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

Year Number of Results
2012 1
2013 2
2014 2
2015 4
2016 6
2017 4
2018 2
2019 8
2020 8
2021 8
2022 0
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39 results
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Page 1
[Advances in the treatment of Duchenne muscular dystrophy].
Ortez C, Natera de Benito D, Carrera García L, Expósito J, Nolasco G, Nascimento A. Ortez C, et al. Among authors: natera de benito d. Medicina (B Aires). 2019;79 Suppl 3:77-81. Medicina (B Aires). 2019. PMID: 31603849 Free article. Review. Spanish.
COVID-19 in children with neuromuscular disorders.
Natera-de Benito D, Aguilera-Albesa S, Costa-Comellas L, García-Romero M, Miranda-Herrero MC, Rúbies Olives J, García-Campos Ó, Martínez Del Val E, Martinez Garcia MJ, