La Rosa MA - 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: la rosa ma. Genes (Basel). 2022 Apr 27;13(5):780. doi: 10.3390/genes13050780. Genes (Basel). 2022. PMID: 35627165 Free PMC article. Review.

2

A child with severe iron-deficiency anemia and a complex TMPRSS6 genotype.

Capra AP, Ferro E, Cannavò L, La Rosa MA, Zirilli G. Capra AP, et al. Among authors: la rosa ma. Hematology. 2017 Oct;22(9):559-564. doi: 10.1080/10245332.2017.1317990. Epub 2017 Apr 27. Hematology. 2017. PMID: 28447549 Free article.

3

A Novel Mutation of the δ-Globin Gene in an Asymptomatic 30-Year-Old Female.

Di Bella C, Pugliatti F, La Rosa MA, Cara S, Capra AP, Rigoli L. Di Bella C, et al. Among authors: la rosa ma. Acta Haematol. 2018;139(1):33-34. doi: 10.1159/000484973. Epub 2018 Jan 13. Acta Haematol. 2018. PMID: 29332098 Free article. No abstract available.

4

FTL c.-168G>C Mutation in Hereditary Hyperferritinemia Cataract Syndrome: A New Italian Family.

Ferro E, Capra AP, Zirilli G, Meduri A, Urso M, Briuglia S, La Rosa MA. Ferro E, et al. Among authors: la rosa ma. Pediatr Dev Pathol. 2018 Sep-Oct;21(5):456-460. doi: 10.1177/1093526618755200. Epub 2018 Feb 9. Pediatr Dev Pathol. 2018. PMID: 29426274

5

Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion.

Capra AP, Ferro E, La Rosa MA, Briuglia S, Russo T, Arena S, Salpietro Damiano C, Romeo C, Impellizzeri P. Capra AP, et al. Among authors: la rosa ma. Pediatr Surg Int. 2018 Jul;34(7):807-812. doi: 10.1007/s00383-018-4280-y. Epub 2018 May 21. Pediatr Surg Int. 2018. PMID: 29785651

6

Correspondence on "Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies" by Fountain et al.

Capra AP, Agolini E, La Rosa MA, Novelli A, Briuglia S. Capra AP, et al. Among authors: la rosa ma. Genet Med. 2021 Feb;23(2):421-422. doi: 10.1038/s41436-020-00978-x. Epub 2020 Oct 5. Genet Med. 2021. PMID: 33012787 Free article. No abstract available.

7

Molecular Pathways within Autism Spectrum Disorder Endophenotypes.

Briuglia S, Calabrò M, Capra AP, Briguori S, La Rosa MA, Crisafulli C. Briuglia S, et al. Among authors: la rosa ma. J Mol Neurosci. 2021 Jul;71(7):1357-1367. doi: 10.1007/s12031-020-01782-7. Epub 2021 Jan 25. J Mol Neurosci. 2021. PMID: 33492615

8

CNVs inform the biological network of Autism spectrum disorder.

Briuglia S, Calabrò M, Capra AP, La Rosa MA, Crisafulli C. Briuglia S, et al. Among authors: la rosa ma. Psychiatry Res. 2021 Mar;297:113729. doi: 10.1016/j.psychres.2021.113729. Epub 2021 Jan 21. Psychiatry Res. 2021. PMID: 33524775

9

[No title available]

[No authors listed] [No authors listed] PMID: 35557144

10

H1299R Variant in Factor V and Recurrent Pregnancy Loss: A Systematic Review and Meta-Analysis Protocol.

Ardizzone A, Capra AP, Mondello S, Briuglia S, La Rosa MA, Campolo M, Esposito E. Ardizzone A, et al. Among authors: la rosa ma. Genes (Basel). 2022 Jun 6;13(6):1019. doi: 10.3390/genes13061019. Genes (Basel). 2022. PMID: 35741781 Free PMC article.

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