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Items: 42

1.

Risk of Developmental Coordination Disorder in Italian very preterm children at school age compared to general population controls.

Caravale B, Herich L, Zoia S, Capone L, Voller F, Carrozzi M, Chiandotto V, Balottin U, Lacchei M, Croci I, Cuttini M.

Eur J Paediatr Neurol. 2019 Mar;23(2):296-303. doi: 10.1016/j.ejpn.2019.01.002. Epub 2019 Jan 11.

PMID:
30711366
2.

The lost children: The underdiagnosis of dyslexia in Italy. A cross-sectional national study.

Barbiero C, Montico M, Lonciari I, Monasta L, Penge R, Vio C, Tressoldi PE, Carrozzi M, De Petris A, De Cagno AG, Crescenzi F, Tinarelli G, Leccese A, Pinton A, Belacchi C, Tucci R, Musinu M, Tossali ML, Antonucci AM, Perrone A, Lentini Graziano M, Ronfani L; of behalf of the EpiDIt (Epidemiology of Dyslexia in Italy) working group.

PLoS One. 2019 Jan 23;14(1):e0210448. doi: 10.1371/journal.pone.0210448. eCollection 2019.

3.

Characteristics of EEG power spectrum during sleep spindle events in ADHD children.

De Dea F, Zanus C, Carrozzi M, Stecca M, Accardo A.

Conf Proc IEEE Eng Med Biol Soc. 2018 Jul;2018:1456-1459. doi: 10.1109/EMBC.2018.8512486.

PMID:
30440667
4.

An evaluation of the Movement ABC-2 Test for use in Italy: A comparison of data from Italy and the UK.

Zoia S, Biancotto M, Guicciardi M, Lecis R, Lucidi F, Pelamatti GM, Carrozzi M, Skabar A, Sugden DA, Barnett AL, Henderson SE.

Res Dev Disabil. 2019 Jan;84:43-56. doi: 10.1016/j.ridd.2018.04.013. Epub 2018 Apr 30.

PMID:
29716782
5.

19p13 microduplications encompassing NFIX are responsible for intellectual disability, short stature and small head circumference.

Trimouille A, Houcinat N, Vuillaume ML, Fergelot P, Boucher C, Toutain J, Caignec CL, Vincent M, Nizon M, Andrieux J, Vanlerberghe C, Delobel B, Duban B, Mansour S, Baple E, McKeown C, Poke G, Robertshaw K, Fifield E, Fabretto A, Pecile V, Gasparini P, Carrozzi M, Lacombe D, Arveiler B, Rooryck C, Moutton S.

Eur J Hum Genet. 2018 Jan;26(1):85-93. doi: 10.1038/s41431-017-0037-7. Epub 2017 Nov 28.

6.

Risk Factors and Outcomes of Thalidomide-induced Peripheral Neuropathy in a Pediatric Inflammatory Bowel Disease Cohort.

Bramuzzo M, Stocco G, Montico M, Arrigo S, Calvi A, Lanteri P, Costa S, Pellegrino S, Magazzù G, Barp J, Ghione S, Lionetti P, Zuin G, Fontana M, Di Chio T, Maggiore G, Lazzerini M, Lucafò M, Udina C, Pellegrin MC, Chicco A, Carrozzi M, Decorti G, Ventura A, Martelossi S.

Inflamm Bowel Dis. 2017 Oct;23(10):1810-1816. doi: 10.1097/MIB.0000000000001195.

PMID:
28817461
7.

Atypical presentation of anti-N-methyl-D-aspartate receptor encephalitis: two case reports.

Maggio MC, Mastrangelo G, Skabar A, Ventura A, Carrozzi M, Santangelo G, Vanadia F, Corsello G, Cimaz R.

J Med Case Rep. 2017 Aug 16;11(1):225. doi: 10.1186/s13256-017-1388-y.

8.

Adolescent Admissions to Emergency Departments for Self-Injurious Thoughts and Behaviors.

Zanus C, Battistutta S, Aliverti R, Montico M, Cremaschi S, Ronfani L, Monasta L, Carrozzi M.

PLoS One. 2017 Jan 26;12(1):e0170979. doi: 10.1371/journal.pone.0170979. eCollection 2017.

