Zoia S, Biancotto M, Guicciardi M, Lecis R, Lucidi F, Pelamatti GM, Carrozzi M, Skabar A, Sugden DA, Barnett AL, Henderson SE. An evaluation of the Movement ABC-2 Test for use in Italy: A comparison of data from Italy and the UK. Res Dev Disabil 2019;84:43-56.

Zanus C, Battistutta S, Aliverti R, Montico M, Cremaschi S, Ronfani L, Monasta L, Carrozzi M. Adolescent Admissions to Emergency Departments for Self-Injurious Thoughts and Behaviors. PLoS One 2017;12(1):e0170979.

Abate MValentina, Stocco G, Devescovi R, Carrozzi M, Pierobon C, Valencic E, Lucafò M, Di Silvestre A, d'Adamo P, Tommasini A, Decorti G, Ventura A. Carbamazepine-induced thrombocytopenic purpura in a child: Insights from a genomic analysis. Blood Cells Mol Dis 2016;59:97-9.

Devescovi R, Monasta L, Mancini A, Bin M, Vellante V, Carrozzi M, Colombi C. Early diagnosis and Early Start Denver Model intervention in autism spectrum disorders delivered in an Italian Public Health System service. Neuropsychiatr Dis Treat 2016;12:1379-84.

Alberini E, Vellante V, Zennaro F, Calligaris L, Barbi E, Carrozzi M, Devescovi R. Acute pseudotumoral hemicerebellitis in a child: a rare and distinct entity?. J Child Neurol 2015;30(4):496-9.

Parisi P, Verrotti A, Costa P, Striano P, Zanus C, Carrozzi M, Raucci U, Villa MPia, Belcastro V. Diagnostic criteria currently proposed for "ictal epileptic headache": Perspectives on strengths, weaknesses and pitfalls. Seizure 2015;31:56-63.

Faletra F, d'Adamo APio, Rocca MSanta, Carrozzi M, Perrone MDolores, Pecile V, Gasparini P. Does the 1.5?Mb microduplication in chromosome band Xp22.31 have a pathogenetic role? New contribution and a review of the literature. Am J Med Genet A 2012;158A(2):461-4.

Zorzi M, Barbiero C, Facoetti A, Lonciari I, Carrozzi M, Montico M, Bravar L, George F, Pech-Georgel C, Ziegler JC. Extra-large letter spacing improves reading in dyslexia. Proc Natl Acad Sci U S A 2012;109(28):11455-9.

Zanus C, Alberini E, Costa P, Colonna F, Zennaro F, Carrozzi M. Involuntary movements after correction of vitamin B12 deficiency: a video-case report. Epileptic Disord 2012;14(2):174-80.

Carrozzi M, Amaddeo A, Biondi A, Zanus C, Monti F, Alessandro V. Stem cells in severe infantile spinal muscular atrophy (SMA1). Neuromuscul Disord 2012;22(11):1032-4.

Barbiero C, Lonciari I, Montico M, Monasta L, Penge R, Vio C, Tressoldi PEmanuele, Ferluga V, Bigoni A, Tullio A, Carrozzi M, Ronfani L. The submerged dyslexia iceberg: how many school children are not diagnosed? Results from an Italian study. PLoS One 2012;7(10):e48082.

Biancotto M, Skabar A, Bulgheroni M, Carrozzi M, Zoia S. Neuromotor deficits in developmental coordination disorder: evidence from a reach-to-grasp task. Res Dev Disabil 2011;32(4):1293-300.

Faletra F, Devescovi R, Pecile V, Fabretto A, Carrozzi M, Gasparini P. A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature. J Appl Genet 2011;52(1):77-80.

Biffi S, Bortot B, Carrozzi M, Severini GMaria. Quantification of heteroplasmic mitochondrial DNA mutations for DNA samples in the low picogram range by nested real-time ARMS-qPCR. Diagn Mol Pathol 2011;20(2):117-22.