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126 novel mutations in Italian patients with neurofibromatosis type 1.
Bianchessi D, Morosini S, Saletti V, Ibba MC, Natacci F, Esposito S, Cesaretti C, Riva D, Finocchiaro G, Eoli M. Bianchessi D, et al. Among authors: esposito s. Mol Genet Genomic Med. 2015 Jul 7;3(6):513-25. doi: 10.1002/mgg3.161. eCollection 2015 Nov. Mol Genet Genomic Med. 2015. PMID: 26740943 Free PMC article.
Neurological pictures in paediatric Chiari I malformation.
Saletti V, Esposito S, Frittoli M, Valentini LG, Chiapparini L, Bulgheroni S, Riva D. Saletti V, et al. Among authors: esposito s. Neurol Sci. 2011 Dec;32 Suppl 3:S295-8. doi: 10.1007/s10072-011-0744-8. Neurol Sci. 2011. PMID: 21983864
Executive functions and cerebellar development in children.
Riva D, Cazzaniga F, Esposito S, Bulgheroni S. Riva D, et al. Among authors: esposito s. Appl Neuropsychol Child. 2013;2(2):97-103. doi: 10.1080/21622965.2013.791092. Epub 2013 Jun 9. Appl Neuropsychol Child. 2013. PMID: 23745837 Review.
Vasculogenic and Angiogenic Pathways in Moyamoya Disease.
Bedini G, Blecharz KG, Nava S, Vajkoczy P, Alessandri G, Ranieri M, Acerbi F, Ferroli P, Riva D, Esposito S, Pantaleoni C, Nardocci N, Zibordi F, Ciceri E, Parati EA, Bersano A. Bedini G, et al. Among authors: esposito s. Curr Med Chem. 2016;23(4):315-45. doi: 10.2174/092986732304160204181543. Curr Med Chem. 2016. PMID: 26861126 Review.
Legius Syndrome: two novel mutations in the SPRED1 gene.
Bianchi M, Saletti V, Micheli R, Esposito S, Molinaro A, Gagliardi S, Orcesi S, Cereda C. Bianchi M, et al. Among authors: esposito s. Hum Genome Var. 2015 Dec 3;2:15051. doi: 10.1038/hgv.2015.51. eCollection 2015. Hum Genome Var. 2015. PMID: 27081556 Free PMC article.
1,906 results