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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1995 7
1998 2
2000 1
2001 2
2002 3
2003 3
2004 3
2005 3
2006 2
2007 1
2009 1
2010 4
2011 2
2012 4
2013 3
2014 10
2015 5
2016 4
2017 12
2018 14
2019 17
2020 14
2021 16
2022 5
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Search Results

128 results
Results by year
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Page 1
Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls.
Darras BT, Masson R, Mazurkiewicz-Bełdzińska M, Rose K, Xiong H, Zanoteli E, Baranello G, Bruno C, Vlodavets D, Wang Y, El-Khairi M, Gerber M, Gorni K, Khwaja O, Kletzl H, Scalco RS, Fontoura P, Servais L; FIREFISH Working Group. Darras BT, et al. Among authors: zanoteli e. N Engl J Med. 2021 Jul 29;385(5):427-435. doi: 10.1056/NEJMoa2102047. N Engl J Med. 2021. PMID: 34320287
Rhabdomyolysis: a genetic perspective.
Scalco RS, Gardiner AR, Pitceathly RD, Zanoteli E, Becker J, Holton JL, Houlden H, Jungbluth H, Quinlivan R. Scalco RS, et al. Among authors: zanoteli e. Orphanet J Rare Dis. 2015 May 2;10:51. doi: 10.1186/s13023-015-0264-3. Orphanet J Rare Dis. 2015. PMID: 25929793 Free PMC article. Review.
Therapeutic advances in 5q-linked spinal muscular atrophy.
Reed UC, Zanoteli E. Reed UC, et al. Among authors: zanoteli e. Arq Neuropsiquiatr. 2018 Apr;76(4):265-272. doi: 10.1590/0004-282x20180011. Arq Neuropsiquiatr. 2018. PMID: 29742241 Free article. Review.
Severe progressive brain involvement in a patient with TRMT10C mutation.
Camelo CG, Silva AMS, Rocha AJ, Scaramuzzi V, Moreno CAM, Reed UC, Zanoteli E. Camelo CG, et al. Among authors: zanoteli e. Arq Neuropsiquiatr. 2021 Mar;79(3):259-260. doi: 10.1590/0004-282X-ANP-2020-0355. Arq Neuropsiquiatr. 2021. PMID: 33886802 Free article. No abstract available.
A Novel Multisystem Proteinopathy Caused by a Missense ANXA11 Variant.
Leoni TB, González-Salazar C, Rezende TJR, Hernández ALC, Mattos AHB, Coimbra Neto AR, da Graça FF, Gonçalves JPN, Martinez ARM, Taniguti L, Kitajima JP, Kok F, Rogério F, da Silva AMS, de Oliveira ALR, Zanoteli E, Nucci A, França MC Jr. Leoni TB, et al. Among authors: zanoteli e. Ann Neurol. 2021 Aug;90(2):239-252. doi: 10.1002/ana.26136. Epub 2021 Jun 14. Ann Neurol. 2021. PMID: 34048612
Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis.
Carneiro A, Viana-Gomes D, Macedo-da-Silva J, Lima GHO, Mitri S, Alves SR, Kolliari-Turner A, Zanoteli E, Neto FRA, Palmisano G, Pesquero JB, Moreira JC, Pereira MD. Carneiro A, et al. Among authors: zanoteli e. Neuromuscul Disord. 2021 Jul;31(7):583-595. doi: 10.1016/j.nmd.2021.04.007. Epub 2021 May 6. Neuromuscul Disord. 2021. PMID: 34193371 Review.
International retrospective natural history study of LMNA-related congenital muscular dystrophy.
Ben Yaou R, Yun P, Dabaj I, Norato G, Donkervoort S, Xiong H, Nascimento A, Maggi L, Sarkozy A, Monges S, Bertoli M, Komaki H, Mayer M, Mercuri E, Zanoteli E, Castiglioni C, Marini-Bettolo C, D'Amico A, Deconinck N, Desguerre I, Erazo-Torricelli R, Gurgel-Giannetti J, Ishiyama A, Kleinsteuber KS, Lagrue E, Laugel V, Mercier S, Messina S, Politano L, Ryan MM, Sabouraud P, Schara U, Siciliano G, Vercelli L, Voit T, Yoon G, Alvarez R, Muntoni F, Pierson TM, Gómez-Andrés D, Reghan Foley A, Quijano-Roy S, Bönnemann CG, Bonne G. Ben Yaou R, et al. Among authors: zanoteli e. Brain Commun. 2021 Apr 11;3(3):fcab075. doi: 10.1093/braincomms/fcab075. eCollection 2021 Jul. Brain Commun. 2021. PMID: 34240052 Free PMC article.
Myasthenia Gravis and COVID-19: Clinical Characteristics and Outcomes.
Camelo-Filho AE, Silva AMS, Estephan EP, Zambon AA, Mendonça RH, Souza PVS, Pinto WBVR, Oliveira ASB, Dangoni-Filho I, Pouza AFP, Valerio BCO, Zanoteli E. Camelo-Filho AE, et al. Among authors: zanoteli e. Front Neurol. 2020 Sep 11;11:1053. doi: 10.3389/fneur.2020.01053. eCollection 2020. Front Neurol. 2020. PMID: 33013676 Free PMC article.
128 results