Carrozzi M - Search Results

1

TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition.

Musante L, Faletra F, Meier K, Tomoum H, Najarzadeh Torbati P, Blair E, North S, Gärtner J, Diegmann S, Beiraghi Toosi M, Ashrafzadeh F, Ghayoor Karimiani E, Murphy D, Murru FM, Zanus C, Magnolato A, La Bianca M, Feresin A, Girotto G, Gasparini P, Costa P, Carrozzi M. Musante L, et al. Among authors: carrozzi m. Am J Med Genet A. 2022 Sep;188(9):2652-2665. doi: 10.1002/ajmg.a.62852. Epub 2022 Jun 7. Am J Med Genet A. 2022. PMID: 35670379 Free PMC article.

2

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. Demori E, et al. Among authors: carrozzi m. Am J Med Genet A. 2004 Oct 15;130A(3):288-94. doi: 10.1002/ajmg.a.20677. Am J Med Genet A. 2004. PMID: 15378554 Review.

3

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

Benussi DG, Costa P, Zollino M, Murdolo M, Petix V, Carrozzi M, Pecile V. Benussi DG, et al. Among authors: carrozzi m. Genet Test Mol Biomarkers. 2009 Apr;13(2):199-204. doi: 10.1089/gtmb.2008.0109. Genet Test Mol Biomarkers. 2009. PMID: 19378504

4

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

Zanus C, Furlan C, Costa P, Cosentini D, Carrozzi M. Zanus C, et al. Among authors: carrozzi m. Cephalalgia. 2009 Nov;29(11):1232-7. doi: 10.1111/j.1468-2982.2009.01856.x. Epub 2009 Apr 9. Cephalalgia. 2009. PMID: 19558537

5

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. Faletra F, et al. Among authors: carrozzi m. J Appl Genet. 2011 Feb;52(1):77-80. doi: 10.1007/s13353-010-0004-2. Epub 2010 Nov 3. J Appl Genet. 2011. PMID: 21107783 No abstract available.

6

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. Faletra F, et al. Among authors: carrozzi m. Am J Med Genet A. 2012 Feb;158A(2):461-4. doi: 10.1002/ajmg.a.34398. Epub 2011 Dec 2. Am J Med Genet A. 2012. PMID: 22140086 No abstract available.

7

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

Zanus C, Alberini E, Costa P, Colonna F, Zennaro F, Carrozzi M. Zanus C, et al. Among authors: carrozzi m. Epileptic Disord. 2012 Jun;14(2):174-80. doi: 10.1684/epd.2012.0507. Epileptic Disord. 2012. PMID: 22591802 Free article.

8

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. Bortot B, et al. Among authors: carrozzi m. Gene. 2013 Dec 1;531(2):506-9. doi: 10.1016/j.gene.2013.07.083. Epub 2013 Aug 26. Gene. 2013. PMID: 23988505

9

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. Parisi P, et al. Among authors: carrozzi m. Seizure. 2015 Sep;31:56-63. doi: 10.1016/j.seizure.2015.07.005. Epub 2015 Jul 17. Seizure. 2015. PMID: 26362378 Free article.

10

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. Zanus C, et al. Among authors: carrozzi m. PLoS One. 2017 Jan 26;12(1):e0170979. doi: 10.1371/journal.pone.0170979. eCollection 2017. PLoS One. 2017. PMID: 28125701 Free PMC article.

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