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Year | Number of Results |
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2014 | 1 |
2015 | 3 |
2021 | 2 |
2024 | 0 |
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Page 1
Unique genomic profile associated with pediatric uveal melanoma.
Eur J Ophthalmol. 2015 Jul-Aug;25(4):e31-4. doi: 10.5301/ejo.5000600.
Eur J Ophthalmol. 2015.
PMID: 25790812
Diagnostic Yield and Cost-Effectiveness of "Dynamic" Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern Italy.
Varesio C, Gana S, Asaro A, Ballante E, Cabini RF, Tartara E, Bagnaschi M, Pasca L, Valente M, Orcesi S, Cereda C, Veggiotti P, Borgatti R, Valente EM, De Giorgis V.
Varesio C, et al. Among authors: asaro a.
Diagnostics (Basel). 2021 May 25;11(6):948. doi: 10.3390/diagnostics11060948.
Diagnostics (Basel). 2021.
PMID: 34070668
Free PMC article.
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A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset.
De Rose DU, Gallini F, Battaglia DI, Tiberi E, Gaudino S, Contaldo I, Veredice C, Romeo DM, Massimi L, Asaro A, Cereda C, Vento G, Mercuri EM.
De Rose DU, et al. Among authors: asaro a.
Neurol Sci. 2021 Nov;42(11):4759-4765. doi: 10.1007/s10072-021-05480-z. Epub 2021 Jul 22.
Neurol Sci. 2021.
PMID: 34292449
Free PMC article.
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Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
Zollino M, Orteschi D, Ruiter M, Pfundt R, Steindl K, Cafiero C, Ricciardi S, Contaldo I, Chieffo D, Ranalli D, Acquafondata C, Murdolo M, Marangi G, Asaro A, Battaglia D.
Zollino M, et al. Among authors: asaro a.
Epilepsia. 2014 Jun;55(6):849-57. doi: 10.1111/epi.12617. Epub 2014 Apr 16.
Epilepsia. 2014.
PMID: 24738919
Free article.
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Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.
Cafiero C, Marangi G, Orteschi D, Ali M, Asaro A, Ponzi E, Moncada A, Ricciardi S, Murdolo M, Mancano G, Contaldo I, Leuzzi V, Battaglia D, Mercuri E, Slavotinek AM, Zollino M.
Cafiero C, et al. Among authors: asaro a.
Eur J Hum Genet. 2015 Nov;23(11):1499-504. doi: 10.1038/ejhg.2015.19. Epub 2015 Feb 25.
Eur J Hum Genet. 2015.
PMID: 25712080
Free PMC article.
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Variable expressivity of a familial 1.9 Mb microdeletion in 3q28 leading to haploinsufficiency of TP63: Refinement of the critical region for a new microdeletion phenotype.
Ponzi E, Asaro A, Orteschi D, Genuardi M, Zollino M, Gurrieri F.
Ponzi E, et al. Among authors: asaro a.
Eur J Med Genet. 2015 Aug;58(8):400-5. doi: 10.1016/j.ejmg.2015.06.001. Epub 2015 Jun 24.
Eur J Med Genet. 2015.
PMID: 26117585
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