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The case of the solitary sick kidney.
Stratta P, Canavese C, Monzani A, Corrado L, Giordano M. Stratta P, et al. Among authors: giordano m. Kidney Int. 2010 Feb;77(3):257-8; author reply 258. doi: 10.1038/ki.2009.450. Kidney Int. 2010. PMID: 20075957 Free article. No abstract available.
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
De Rienzo F, Mellone S, Bellone S, Babu D, Fusco I, Prodam F, Petri A, Muniswamy R, De Luca F, Salerno M, Momigliano-Richardi P, Bona G, Giordano M; Italian Study Group on Genetics of CPHD. De Rienzo F, et al. Among authors: giordano m. Clin Endocrinol (Oxf). 2015 Dec;83(6):849-60. doi: 10.1111/cen.12849. Epub 2015 Aug 6. Clin Endocrinol (Oxf). 2015. PMID: 26147833 Review.
A recurrent signal peptide mutation in the growth hormone releasing hormone receptor with defective translocation to the cell surface and isolated growth hormone deficiency.
Godi M, Mellone S, Petri A, Arrigo T, Bardelli C, Corrado L, Bellone S, Prodam F, Momigliano-Richiardi P, Bona G, Giordano M. Godi M, et al. Among authors: giordano m. J Clin Endocrinol Metab. 2009 Oct;94(10):3939-47. doi: 10.1210/jc.2009-0833. Epub 2009 Jul 21. J Clin Endocrinol Metab. 2009. PMID: 19622623
Role of CES1 and ABCB1 Genetic Polymorphisms on Functional Response to Dabigatran in Patients with Atrial Fibrillation.
Cumitini L, Renda G, Giordano M, Rolla R, Shail T, Sacchetti S, Iezzi L, Giacomini L, Zanotti V, Auciello R, Angilletta I, Foglietta M, Zucchelli M, Antonucci I, Stuppia L, Gallina S, Dianzani U, Patti G. Cumitini L, et al. Among authors: giordano m. J Clin Med. 2024 Apr 26;13(9):2545. doi: 10.3390/jcm13092545. J Clin Med. 2024. PMID: 38731074 Free PMC article.
1,636 results