Scordo MR - Search Results

1

Neurodevelopmental Disorders and Adaptive Functions: A Study of Children With Autism Spectrum Disorders (ASD) and/or Attention Deficit and Hyperactivity Disorder (ADHD).

Scandurra V, Emberti Gialloreti L, Barbanera F, Scordo MR, Pierini A, Canitano R. Scandurra V, et al. Among authors: scordo mr. Front Psychiatry. 2019 Sep 4;10:673. doi: 10.3389/fpsyt.2019.00673. eCollection 2019. Front Psychiatry. 2019. PMID: 31551839 Free PMC article.

2

Phenotypic spectrum of GABRA1: From generalized epilepsies to severe epileptic encephalopathies.

Johannesen K, Marini C, Pfeffer S, Møller RS, Dorn T, Niturad CE, Gardella E, Weber Y, Søndergård M, Hjalgrim H, Nikanorova M, Becker F, Larsen LH, Dahl HA, Maier O, Mei D, Biskup S, Klein KM, Reif PS, Rosenow F, Elias AF, Hudson C, Helbig KL, Schubert-Bast S, Scordo MR, Craiu D, Djémié T, Hoffman-Zacharska D, Caglayan H, Helbig I, Serratosa J, Striano P, De Jonghe P, Weckhuysen S, Suls A, Muru K, Talvik I, Talvik T, Muhle H, Borggraefe I, Rost I, Guerrini R, Lerche H, Lemke JR, Rubboli G, Maljevic S. Johannesen K, et al. Among authors: scordo mr. Neurology. 2016 Sep 13;87(11):1140-51. doi: 10.1212/WNL.0000000000003087. Epub 2016 Aug 12. Neurology. 2016. PMID: 27521439

3

22q11 deletion syndrome and multiple complex developmental disorder: a case report.

Scandurra V, Scordo MR, Canitano R, de Bruin EI. Scandurra V, et al. Among authors: scordo mr. J Clin Med Res. 2013 Apr;5(2):135-9. doi: 10.4021/jocmr1222w. Epub 2013 Feb 25. J Clin Med Res. 2013. PMID: 23519073 Free PMC article.

4

372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.

Marseglia G, Scordo MR, Pescucci C, Nannetti G, Biagini E, Scandurra V, Gerundino F, Magi A, Benelli M, Torricelli F. Marseglia G, et al. Among authors: scordo mr. Eur J Med Genet. 2012 Mar;55(3):216-21. doi: 10.1016/j.ejmg.2012.01.005. Epub 2012 Jan 25. Eur J Med Genet. 2012. PMID: 22333924

5

Nicolaides-Baraitser syndrome: two new cases with autism spectrum disorder.

Gana S, Panizzon M, Fongaro D, Selicorni A, Memo L, Scandurra V, Vannucci C, Bigozzi M, Scordo MR. Gana S, et al. Among authors: scordo mr. Clin Dysmorphol. 2011 Jan;20(1):38-41. doi: 10.1097/MCD.0b013e32833edaa9. Clin Dysmorphol. 2011. PMID: 20802310

6

A shifting level model algorithm that identifies aberrations in array-CGH data.

Magi A, Benelli M, Marseglia G, Nannetti G, Scordo MR, Torricelli F. Magi A, et al. Among authors: scordo mr. Biostatistics. 2010 Apr;11(2):265-80. doi: 10.1093/biostatistics/kxp051. Epub 2009 Nov 30. Biostatistics. 2010. PMID: 19948744

7

Anderson-Fabry disease with cerebrovascular complications in two Italian families.

Borsini W, Giuliacci G, Torricelli F, Pelo E, Martinelli F, Scordo MR. Borsini W, et al. Among authors: scordo mr. Neurol Sci. 2002 Jun;23(2):49-53. doi: 10.1007/s100720200025. Neurol Sci. 2002. PMID: 12235491

8

Anderson-Fabry disease: molecular analysis and clinical manifestations in three Italian families.

Torricelli F, Martinelli F, Pelo E, Minuti B, Borsini W, Battini ML, Scordo MR, Sodi A, Salvadori M. Torricelli F, et al. Among authors: scordo mr. Contrib Nephrol. 2001;(136):216-22. doi: 10.1159/000060189. Contrib Nephrol. 2001. PMID: 11688383 No abstract available.

9

Use of primed in situ labeling (PRINS) for the detection of telomeric deletions associated with mental retardation.

Bonifacio S, Centrone C, Da Prato L, Scordo MR, Estienne M, Torricelli F. Bonifacio S, et al. Among authors: scordo mr. Cytogenet Cell Genet. 2001;93(1-2):16-8. doi: 10.1159/000056939. Cytogenet Cell Genet. 2001. PMID: 11474170

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