno Y, Ferrante D, Arrigo T, Corneli G, Bellone S, Giacopelli F, Santoro C, Bona G, Momigliano-Richiardi P.
Giordano M, et al. Among authors: tiradani l.
J Clin Endocrinol Metab. 2008 Mar;93(3):1005-12. doi: 10.1210/jc.2007-1918. Epub 2007 Dec 26.
J Clin Endocrinol Metab. 2008.
PMID: 18160466
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