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

Year Number of Results
1993 2
1996 1
1997 1
2000 3
2001 4
2003 2
2004 3
2005 1
2006 1
2007 2
2008 2
2009 6
2010 5
2011 9
2012 13
2013 7
2014 8
2015 9
2016 4
2017 11
2018 3
2019 5
2020 4
2021 5
2022 5
2023 2

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103 results

Results by year

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Page 1
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
Van de Vondel L, De Winter J, Beijer D, Coarelli G, Wayand M, Palvadeau R, Pauly MG, Klein K, Rautenberg M, Guillot-Noël L, Deconinck T, Vural A, Ertan S, Dogu O, Uysal H, Brankovic V, Herzog R, Brice A, Durr A, Klebe S, Stock F, Bischoff AT, Rattay TW, Sobrido MJ, De Michele G, De Jonghe P, Klopstock T, Lohmann K, Zanni G, Santorelli FM, Timmerman V, Haack TB, Züchner S; PREPARE Consortium; Schüle R, Stevanin G, Synofzik M, Basak AN, Baets J. Van de Vondel L, et al. Among authors: sobrido mj. Mov Disord. 2022 Jun;37(6):1175-1186. doi: 10.1002/mds.28959. Epub 2022 Feb 12. Mov Disord. 2022. PMID: 35150594 Free PMC article.
Zebrafish Models of Autosomal Dominant Ataxias.
Quelle-Regaldie A, Sobrido-Cameán D, Barreiro-Iglesias A, Sobrido MJ, Sánchez L. Quelle-Regaldie A, et al. Among authors: sobrido mj. Cells. 2021 Feb 17;10(2):421. doi: 10.3390/cells10020421. Cells. 2021. PMID: 33671313 Free PMC article. Review.
Zebrafish Models of Autosomal Recessive Ataxias.
Quelle-Regaldie A, Sobrido-Cameán D, Barreiro-Iglesias A, Sobrido MJ, Sánchez L. Quelle-Regaldie A, et al. Among authors: sobrido mj. Cells. 2021 Apr 8;10(4):836. doi: 10.3390/cells10040836. Cells. 2021. PMID: 33917666 Free PMC article. Review.
Primary familial brain calcifications.
Quintáns B, Oliveira J, Sobrido MJ. Quintáns B, et al. Among authors: sobrido mj. Handb Clin Neurol. 2018;147:307-317. doi: 10.1016/B978-0-444-63233-3.00020-8. Handb Clin Neurol. 2018. PMID: 29325620 Review.
Primary Familial Brain Calcification.
Ramos EM, Oliveira J, Sobrido MJ, Coppola G. Ramos EM, et al. Among authors: sobrido mj. 2004 Apr 18 [updated 2017 Aug 24]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2004 Apr 18 [updated 2017 Aug 24]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301594 Free Books & Documents. Review.
Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia».
Arias M, García-Murias M, Sobrido MJ. Arias M, et al. Among authors: sobrido mj. Neurologia. 2017 Jul-Aug;32(6):386-393. doi: 10.1016/j.nrl.2014.11.005. Epub 2015 Jan 13. Neurologia. 2017. PMID: 25593102 Free article. Review. English, Spanish.
Applied and translational neurogenomics.
Sobrido MJ, Mohamed WM. Sobrido MJ, et al. Appl Transl Genom. 2015 Jun 23;5:1-2. doi: 10.1016/j.atg.2015.06.003. eCollection 2015 Jun 1. Appl Transl Genom. 2015. PMID: 26937351 Free PMC article. No abstract available.
Brain calcifications and PCDH12 variants.
Nicolas G, Sanchez-Contreras M, Ramos EM, Lemos RR, Ferreira J, Moura D, Sobrido MJ, Richard AC, Lopez AR, Legati A, Deleuze JF, Boland A, Quenez O, Krystkowiak P, Favrole P, Geschwind DH, Aran A, Segel R, Levy-Lahad E, Dickson DW, Coppola G, Rademakers R, de Oliveira JRM. Nicolas G, et al. Among authors: sobrido mj. Neurol Genet. 2017 Jul 26;3(4):e166. doi: 10.1212/NXG.0000000000000166. eCollection 2017 Aug. Neurol Genet. 2017. PMID: 28804758 Free PMC article.
103 results