Capra AP - Search Results

1

Primary anetoderma in a woman after ovarian stimulations for in vitro fertilization program.

Bellanca S, Musumeci ML, Catalano F, Cannarella R, Liuzzo C, Capra AP, Micali G. Bellanca S, et al. Among authors: capra ap. JAAD Case Rep. 2019 May 8;5(5):466-467. doi: 10.1016/j.jdcr.2019.03.004. eCollection 2019 May. JAAD Case Rep. 2019. PMID: 31193004 Free PMC article. No abstract available.

2

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: capra ap. 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.

3

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: capra ap. Pediatr Dev Pathol. 2018 Sep-Oct;21(5):456-460. doi: 10.1177/1093526618755200. Epub 2018 Feb 9. Pediatr Dev Pathol. 2018. PMID: 29426274

4

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: capra ap. Psychiatry Res. 2021 Mar;297:113729. doi: 10.1016/j.psychres.2021.113729. Epub 2021 Jan 21. Psychiatry Res. 2021. PMID: 33524775

5

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. 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.

6

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: capra ap. 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

7

Autoimmune hepatitis in genetic syndromes: A literature review.

Capra AP, Chiara E, Briuglia S. Capra AP, et al. World J Hepatol. 2021 Oct 27;13(10):1328-1340. doi: 10.4254/wjh.v13.i10.1328. World J Hepatol. 2021. PMID: 34786169 Free PMC article. Review.

8

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: capra ap. Genes (Basel). 2022 Jun 6;13(6):1019. doi: 10.3390/genes13061019. Genes (Basel). 2022. PMID: 35741781 Free PMC article.

9

A Systematic Review and Meta-Analysis of the Association between the FV H1299R Variant and the Risk of Recurrent Pregnancy Loss.

Capra AP, Ardizzone A, Briuglia S, La Rosa MA, Mondello S, Campolo M, Esposito E. Capra AP, et al. Biology (Basel). 2022 Nov 3;11(11):1608. doi: 10.3390/biology11111608. Biology (Basel). 2022. PMID: 36358309 Free PMC article. Review.

10

The Impact of COVID-19 on Amputation and Mortality Rates in Patients with Acute Limb Ischemia: A Systematic Review and Meta-Analysis.

Crupi L, Ardizzone A, Calapai F, Scuderi SA, Benedetto F, Esposito E, Capra AP. Crupi L, et al. Among authors: capra ap. Diseases. 2024 Apr 7;12(4):74. doi: 10.3390/diseases12040074. Diseases. 2024. PMID: 38667532 Free PMC article. Review.

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