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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 1
2010 3
2011 4
2012 2
2013 3
2014 4
2015 5
2016 3
2017 4
2018 5
2019 3
2020 6
2021 0
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35 results
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Page 1
Obsessive Compulsive Symptoms and Psychopathological Profile in Children and Adolescents with KBG syndrome.
Alfieri P, Demaria F, Licchelli S, Santonastaso O, Caciolo C, Digilio MC, Sinibaldi L, Leoni C, Gnazzo M, Tartaglia M, Pasqualetti P, Vicari S. Alfieri P, et al. Brain Sci. 2019 Nov 7;9(11):313. doi: 10.3390/brainsci9110313. Brain Sci. 2019. PMID: 31703437 Free PMC article.
TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics.
Sferra A, Petrini S, Bellacchio E, Nicita F, Scibelli F, Dentici ML, Alfieri P, Cestra G, Bertini ES, Zanni G. Sferra A, et al. Among authors: alfieri p. Int J Mol Sci. 2020 Feb 18;21(4):1385. doi: 10.3390/ijms21041385. Int J Mol Sci. 2020. PMID: 32085672 Free PMC article.
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling.
Dentici ML, Bergonzini P, Scibelli F, Caciolo C, De Rose P, Cumbo F, Alesi V, Capolino R, Zanni G, Sinibaldi L, Novelli A, Tartaglia M, Digilio MC, Dallapiccola B, Vicari S, Alfieri P. Dentici ML, et al. Among authors: alfieri p. Brain Sci. 2020 Nov 11;10(11):839. doi: 10.3390/brainsci10110839. Brain Sci. 2020. PMID: 33187326 Free PMC article.
Defining language disorders in children and adolescents with Noonan Syndrome.
Lazzaro G, Caciolo C, Menghini D, Cumbo F, Digilio MC, Capolino R, Zampino G, Tartaglia M, Vicari S, Alfieri P. Lazzaro G, et al. Among authors: alfieri p. Mol Genet Genomic Med. 2020 Apr;8(4):e1069. doi: 10.1002/mgg3.1069. Epub 2020 Feb 14. Mol Genet Genomic Med. 2020. PMID: 32059087 Free PMC article.
Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia.
Nicita F, Nardella M, Bellacchio E, Alfieri P, Terrone G, Piccini G, Graziola F, Pignata C, Capuano A, Bertini E, Zanni G. Nicita F, et al. Among authors: alfieri p. Clin Genet. 2019 Aug;96(2):169-175. doi: 10.1111/cge.13562. Epub 2019 Jun 5. Clin Genet. 2019. PMID: 31066025
Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation.
Stregapede F, Travaglini L, Rebelo AP, Cintra VP, Bellacchio E, Bosco L, Alfieri P, Pro S, Zuchner S, Bertini E, Nicita F. Stregapede F, et al. Among authors: alfieri p. Clin Genet. 2020 Mar;97(3):521-526. doi: 10.1111/cge.13668. Epub 2019 Dec 5. Clin Genet. 2020. PMID: 31705535
Neurobehavioral features in individuals with Kabuki syndrome.
Caciolo C, Alfieri P, Piccini G, Digilio MC, Lepri FR, Tartaglia M, Menghini D, Vicari S. Caciolo C, et al. Among authors: alfieri p. Mol Genet Genomic Med. 2018 May;6(3):322-331. doi: 10.1002/mgg3.348. Epub 2018 Mar 13. Mol Genet Genomic Med. 2018. PMID: 29536651 Free PMC article.
Psychopathological features in Noonan syndrome.
Perrino F, Licchelli S, Serra G, Piccini G, Caciolo C, Pasqualetti P, Cirillo F, Leoni C, Digilio MC, Zampino G, Tartaglia M, Alfieri P, Vicari S. Perrino F, et al. Among authors: alfieri p. Eur J Paediatr Neurol. 2018 Jan;22(1):170-177. doi: 10.1016/j.ejpn.2017.09.009. Epub 2017 Sep 28. Eur J Paediatr Neurol. 2018. PMID: 29037749
Comparison of Adaptive Functioning in Children with Williams Beuren Syndrome and Autism Spectrum Disorder: A Cross-Syndrome Study.
Alfieri P, Scibelli F, Digilio MC, Novello RL, Caciolo C, Valeri G, Vicari S. Alfieri P, et al. Autism Res. 2020 Dec 11. doi: 10.1002/aur.2455. Online ahead of print. Autism Res. 2020. PMID: 33314766
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases.
Alfieri P, Scibelli F, Sinibaldi L, Valeri G, Caciolo C, Novello RL, Novelli A, Digilio MC, Tartaglia M, Vicari S. Alfieri P, et al. Genes Brain Behav. 2020 Sep;19(7):e12687. doi: 10.1111/gbb.12687. Epub 2020 Aug 26. Genes Brain Behav. 2020. PMID: 32658356
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