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Fragile X syndrome: a review of clinical and molecular diagnoses.
Ciaccio C, Fontana L, Milani D, Tabano S, Miozzo M, Esposito S. Ciaccio C, et al. Among authors: milani d. Ital J Pediatr. 2017 Apr 19;43(1):39. doi: 10.1186/s13052-017-0355-y. Ital J Pediatr. 2017. PMID: 28420439 Free PMC article. Review.
Think about it: FMR1 gene mosaicism.
Bonarrigo FA, Russo S, Vizziello P, Menni F, Cogliati F, Giorgini V, Monti F, Milani D. Bonarrigo FA, et al. Among authors: milani d. J Child Neurol. 2014 Sep;29(9):NP74-7. doi: 10.1177/0883073813503187. Epub 2013 Sep 23. J Child Neurol. 2014. PMID: 24065579
Is it time to change the neurofibromatosis 1 diagnostic criteria?
Tadini G, Milani D, Menni F, Pezzani L, Sabatini C, Esposito S. Tadini G, et al. Among authors: milani d. Eur J Intern Med. 2014 Jul;25(6):506-10. doi: 10.1016/j.ejim.2014.04.004. Epub 2014 Apr 29. Eur J Intern Med. 2014. PMID: 24784952 Review.
Ehlers-Danlos syndrome versus cleidocranial dysplasia.
Bedeschi MF, Bonarrigo F, Manzoni F, Milani D, Piemontese MR, Guez S, Esposito S. Bedeschi MF, et al. Among authors: milani d. Ital J Pediatr. 2014 May 24;40:49. doi: 10.1186/1824-7288-40-49. Ital J Pediatr. 2014. PMID: 24887404 Free PMC article. No abstract available.
A multidisciplinary approach in neurofibromatosis 1.
Milani D, Pezzani L, Tadini G, Menni F, Esposito S. Milani D, et al. Lancet Neurol. 2015 Jan;14(1):29-30. doi: 10.1016/S1474-4422(14)70255-8. Lancet Neurol. 2015. PMID: 25496892 No abstract available.
345 results