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Items: 1 to 20 of 42

1.

Is my patient ready for a safe transfer to a lower-intensity care setting? Nursing complexity as an independent predictor of adverse events risk after ICU discharge.

Sanson G, Marino C, Valenti A, Lucangelo U, Berlot G.

Heart Lung. 2020 Feb 14. pii: S0147-9563(20)30015-7. doi: 10.1016/j.hrtlng.2020.02.003. [Epub ahead of print]

PMID:
32067723
2.

Paternal-but Not Maternal-Autistic Traits Predict Frontal EEG Alpha Asymmetry in Infants with Later Symptoms of Autism.

Riva V, Marino C, Piazza C, Riboldi EM, Mornati G, Molteni M, Cantiani C.

Brain Sci. 2019 Nov 26;9(12). pii: E342. doi: 10.3390/brainsci9120342.

3.

Postnatal maternal symptoms of depression and child emotion dysregulation: The mediation role of infant EEG alpha asymmetry.

Marino C, Riva V, Mornati G, Piazza C, Del Giudice R, Dionne G, Molteni M, Cantiani C.

Infant Behav Dev. 2019 Nov;57:101321. doi: 10.1016/j.infbeh.2019.04.003. Epub 2019 May 21.

PMID:
31125855
4.

Clinical utility of the CBCL Dysregulation Profile in children with disruptive behavior.

Aitken M, Battaglia M, Marino C, Mahendran N, Andrade BF.

J Affect Disord. 2019 Jun 15;253:87-95. doi: 10.1016/j.jad.2019.04.034. Epub 2019 Apr 9.

PMID:
31029857
5.

Reduced left-lateralized pattern of event-related EEG oscillations in infants at familial risk for language and learning impairment.

Cantiani C, Ortiz-Mantilla S, Riva V, Piazza C, Bettoni R, Musacchia G, Molteni M, Marino C, Benasich AA.

Neuroimage Clin. 2019;22:101778. doi: 10.1016/j.nicl.2019.101778. Epub 2019 Mar 12.

6.

Distinct ERP profiles for auditory processing in infants at-risk for autism and language impairment.

Riva V, Cantiani C, Mornati G, Gallo M, Villa L, Mani E, Saviozzi I, Marino C, Molteni M.

Sci Rep. 2018 Jan 15;8(1):715. doi: 10.1038/s41598-017-19009-y.

7.

The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects.

Trezzi V, Forni D, Giorda R, Villa M, Molteni M, Marino C, Mascheretti S.

J Hum Genet. 2017 Nov;62(11):949-955. doi: 10.1038/jhg.2017.80. Epub 2017 Aug 3.

PMID:
29066855
8.

Effects on the incidence of cardiovascular events of the addition of pioglitazone versus sulfonylureas in patients with type 2 diabetes inadequately controlled with metformin (TOSCA.IT): a randomised, multicentre trial.

Vaccaro O, Masulli M, Nicolucci A, Bonora E, Del Prato S, Maggioni AP, Rivellese AA, Squatrito S, Giorda CB, Sesti G, Mocarelli P, Lucisano G, Sacco M, Signorini S, Cappellini F, Perriello G, Babini AC, Lapolla A, Gregori G, Giordano C, Corsi L, Buzzetti R, Clemente G, Di Cianni G, Iannarelli R, Cordera R, La Macchia O, Zamboni C, Scaranna C, Boemi M, Iovine C, Lauro D, Leotta S, Dall'Aglio E, Cannarsa E, Tonutti L, Pugliese G, Bossi AC, Anichini R, Dotta F, Di Benedetto A, Citro G, Antenucci D, Ricci L, Giorgino F, Santini C, Gnasso A, De Cosmo S, Zavaroni D, Vedovato M, Consoli A, Calabrese M, di Bartolo P, Fornengo P, Riccardi G; Thiazolidinediones Or Sulfonylureas Cardiovascular Accidents Intervention Trial (TOSCA.IT) study group; Italian Diabetes Society.

Lancet Diabetes Endocrinol. 2017 Nov;5(11):887-897. doi: 10.1016/S2213-8587(17)30317-0. Epub 2017 Sep 13. Erratum in: Lancet Diabetes Endocrinol. 2017 Nov;5(11):e7.

PMID:
28917544
9.