9.

Early diagnosis and Early Start Denver Model intervention in autism spectrum disorders delivered in an Italian Public Health System service.

Devescovi R, Monasta L, Mancini A, Bin M, Vellante V, Carrozzi M, Colombi C.

Neuropsychiatr Dis Treat. 2016 Jun 14;12:1379-84. doi: 10.2147/NDT.S106850. eCollection 2016.

10.

Carbamazepine-induced thrombocytopenic purpura in a child: Insights from a genomic analysis.

Abate MV, Stocco G, Devescovi R, Carrozzi M, Pierobon C, Valencic E, Lucafò M, Di Silvestre A, D'Adamo P, Tommasini A, Decorti G, Ventura A.

Blood Cells Mol Dis. 2016 Jul;59:97-9. doi: 10.1016/j.bcmd.2016.05.001. Epub 2016 May 3. No abstract available.

PMID:
27282575
11.

Diagnostic criteria currently proposed for "ictal epileptic headache": Perspectives on strengths, weaknesses and pitfalls.

Parisi P, Verrotti A, Costa P, Striano P, Zanus C, Carrozzi M, Raucci U, Villa MP, Belcastro V.

Seizure. 2015 Sep;31:56-63. doi: 10.1016/j.seizure.2015.07.005. Epub 2015 Jul 17.

12.

A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation.

Barone R, Carrozzi M, Parini R, Battini R, Martinelli D, Elia M, Spada M, Lilliu F, Ciana G, Burlina A, Leuzzi V, Leoni M, Sturiale L, Matthijs G, Jaeken J, Di Rocco M, Garozzo D, Fiumara A.

J Neurol. 2015 Jan;262(1):154-64. doi: 10.1007/s00415-014-7549-7. Epub 2014 Oct 30.

PMID:
25355454
13.

Acute pseudotumoral hemicerebellitis in a child: a rare and distinct entity?

Alberini E, Vellante V, Zennaro F, Calligaris L, Barbi E, Carrozzi M, Devescovi R.

J Child Neurol. 2015 Mar;30(4):496-9. doi: 10.1177/0883073814545114. Epub 2014 Aug 19.

PMID:
25143480
14.

[Interrater reliability of the Bayley III test in the Italian Northern-Adriatic Cohort II].

Deroma L, Bin M, Tognin V, Rosolen V, Valent F, Barbone F, Carrozzi M.

Epidemiol Prev. 2013 Jul-Oct;37(4-5):297-302. Italian.

PMID:
24293495
15.

PMM2-CDG: phenotype and genotype in four affected family members.

Bortot B, Cosentini D, Faletra F, Biffi S, De Martino E, Carrozzi M, Severini GM.

Gene. 2013 Dec 1;531(2):506-9. doi: 10.1016/j.gene.2013.07.083. Epub 2013 Aug 26.

PMID:
23988505
16.

Associations of prenatal mercury exposure from maternal fish consumption and polyunsaturated fatty acids with child neurodevelopment: a prospective cohort study in Italy.

Valent F, Mariuz M, Bin M, Little D, Mazej D, Tognin V, Tratnik J, McAfee AJ, Mulhern MS, Parpinel M, Carrozzi M, Horvat M, Tamburlini G, Barbone F.

J Epidemiol. 2013 Sep 5;23(5):360-70. Epub 2013 Aug 10.

17.

The submerged dyslexia iceberg: how many school children are not diagnosed? Results from an Italian study.

Barbiero C, Lonciari I, Montico M, Monasta L, Penge R, Vio C, Tressoldi PE, Ferluga V, Bigoni A, Tullio A, Carrozzi M, Ronfani L; CENDi (National Committee on the Epidemiology of Dyslexia) working group; Epidemiology of Dyslexia of Friuli Venezia Giulia working group (FVGwg).

PLoS One. 2012;7(10):e48082. doi: 10.1371/journal.pone.0048082. Epub 2012 Oct 31.

18.

Stem cells in severe infantile spinal muscular atrophy (SMA1).

Carrozzi M, Amaddeo A, Biondi A, Zanus C, Monti F, Alessandro V.

