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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Brain. 2021 Jun 22;144(5):1422-1434. doi: 10.1093/brain/awab041.
Brain. 2021.
PMID: 33970200
Free PMC article.
Epilepsy in LAMA2-related muscular dystrophy: A systematic review of the literature.
Salvati A, Bonaventura E, Sesso G, Pasquariello R, Sicca F.
Salvati A, et al. Among authors: pasquariello r.
Seizure. 2021 Oct;91:425-436. doi: 10.1016/j.seizure.2021.07.020. Epub 2021 Jul 21.
Seizure. 2021.
PMID: 34325301
Free article.
Review.
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Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
Wiessner M, Maroofian R, Ni MY, Pedroni A, Müller JS, Stucka R, Beetz C, Efthymiou S, Santorelli FM, Alfares AA, Zhu C, Uhrova Meszarosova A, Alehabib E, Bakhtiari S, Janecke AR, Otero MG, Chen JYH, Peterson JT, Strom TM, De Jonghe P, Deconinck T, De Ridder W, De Winter J, Pasquariello R, Ricca I, Alfadhel M, van de Warrenburg BP, Portier R, Bergmann C, Ghasemi Firouzabadi S, Jin SC, Bilguvar K, Hamed S, Abdelhameed M, Haridy NA, Maqbool S, Rahman F, Anwar N, Carmichael J, Pagnamenta AT, Wood NW, Tran Mau-Them F, Haack T; Genomics England Research Consortium, PREPARE network; Di Rocco M, Ceccherini I, Iacomino M, Zara F, Salpietro V, Scala M, Rusmini M, Xu Y, Wang Y, Suzuki Y, Koh K, Nan H, Ishiura H, Tsuji S, Lambert L, Schmitt E, Lacaze E, Küpper H, Dredge D, Skraban C, Goldstein A, Willis MJH, Grand K, Graham JM, Lewis RA, Millan F, Duman Ö, Olgac Dundar N, Uyanik G, Schöls L, Nürnberg P, Nürnberg G, Català-Bordes A, Seeman P, Kuchar M, Darvish H, Rebelo A, Bouçanova F, Medard JJ, Chrast R, Auer-Grumbach M, Alkuraya FS, Shamseldin H, Al Tala S, Rezazadeh Varaghchi J, Najafi M, Deschner S, Gläser D, Hüttel W, Kruer MC, Kamsteeg EJ, Takiyama Y, Züchner S, Baets J, Synofzik…
See abstract for full author list ➔
Wiessner M, et al. Among authors: pasquariello r.
Brain. 2021 Sep 4;144(8):e70. doi: 10.1093/brain/awab193.
Brain. 2021.
PMID: 34480796
Free PMC article.
No abstract available.
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