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161 results

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Page 1
Alemtuzumab-Related Lymphocyte Subset Dynamics and Disease Activity or Autoimmune Adverse Events: Real-World Evidence.
Signoriello E, Lus G, Saccà F, Puthenparampil M, Coppola C, Di Pietro A, Puoti G, Criscuolo MC, Foschi M, Miele G, Abbadessa G, Brescia Morra V, Gallo P, Bonavita S, Sormani MP, Signori A. Signoriello E, et al. Among authors: sacca f. J Clin Med. 2023 Feb 22;12(5):1768. doi: 10.3390/jcm12051768. J Clin Med. 2023. PMID: 36902555 Free PMC article.
Patient-reported burden of myasthenia gravis: baseline results of the international prospective, observational, longitudinal real-world digital study MyRealWorld-MG.
Dewilde S, Philips G, Paci S, Beauchamp J, Chiroli S, Quinn C, Day L, Larkin M, Palace J, Berrih-Aknin S, Claeys KG, Muppidi S, Mantegazza R, Saccà F, Meisel A, Bassez G, Murai H, Janssen MF. Dewilde S, et al. Among authors: sacca f. BMJ Open. 2023 Jan 31;13(1):e066445. doi: 10.1136/bmjopen-2022-066445. BMJ Open. 2023. PMID: 36720569 Free PMC article.
Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.
De Michele G, Pocchiari M, Petraroli R, Manfredi M, Caneve G, Coppola G, Casali C, Saccà F, Piccardo P, Salvatore E, Berardelli A, Orio M, Barbieri F, Ghetti B, Filla A. De Michele G, et al. Among authors: sacca f. Can J Neurol Sci. 2003 Aug;30(3):233-6. doi: 10.1017/s0317167100002651. Can J Neurol Sci. 2003. PMID: 12945948
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.
Coppola G, Criscuolo C, De Michele G, Striano S, Barbieri F, Striano P, Perretti A, Santoro L, Brescia Morra V, Saccà F, Scarano V, D'Adamo AP, Banfi S, Gasparini P, Santorelli FM, Lehesjoki AE, Filla A. Coppola G, et al. Among authors: sacca f. J Neurol. 2005 Aug;252(8):897-900. doi: 10.1007/s00415-005-0766-3. Epub 2005 Mar 8. J Neurol. 2005. PMID: 15742102
Very late onset in ataxia oculomotor apraxia type I.
Criscuolo C, Mancini P, Menchise V, Saccà F, De Michele G, Banfi S, Filla A. Criscuolo C, et al. Among authors: sacca f. Ann Neurol. 2005 May;57(5):777. doi: 10.1002/ana.20463. Ann Neurol. 2005. PMID: 15852392 Free article. No abstract available.
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.
Criscuolo C, Chessa L, Di Giandomenico S, Mancini P, Saccà F, Grieco GS, Piane M, Barbieri F, De Michele G, Banfi S, Pierelli F, Rizzuto N, Santorelli FM, Gallosti L, Filla A, Casali C. Criscuolo C, et al. Among authors: sacca f. Neurology. 2006 Apr 25;66(8):1207-10. doi: 10.1212/01.wnl.0000208402.10512.4a. Neurology. 2006. PMID: 16636238
161 results