Neuromuscul Disord. 2012 Nov;22(11):1032-4. doi: 10.1016/j.nmd.2012.09.005. Epub 2012 Oct 6. No abstract available.

PMID:
23046997
19.

Extra-large letter spacing improves reading in dyslexia.

Zorzi M, Barbiero C, Facoetti A, Lonciari I, Carrozzi M, Montico M, Bravar L, George F, Pech-Georgel C, Ziegler JC.

Proc Natl Acad Sci U S A. 2012 Jul 10;109(28):11455-9. doi: 10.1073/pnas.1205566109. Epub 2012 Jun 4.

20.

Involuntary movements after correction of vitamin B12 deficiency: a video-case report.

Zanus C, Alberini E, Costa P, Colonna F, Zennaro F, Carrozzi M.

Epileptic Disord. 2012 Jun;14(2):174-80. doi: 10.1684/epd.2012.0507.

21.

Does the 1.5 Mb microduplication in chromosome band Xp22.31 have a pathogenetic role? New contribution and a review of the literature.

Faletra F, D'Adamo AP, Santa Rocca M, Carrozzi M, Perrone MD, Pecile V, Gasparini P.

Am J Med Genet A. 2012 Feb;158A(2):461-4. doi: 10.1002/ajmg.a.34398. Epub 2011 Dec 2. No abstract available.

PMID:
22140086
22.

Quantification of heteroplasmic mitochondrial DNA mutations for DNA samples in the low picogram range by nested real-time ARMS-qPCR.

Biffi S, Bortot B, Carrozzi M, Severini GM.

Diagn Mol Pathol. 2011 Jun;20(2):117-22. doi: 10.1097/PDM.0b013e3181efe2c6.

PMID:
21532488
23.

Neuromotor deficits in developmental coordination disorder: evidence from a reach-to-grasp task.

Biancotto M, Skabar A, Bulgheroni M, Carrozzi M, Zoia S.

Res Dev Disabil. 2011 Jul-Aug;32(4):1293-300. doi: 10.1016/j.ridd.2011.02.007. Epub 2011 Mar 5.

PMID:
21377830
24.

A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature.

Faletra F, Devescovi R, Pecile V, Fabretto A, Carrozzi M, Gasparini P.

J Appl Genet. 2011 Feb;52(1):77-80. doi: 10.1007/s13353-010-0004-2. Epub 2010 Nov 3. No abstract available.

PMID:
21107783
25.

The Tolosa-Hunt syndrome in children: a case report.

Zanus C, Furlan C, Costa P, Cosentini D, Carrozzi M.

Cephalalgia. 2009 Nov;29(11):1232-7. doi: 10.1111/j.1468-2982.2009.01856.x. Epub 2009 Apr 9.

PMID:
19558537
26.

Two novel cosegregating mutations in tRNAMet and COX III, in a patient with exercise intolerance and autoimmune polyendocrinopathy.

Bortot B, Barbi E, Biffi S, Angelini C, Faleschini E, Severini GM, Carrozzi M.

Mitochondrion. 2009 Apr;9(2):123-9. doi: 10.1016/j.mito.2009.01.006. Epub 2009 Jan 21.

PMID:
19460300
27.

Trisomy 12p and monosomy 4p: phenotype-genotype correlation.

Benussi DG, Costa P, Zollino M, Murdolo M, Petix V, Carrozzi M, Pecile V.

Genet Test Mol Biomarkers. 2009 Apr;13(2):199-204.

PMID:
19378504
28.

1q44-qter trisomy: clinical report and review of the literature.

Lenzini E, Ballarati L, Drigo P, Carrozzi M, Gambel-Benussi D, Giardino D, Petix V, Rizzotto MR, Pecile V.

Genet Test Mol Biomarkers. 2009 Feb;13(1):79-86. doi: 10.1089/gtmb.2008.0075. Review.

PMID:
19309278
29.

Two novel POLG mutations causing hepatic mitochondrial DNA depletion with recurrent hypoketotic hypoglycaemia and fatal liver dysfunction.

Bortot B, Barbi E, Biffi S, Lunazzi G, Bussani R, Burlina A, Norbedo S, Ventura A, Carrozzi M, Severini GM.

