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2016 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
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Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Genet Med. 2020 Nov;22(11):1851-1862. doi: 10.1038/s41436-020-0899-x. Epub 2020 Jul 27.
Genet Med. 2020.
PMID: 32713943
Free article.
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Roux T, Barbier M, Papin M, Davoine CS, Sayah S, Coarelli G, Charles P, Marelli C, Parodi L, Tranchant C, Goizet C, Klebe S, Lohmann E, Van Maldergem L, van Broeckhoven C, Coutelier M, Tesson C, Stevanin G, Duyckaerts C, Brice A, Durr A; SPATAX network.
Roux T, et al.
Genet Med. 2021 Oct;23(10):2021. doi: 10.1038/s41436-020-01064-y.
Genet Med. 2021.
PMID: 33353973
Free article.
No abstract available.
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Discordance in pathology report after central pathology review: Implications for breast cancer adjuvant treatment.
Orlando L, Viale G, Bria E, Lutrino ES, Sperduti I, Carbognin L, Schiavone P, Quaranta A, Fedele P, Caliolo C, Calvani N, Criscuolo M, Cinieri S.
Orlando L, et al.
Breast. 2016 Dec;30:151-155. doi: 10.1016/j.breast.2016.09.015. Epub 2016 Oct 14.
Breast. 2016.
PMID: 27750105
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