ERP responses to lexical-semantic processing in typically developing toddlers, in adults, and in toddlers at risk for language and learning impairment.

Cantiani C, Riva V, Piazza C, Melesi G, Mornati G, Bettoni R, Marino C, Molteni M.

Neuropsychologia. 2017 Aug;103:115-130. doi: 10.1016/j.neuropsychologia.2017.06.031. Epub 2017 Jun 30.

PMID:
28669897
10.

From CNTNAP2 to Early Expressive Language in Infancy: The Mediation Role of Rapid Auditory Processing.

Riva V, Cantiani C, Benasich AA, Molteni M, Piazza C, Giorda R, Dionne G, Marino C.

Cereb Cortex. 2018 Jun 1;28(6):2100-2108. doi: 10.1093/cercor/bhx115.

PMID:
28498932
11.

A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples.

Mozzi A, Riva V, Forni D, Sironi M, Marino C, Molteni M, Riva S, Guerini FR, Clerici M, Cagliani R, Mascheretti S.

Am J Med Genet B Neuropsychiatr Genet. 2017 Jul;174(5):578-586. doi: 10.1002/ajmg.b.32546. Epub 2017 Apr 24.

PMID:
28436202
12.

Working memory mediates the effects of gestational age at birth on expressive language development in children.

Riva V, Cantiani C, Dionne G, Marini A, Mascheretti S, Molteni M, Marino C.

Neuropsychology. 2017 Jul;31(5):475-485. doi: 10.1037/neu0000376. Epub 2017 Apr 6.

PMID:
28383969
13.

Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.

Mascheretti S, Trezzi V, Giorda R, Boivin M, Plourde V, Vitaro F, Brendgen M, Dionne G, Marino C.

J Child Psychol Psychiatry. 2017 Jan;58(1):75-82. doi: 10.1111/jcpp.12612. Epub 2016 Aug 8.

PMID:
27501527
14.

Auditory discrimination predicts linguistic outcome in Italian infants with and without familial risk for language learning impairment.

Cantiani C, Riva V, Piazza C, Bettoni R, Molteni M, Choudhury N, Marino C, Benasich AA.

Dev Cogn Neurosci. 2016 Aug;20:23-34. doi: 10.1016/j.dcn.2016.03.002. Epub 2016 Mar 24.

15.

Strong motion deficits in dyslexia associated with DCDC2 gene alteration.

Cicchini GM, Marino C, Mascheretti S, Perani D, Morrone MC.

J Neurosci. 2015 May 27;35(21):8059-64. doi: 10.1523/JNEUROSCI.5077-14.2015.

16.

Phenotypic and genetic associations between reading comprehension, decoding skills, and ADHD dimensions: evidence from two population-based studies.

Plourde V, Boivin M, Forget-Dubois N, Brendgen M, Vitaro F, Marino C, Tremblay RT, Dionne G.

J Child Psychol Psychiatry. 2015 Oct;56(10):1074-82. doi: 10.1111/jcpp.12394. Epub 2015 Feb 12.

17.

GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia.

Mascheretti S, Facoetti A, Giorda R, Beri S, Riva V, Trezzi V, Cellino MR, Marino C.

Psychiatr Genet. 2015 Feb;25(1):9-20. doi: 10.1097/YPG.0000000000000068.

PMID:
25426763
18.

GRIN2B predicts attention problems among disadvantaged children.

Riva V, Battaglia M, Nobile M, Cattaneo F, Lazazzera C, Mascheretti S, Giorda R, Mérette C, Émond C, Maziade M, Marino C.

Eur Child Adolesc Psychiatry. 2015 Jul;24(7):827-36. doi: 10.1007/s00787-014-0627-7. Epub 2014 Oct 16.

PMID:
25316095
19.

The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability.

Gori S, Mascheretti S, Giora E, Ronconi L, Ruffino M, Quadrelli E, Facoetti A, Marino C.

Cereb Cortex. 2015 Jun;25(6):1685-95. doi: 10.1093/cercor/bhu234. Epub 2014 Sep 30.

PMID:
25270309
20.

The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.

Riva V, Marino C, Giorda R, Molteni M, Nobile M.

Eur Child Adolesc Psychiatry. 2015 Mar;24(3):309-18. doi: 10.1007/s00787-014-0580-5. Epub 2014 Jul 11.

PMID:
25012462

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