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The challenge of hypophosphatasia diagnosis in adults: results from the HPP International Working Group Literature Surveillance.
Brandi ML, Khan AA, Rush ET, Ali DS, Al-Alwani H, Almonaei K, Alsarraf F, Bacrot S, Dahir KM, Dandurand K, Deal C, Ferrari SL, Giusti F, Guyatt G, Hatcher E, Ing SW, Javaid MK, Khan S, Kocijan R, Lewiecki EM, Linglart A, M'Hiri I, Marini F, Nunes ME, Rockman-Greenberg C, Seefried L, Simmons JH, Starling SR, Ward LM, Yao L, Brignardello-Petersen R, Roux C. Brandi ML, et al. Among authors: giusti f. Osteoporos Int. 2024 Mar;35(3):439-449. doi: 10.1007/s00198-023-06859-8. Epub 2023 Nov 20. Osteoporos Int. 2024. PMID: 37982856 Review.
Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast-ovarian cancer syndromes: a case report.
Papi L, Palli D, Masi L, Putignano AL, Congregati C, Zanna I, Marini F, Giusti F, Luzi E, Tonelli F, Genuardi M, Brandi ML, Falchetti A. Papi L, et al. Among authors: giusti f. Cancer Genet Cytogenet. 2009 Nov;195(1):75-9. doi: 10.1016/j.cancergencyto.2009.06.019. Cancer Genet Cytogenet. 2009. PMID: 19837273
Thyroid cancer: current molecular perspectives.
Giusti F, Falchetti A, Franceschelli F, Marini F, Tanini A, Brandi ML. Giusti F, et al. J Oncol. 2010;2010:351679. doi: 10.1155/2010/351679. Epub 2010 Mar 29. J Oncol. 2010. PMID: 20369062 Free PMC article.
Hereditary hyperparathyroidism syndromes.
Giusti F, Cavalli L, Cavalli T, Brandi ML. Giusti F, et al. J Clin Densitom. 2013 Jan-Mar;16(1):69-74. doi: 10.1016/j.jocd.2012.11.003. J Clin Densitom. 2013. PMID: 23374744 Review.
327 results