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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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2009 | 1 |
2015 | 1 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
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Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients.
Genes (Basel). 2020 Jun 19;11(6):671. doi: 10.3390/genes11060671.
Genes (Basel). 2020.
PMID: 32575496
Free PMC article.
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent Cohort.
Melloni G, Eoli M, Cesaretti C, Bianchessi D, Ibba MC, Esposito S, Scuvera G, Morcaldi G, Micheli R, Piozzi E, Avignone S, Chiapparini L, Pantaleoni C, Natacci F, Finocchiaro G, Saletti V.
Melloni G, et al. Among authors: ibba mc.
Cancers (Basel). 2019 Nov 21;11(12):1838. doi: 10.3390/cancers11121838.
Cancers (Basel). 2019.
PMID: 31766501
Free PMC article.
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126 novel mutations in Italian patients with neurofibromatosis type 1.
Bianchessi D, Morosini S, Saletti V, Ibba MC, Natacci F, Esposito S, Cesaretti C, Riva D, Finocchiaro G, Eoli M.
Bianchessi D, et al. Among authors: ibba mc.
Mol Genet Genomic Med. 2015 Jul 7;3(6):513-25. doi: 10.1002/mgg3.161. eCollection 2015 Nov.
Mol Genet Genomic Med. 2015.
PMID: 26740943
Free PMC article.
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Dizziness in patients with recent episodes of benign paroxysmal positional vertigo: real otolithic dysfunction or mental stress?
Faralli M, Ricci G, Ibba MC, Crognoletti M, Longari F, Frenguelli A.
Faralli M, et al. Among authors: ibba mc.
J Otolaryngol Head Neck Surg. 2009 Jun;38(3):375-80.
J Otolaryngol Head Neck Surg. 2009.
PMID: 19476771
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