Dig Liver Dis. 2009 Jul;41(7):494-9. doi: 10.1016/j.dld.2008.11.013. Epub 2009 Feb 4.

PMID:
19195941
30.

Carbamazepine hypersensitivity syndrome triggered by a human herpes virus reactivation in a genetically predisposed patient.

Calligaris L, Stocco G, De Iudicibus S, Marino S, Decorti G, Barbi E, Carrozzi M, Marchetti F, Bartoli F, Ventura A.

Int Arch Allergy Immunol. 2009;149(2):173-7. doi: 10.1159/000189202. Epub 2009 Jan 6.

PMID:
19127076
31.

Chronic tension-type headache in adolescents. Clinical and psychological characteristics analyzed through self- and parent-report questionnaires.

Battistutta S, Aliverti R, Montico M, Zin R, Carrozzi M.

J Pediatr Psychol. 2009 Aug;34(7):697-706. doi: 10.1093/jpepsy/jsn102. Epub 2008 Oct 16.

PMID:
18927182
32.

Carbohydrate-deficient transferrin (CDT) as a biochemical tool for the screening of congenital disorders of glycosylation (CDGs).

Biffi S, Tamaro G, Bortot B, Zamberlan S, Severini GM, Carrozzi M.

Clin Biochem. 2007 Dec;40(18):1431-4. Epub 2007 Sep 6.

PMID:
17920054
33.

Comorbidity of DCD and SLI: Significance of epileptiform activity during sleep.

Scabar A, Devescovi R, Blason L, Bravar L, Carrozzi M.

Child Care Health Dev. 2006 Nov;32(6):733-9.

PMID:
17018048
34.

A comparison of the reach-to-grasp movement between children and adults: a kinematic study.

Zoia S, Pezzetta E, Blason L, Scabar A, Carrozzi M, Bulgheroni M, Castiello U.

Dev Neuropsychol. 2006;30(2):719-38.

PMID:
16995833
35.
36.

Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report.

Demori E, Devescovi R, Benussi DG, Dolce S, Carrozzi M, Villa N, Miertus J, Amoroso A, Pecile V.

Am J Med Genet A. 2004 Oct 15;130A(3):288-94. Review.

PMID:
15378554
37.

Gaucher's disease with Parkinson's disease: clinical and pathological aspects.

Bembi B, Zambito Marsala S, Sidransky E, Ciana G, Carrozzi M, Zorzon M, Martini C, Gioulis M, Pittis MG, Capus L.

Neurology. 2003 Jul 8;61(1):99-101.

PMID:
12847165
38.

Carbohydrate-deficient glycoprotein syndromes: the Italian experience.

Di Rocco M, Barone R, Adami A, Burlina A, Carrozzi M, Dionisi-Vici C, Gatti R, Iannetti P, Parini R, Raucci U, Roccella M, Spada M, Fiumara A.

J Inherit Metab Dis. 2000 Jun;23(4):391-5. No abstract available.

PMID:
10896302
39.

Use of the fractal dimension for the analysis of electroencephalographic time series.

Accardo A, Affinito M, Carrozzi M, Bouquet F.

Biol Cybern. 1997 Nov;77(5):339-50.

PMID:
9418215
40.

Endozepine stupor in children.

Soriani S, Carrozzi M, De Carlo L, Plazzi G, Provini F, Rothstein JD, Tinuper P, Bouquet F, Lugaresi E, Montagna P.

Cephalalgia. 1997 Oct;17(6):658-61.

PMID:
9350386
41.

Enzyme replacement treatment in type 1 and type 3 Gaucher's disease.

Bembi B, Zanatta M, Carrozzi M, Baralle F, Gornati R, Berra B, Agosti E.

Lancet. 1994 Dec 17;344(8938):1679-82.

PMID:
7996964
42.

Mutagenicity test of extracts of airborne dust from the municipal incinerator of Trieste.

Pani B, Laureni U, Babudri N, Collareta A, Venturini S, Ferri R, Carrozzi M, Burlini F, Monti-Bragadin C.

Environ Mutagen. 1983;5(1):23-32.

PMID:
6339216

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