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Mara GIORDANO: List of publications

10 of the last most significative publications
  1. M. Giordano, M. Godi, M. Lessi, S. Mellone, R. Paracchini, F. Giacopelli, R. Ravazzolo, G. Bona, P. Momigliano-Richiardi. A variation in a Pit-1 site in the GH1 promoter induces a differential  transcriptional activity. Molecular and Cellular Endocrinology, 2006;249:51-7 
  2. M. Giordano, C. Marano, M. Mellai,  M. Giovanna Limongelli, E. Bolognesi, F. Clerget-Darpoux,   P. Momigliano-Richiardi,  L. Greco.   A family based study does not confirm the association of MYO9B with celiac disease in the Italian population. Genes and Immunity, 2006 ;7 :606-8.  
  3. D. Vivenza, L. Guazzarotti, M. Godi, D. Frasca, B. di Natale, G. Bona, P. Momigliano-Richiardi and M. Giordano.  A novel deletion in the GH1 gene including the IVS3 branch site responsible for   autosomic dominant isolated growth hormone deficiency (IGHD-II). J Clinical Endocrinology and Metabolism, 2006 91:980-6.  
  4. M Giordano, M  Godi , S Mellone , A Petri , D  Vivenza , L  Tiradani , Y  Carlomagno , D  Ferrante , T Arrigo G Corneli, S Bellone, F Giacopelli , C  Santoro , G Bona , P  Momigliano-Richiardi. A functional common polymorphism in the Vitamin D-Responsive Element of the GH1 promoter contributes to Isolated Growth Hormone Deficiency. J Clinical Endocrinology and Metabolism, 2008 93:  1005-1012  
  5. M. Godi, S. Mellone, A. Petri, T. Arrigo, C. Bardelli, L. Corrado, S. Bellone, F. Prodam, P. Momigliano-Richiardi, G. Bona and M. Giordano. A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency. J Clinical Endocrinology and Metabolism, 2009 94: 3939-47
  6. Carlomagno Y, Salerno M, Vivenza D,  Capalbo D,  Godi M., Mellone S., Tiradani L., Corneli G., Momigliano-Richiardi P., Bona G. and  Giordano M.  A novel recessive splicing mutation in the POU1F1 Gene causing Combined Pituitary Hormone Deficiency , Journal of Endocrinological Investigation,  2009     32:653-658
  7. D  Vivenza, M Godi, M F Faienza ,S  Mellone, S Moia, A Rapa, A Petri, S Bellone, S Riccomagno, L Cavallo, M Giordano and G Bona. A novel HESX1 splice mutation causes Isolated Growth Hormone Deficiency by interfering  with mRNA processing. 2011  164(5):705-13.  European Journal of Endocrinology,   2011 164: 705-13
  8. Godi M, Mellone S, Tiradani L, Marabese R, Bardelli C, Salerno M, Prodam F, Bellone S, Petri A, Momigliano-Richiardi P, Bona G and Giordano M. Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD). J Clin Endocrinol Metab.  2012  97:  1791-7  
  9. Musetti C, Quaglia M, Mellone S, Pagani A, Fusco I, Monzani A, Giordano M, Stratta P.  Chronic Renal Failure of onknown origin is Caused by HNF1B mutations in 9% of adult patients: a single center cohort analysis. Nephrology   doi: 10.1111/nep.12199. [Epub ahead of print] 2014
  10. D. Babu, S. Mellone, I.Fusco , A.Petri, G.E. Walker, S.Bellone, F.Prodam, P. Momigliano-Richiardi, G.Bona and M. Giordano.  Novel Mutations  in  the Growth Hormone Gene (GH1)  Uncover  Putative Splicing Regulatory Elements.  Endocrinology, 2014 in press
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