Malacarne M - Search Results

1

12q21 Interstitial Deletions: Seven New Syndromic Cases Detected by Array-CGH and Review of the Literature.

Recalcati MP, Catusi I, Garzo M, Redaelli S, Massimello M, Maitz SB, Gentile M, Ponzi E, Orsini P, Zilio A, Montaldi A, Calò A, Capra AP, Briuglia S, La Rosa MA, Grillo L, Romano C, Bianca S, Malacarne M, Busè M, Piccione M, Larizza L. Recalcati MP, et al. Among authors: malacarne m. Genes (Basel). 2022 Apr 27;13(5):780. doi: 10.3390/genes13050780. Genes (Basel). 2022. PMID: 35627165 Free PMC article. Review.

2

Perlman syndrome: clinical report and nine-year follow-up.

Piccione M, Cecconi M, Giuffrè M, Lo Curto M, Malacarne M, Piro E, Riccio A, Corsello G. Piccione M, et al. Among authors: malacarne m. Am J Med Genet A. 2005 Dec 1;139A(2):131-5. doi: 10.1002/ajmg.a.30994. Am J Med Genet A. 2005. PMID: 16278893

3

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.

Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F. Elia M, et al. Among authors: malacarne m. Epilepsia. 2006 May;47(5):830-8. doi: 10.1111/j.1528-1167.2006.00522.x. Epilepsia. 2006. PMID: 16686647 Free article.

4

10qter deletion: a new case.

Piccione M, Antona V, Piro E, Cavani S, Malacarne M, Pierluigi M, Corsello G. Piccione M, et al. Among authors: malacarne m. Am J Med Genet A. 2008 Sep 15;146A(18):2435-8. doi: 10.1002/ajmg.a.32467. Am J Med Genet A. 2008. PMID: 18698621 No abstract available.

5

Array CGH defined interstitial deletion on chromosome 14: a new case.

Piccione M, Antona V, Scavone V, Malacarne M, Pierluigi M, Grasso M, Corsello G. Piccione M, et al. Among authors: malacarne m. Eur J Pediatr. 2010 Jul;169(7):845-51. doi: 10.1007/s00431-009-1128-4. Epub 2010 Jan 21. Eur J Pediatr. 2010. PMID: 20087602

6

Array-CGH defined chromosome 1p duplication in a patient with autism spectrum disorder, mild mental deficiency, and minor dysmorphic features.

Piccione M, Antona V, Antona R, Gambino G, Pierluigi M, Malacarne M, Cavani S, Corsello G. Piccione M, et al. Among authors: malacarne m. Am J Med Genet A. 2010 Feb;152A(2):486-9. doi: 10.1002/ajmg.a.33212. Am J Med Genet A. 2010. PMID: 20101695 No abstract available.

7

The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication.

Piccione M, Vecchio D, Cavani S, Malacarne M, Pierluigi M, Corsello G. Piccione M, et al. Among authors: malacarne m. Am J Med Genet A. 2011 Dec;155A(12):3054-9. doi: 10.1002/ajmg.a.34275. Epub 2011 Oct 14. Am J Med Genet A. 2011. PMID: 22002912

8

Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders.

Piccione M, Sanfilippo C, Cavani S, Salatiello P, Malacarne M, Pierluigi M, Fichera M, Luciano D, Corsello G. Piccione M, et al. Among authors: malacarne m. J Genet. 2011 Dec;90(3):473-7. doi: 10.1007/s12041-011-0096-4. J Genet. 2011. PMID: 22227935 No abstract available.

9

Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation.

Piccione M, Piro E, Serraino F, Cavani S, Ciccone R, Malacarne M, Pierluigi M, Vitaloni M, Zuffardi O, Corsello G. Piccione M, et al. Among authors: malacarne m. Eur J Med Genet. 2012 Apr;55(4):238-44. doi: 10.1016/j.ejmg.2012.01.014. Epub 2012 Feb 18. Eur J Med Genet. 2012. PMID: 22406401

10

Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH.

Viaggi CD, Cavani S, Pierluigi M, Antona V, Piro E, Corsello G, Mogni M, Piccione M, Malacarne M. Viaggi CD, et al. Among authors: malacarne m. J Appl Genet. 2012 Aug;53(3):285-8. doi: 10.1007/s13353-012-0097-x. Epub 2012 Apr 29. J Appl Genet. 2012. PMID: 22544656

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