Pseudo-TORCH syndrome or Baraitser-Reardon syndrome : diagnostic criteriaVIVARELLI, Rossella; GROSSO, Salvatore; CIONI, Maddalena et al.Brain & development (Tokyo. 1979). 2001, Vol 23, Num 1, pp 18-23, issn 0387-7604Article

Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 geneSESTINI, Roberta; VIVARELLI, Rossella; BALESTRI, Paolo et al.Human genetics. 2000, Vol 107, Num 4, pp 366-371, issn 0340-6717Article

GM2 gangliosidosis variant B1: Neuroradiological findingsGROSSO, Salvatore; FARNETANI, Maria Angela; BERARDI, Rosario et al.Journal of neurology. 2003, Vol 250, Num 1, pp 17-21, issn 0340-5354, 5 p.Article

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationBACCI, Costanza; SESTINI, Roberta; PROVENZANO, Aldesia et al.Neurogenetics (Oxford. Print). 2010, Vol 11, Num 1, pp 73-80, issn 1364-6745, 8 p.Article

Craniofacial dyssynostosis: Case report and reviewGROSSO, Salvatore; VIVARELLI, Rossella; MURACA, Maria Carmela et al.American journal of medical genetics. 2004, Vol 129A, Num 3, pp 300-302, issn 0148-7299, 3 p.Article