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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2012 | 1 |
2013 | 1 |
2016 | 2 |
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2023 | 1 |
2024 | 0 |
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Page 1
Carboplatin and paclitaxel plus avelumab compared with carboplatin and paclitaxel in advanced or recurrent endometrial cancer (MITO END-3): a multicentre, open-label, randomised, controlled, phase 2 trial.
Lancet Oncol. 2023 Mar;24(3):286-296. doi: 10.1016/S1470-2045(23)00016-5. Epub 2023 Feb 14.
Lancet Oncol. 2023.
PMID: 37052965
Clinical Trial.
A novel MED12 mutation: Evidence for a fourth phenotype.
Prontera P, Ottaviani V, Rogaia D, Isidori I, Mencarelli A, Malerba N, Cocciadiferro D, Rolph P, Stangoni G, Vulto-van Silfhout A, Merla G.
Prontera P, et al. Among authors: isidori i.
Am J Med Genet A. 2016 Sep;170(9):2377-82. doi: 10.1002/ajmg.a.37805. Epub 2016 Jun 17.
Am J Med Genet A. 2016.
PMID: 27312080
Review.
Item in Clipboard
Xq12-q13.3 duplication: evidence of a recurrent syndrome.
Prontera P, Ottaviani V, Isidori I, Stangoni G, Donti E.
Prontera P, et al. Among authors: isidori i.
Ann Neurol. 2012 Nov;72(5):821-2; author reply 822-3. doi: 10.1002/ana.23754.
Ann Neurol. 2012.
PMID: 23280798
No abstract available.
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Aicardi syndrome associated with autosomal genomic imbalance: coincidence or evidence for autosomal inheritance with sex-limited expression?
Prontera P, Bartocci A, Ottaviani V, Isidori I, Rogaia D, Ardisia C, Guercini G, Mencarelli A, Donti E.
Prontera P, et al. Among authors: isidori i.
Mol Syndromol. 2013 Apr;4(4):197-202. doi: 10.1159/000350040. Epub 2013 Apr 11.
Mol Syndromol. 2013.
PMID: 23801936
Free PMC article.
Item in Clipboard
QF-PCR and MLPA: a reliable molecular system to detect chromosomal alterations in miscarriages.
Isidori I, Spapperi C, Barbati A, Mencarelli A, Stangoni G.
Isidori I, et al.
Clin Exp Obstet Gynecol. 2017;44(2):220-225.
Clin Exp Obstet Gynecol. 2017.
PMID: 29746026
Item in Clipboard
A Clinical and Molecular Survey of 62 Cystic Fibrosis Patients from Umbria (Central Italy) Disclosing a High Frequency (2.4%) of the 2184insA Allele: Implications for Screening.
Prontera P, Isidori I, Mencarini V, Pennoni G, Mencarelli A, Stangoni G, Di Cara G, Verrotti A.
Prontera P, et al. Among authors: isidori i.
Public Health Genomics. 2016;19(6):336-341. doi: 10.1159/000450849. Epub 2016 Oct 12.
Public Health Genomics. 2016.
PMID: 27728908
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Cleft palate and ADULT phenotype in a patient with a novel TP63 mutation suggests lumping of EEC/LM/ADULT syndromes into a unique entity: ELA syndrome.
Prontera P, Garelli E, Isidori I, Mencarelli A, Carando A, Silengo MC, Donti E.
Prontera P, et al. Among authors: isidori i.
Am J Med Genet A. 2011 Nov;155A(11):2746-9. doi: 10.1002/ajmg.a.34270. Epub 2011 Oct 11.
Am J Med Genet A. 2011.
PMID: 21990121
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