个人简介
Maria Pia Manitto是一位眼科医生,主要研究遗传性眼部疾病和小儿眼科学(儿童眼部发育和疾病)。Manitto医生还是米兰圣拉斐尔研究医院的眼科顾问医师。
Manitto医生是意大利眼遗传学会(SIOG)的创始成员之一。
她发表了11篇关于遗传疾病(遗传性视网膜营养不良)的实验和临床论文。
出版物
最新出版物
Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art
2021 Oct 15;8:750586. doi: 10.3389/fmed.2021.750586. eCollection 2021. PMID: 34722588 Free PMC article. Review.
Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies
Ophthalmol Ther. 2020 Jun;9(2):249-263. doi: 10.1007/s40123-020-00241-1. Epub 2020 Mar 5. PMID: 32141037 Free PMC article. Review.
Benign foveal depigmentation: a multimodal imaging investigation
2023 Jan 1;17(1):74-79. doi: 10.1097/ICB.0000000000001115. PMID: 33395020
Multimodal imaging in Schubert-Bornschein congenital stationary night blindness
2022 Oct 13:1-6. doi: 10.1080/13816810.2022.2135108. Online ahead of print. PMID: 36226416
Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype
J Neuroophthalmol. 2021 Sep 1;41(3):e290-e292. doi: 10.1097/WNO.0000000000001124. PMID: 33136666 No abstract available.
Morpho-functional correlation of fundus autofluorescence in Stargardt disease
Br J Ophthalmol. 2015 Oct;99(10):1354-9. doi: 10.1136/bjophthalmol-2014-306237. Epub 2015 Apr 2. PMID: 25837607
Vascular alterations revealed with optical coherence tomography angiography in patients with choroideremia
Retina. 2019 Jun;39(6):1200-1205. doi: 10.1097/IAE.0000000000002118. PMID: 29543633 Page 2
Capillary network alterations in x-linked retinoschisis imaged on optical coherence tomography angiography
Retina. 2019 Sep;39(9):1761-1767. doi: 10.1097/IAE.0000000000002222. PMID: 29877903
Posterior polymorphous corneal dystrophy concomitant to large colloid drusen
Eur J Ophthalmol. 2015 Mar-Apr;25(2):177-9. doi: 10.5301/ejo.5000526. Epub 2014 Oct 8. PMID: 25363852
Spectral domain optical coherence tomography findings in patients with retinitis pigmentosa
Ophthalmic Res. 2013;50(3):160-4. doi: 10.1159/000351681. Epub 2013 Aug 28. PMID: 23989166
Clinical Utility Gene Card for: autosomal recessive cone-rod dystrophy
Eur J Hum Genet. 2015 Dec;23(12):1749-. doi: 10.1038/ejhg.2015.67. Epub 2015 Apr 15. PMID: 25873014 Free PMC article. No abstract available.
Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches
EJIFCC. 2018 Apr 30;29(1):15-25. eCollection 2018 Apr. PMID: 29765283 Free PMC article.
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients
Mol Vis. 2011;17:3078-87. Epub 2011 Nov 24. PMID: 22162627 Free PMC article.
De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy
Clin Chem Lab Med. 2006;44(5):533-7. doi: 10.1515/CCLM.2006.116. PMID: 16681420