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Handbook of Clinical Neurology|September 22, 2020
Neurogenesis, neuronal migration, and axon guidanceAndrea Accogli, Nassima Addour-Boudrahem, Myriam Srour
Cerebellum (London, England)|February 3, 2021
Diagnostic Approach to Cerebellar HypoplasiaAndrea Accogli, Nassima Addour-Boudrahem, Myriam Srour
Molecular Cytogenetics|August 1, 2014
Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24.1q24.3 deletionElisa Tassano, Andrea Accogli, Serena Panigada, et al.
Immunotherapy|December 18, 2013
Serum-specific IgE and allergen immunotherapy in allergic childrenMariangela Tosca, Michela Silvestri, Michela Sivestri, et al.
Developmental Medicine and Child Neurology|October 16, 2018
Developmental outcomes in children with congenital cerebellar malformationsElana F Pinchefsky, Andrea Accogli, Michael I Shevell, et al.
Pediatric Neurology|December 25, 2018
Diagnostic Yield of Intellectual Disability Gene PanelsHeather Pekeles, Andrea Accogli, Nassima Boudrahem-Addour, et al.
European Journal of Medical Genetics|December 15, 2015
Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traitsElisa Tassano, Andrea Accogli, Marco Pavanello, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 7, 2021
A rare triad of morning glory disc anomaly, moyamoya vasculopathy, and transsphenoidal cephalocele: pathophysiological considerations and surgical managementMarco Pavanello, Pietro Fiaschi, Andrea Accogli, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 7, 2019
Chiari malformation type I: what information from the genetics?Valeria Capra, Michele Iacomino, Andrea Accogli, et al.
Birth Defects Research|May 3, 2017
A novel Xp22.13 microdeletion in Nance-Horan syndromeAndrea Accogli, Monica Traverso, Francesca Madia, et al.
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