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

Year Number of Results
2007 2
2008 1
2009 2
2010 3
2012 2
2013 2
2014 1
2015 2
2016 6
2017 3
2018 6
2019 11
2020 15
2021 15
2022 17
2023 12

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88 results

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Page 1
Autoantibody screening in Guillain-Barré syndrome.
Lleixà C, Martín-Aguilar L, Pascual-Goñi E, Franco T, Caballero M, de Luna N, Gallardo E, Suárez-Calvet X, Martínez-Martínez L, Diaz-Manera J, Rojas-García R, Cortés-Vicente E, Turón J, Casasnovas C, Homedes C, Gutiérrez-Gutiérrez G, Jimeno-Montero MC, Berciano J, Sedano-Tous MJ, García-Sobrino T, Pardo-Fernández J, Márquez-Infante C, Rojas-Marcos I, Jericó-Pascual I, Martínez-Hernández E, Morís de la Tassa G, Domínguez-González C, Juárez C, Illa I, Querol L. Lleixà C, et al. Among authors: dominguez gonzalez c. J Neuroinflammation. 2021 Nov 1;18(1):251. doi: 10.1186/s12974-021-02301-0. J Neuroinflammation. 2021. PMID: 34719386 Free PMC article.
Genotype-phenotype correlations in valosin-containing protein disease: a retrospective muticentre study.
Schiava M, Ikenaga C, Villar-Quiles RN, Caballero-Ávila M, Topf A, Nishino I, Kimonis V, Udd B, Schoser B, Zanoteli E, Souza PVS, Tasca G, Lloyd T, Lopez-de Munain A, Paradas C, Pegoraro E, Nadaj-Pakleza A, De Bleecker J, Badrising U, Alonso-Jiménez A, Kostera-Pruszczyk A, Miralles F, Shin JH, Bevilacqua JA, Olivé M, Vorgerd M, Kley R, Brady S, Williams T, Domínguez-González C, Papadimas GK, Warman-Chardon J, Claeys KG, de Visser M, Muelas N, LaForet P, Malfatti E, Alfano LN, Nair SS, Manousakis G, Kushlaf HA, Harms MB, Nance C, Ramos-Fransi A, Rodolico C, Hewamadduma C, Cetin H, García-García J, Pál E, Farrugia ME, Lamont PJ, Quinn C, Nedkova-Hristova V, Peric S, Luo S, Oldfors A, Taylor K, Ralston S, Stojkovic T, Weihl C, Diaz-Manera J; VCP International Study Group; VCP International Study Group. Schiava M, et al. Among authors: dominguez gonzalez c. J Neurol Neurosurg Psychiatry. 2022 Jul 27:jnnp-2022-328921. doi: 10.1136/jnnp-2022-328921. Online ahead of print. J Neurol Neurosurg Psychiatry. 2022. PMID: 35896379
Making sense of missense variants in TTN-related congenital myopathies.
Rees M, Nikoopour R, Fukuzawa A, Kho AL, Fernandez-Garcia MA, Wraige E, Bodi I, Deshpande C, Özdemir Ö, Daimagüler HS, Pfuhl M, Holt M, Brandmeier B, Grover S, Fluss J, Longman C, Farrugia ME, Matthews E, Hanna M, Muntoni F, Sarkozy A, Phadke R, Quinlivan R, Oates EC, Schröder R, Thiel C, Reimann J, Voermans N, Erasmus C, Kamsteeg EJ, Konersman C, Grosmann C, McKee S, Tirupathi S, Moore SA, Wilichowski E, Hobbiebrunken E, Dekomien G, Richard I, Van den Bergh P, Domínguez-González C, Cirak S, Ferreiro A, Jungbluth H, Gautel M. Rees M, et al. Among authors: dominguez gonzalez c. Acta Neuropathol. 2021 Mar;141(3):431-453. doi: 10.1007/s00401-020-02257-0. Epub 2021 Jan 15. Acta Neuropathol. 2021. PMID: 33449170 Free PMC article.
[Myotonic dystrophy and primary care].
Domínguez-González C. Domínguez-González C. Semergen. 2020 Oct;46(7):439-440. doi: 10.1016/j.semerg.2020.09.001. Epub 2020 Oct 7. Semergen. 2020. PMID: 33039262 Spanish. No abstract available.
[Cognitive impairment in myotonic dystrophy type 1 (Steinert's disease)].
Rosado Bartolomé A, Puertas Martín V, Domínguez González C, Ramos Miranda M. Rosado Bartolomé A, et al. Among authors: dominguez gonzalez c. Semergen. 2022 Apr;48(3):208-213. doi: 10.1016/j.semerg.2022.01.013. Epub 2022 Mar 12. Semergen. 2022. PMID: 35292189 Review. Spanish.
[Steinert's disease and refusal to treatment].
Rosado-Bartolomé A, Domínguez-González C. Rosado-Bartolomé A, et al. Among authors: dominguez gonzalez c. Rev Neurol. 2021 Sep 1;73(5):184-185. doi: 10.33588/rn.7305.2021257. Rev Neurol. 2021. PMID: 34328207 Free article. Spanish.
[Orthostatic tremor: an enigmatic condition].
Labiano-Fontcuberta A, Benito-Leon J, Dominguez-Gonzalez C. Labiano-Fontcuberta A, et al. Among authors: dominguez gonzalez c. Rev Neurol. 2012 Apr 1;54(7):425-34. Rev Neurol. 2012. PMID: 22451130 Free article. Review. Spanish.
CMT4J, parkinsonism and a new FIG4 mutation.
Posada IJ, Domínguez-González C. Posada IJ, et al. Among authors: dominguez gonzalez c. Parkinsonism Relat Disord. 2020 Dec;81:82-83. doi: 10.1016/j.parkreldis.2020.10.011. Epub 2020 Oct 17. Parkinsonism Relat Disord. 2020. PMID: 33096303 No abstract available.
Heterozygous CAPN3 missense variants causing autosomal-dominant calpainopathy in seven unrelated families.
González-Mera L, Ravenscroft G, Cabrera-Serrano M, Ermolova N, Domínguez-González C, Arteche-López A, Soltanzadeh P, Evesson F, Navas C, Mavillard F, Clayton J, Rodrigo P, Servián-Morilla E, Cooper ST, Waddell L, Reardon K, Corbett A, Hernandez-Laín A, Sanchez A, Esteban Perez J, Paradas-Lopez C, Rivas-Infante E, Spencer M, Laing N, Olivé M. González-Mera L, et al. Among authors: dominguez gonzalez c. Neuropathol Appl Neurobiol. 2021 Feb;47(2):283-296. doi: 10.1111/nan.12663. Epub 2020 Sep 28. Neuropathol Appl Neurobiol. 2021. PMID: 32896923
88 results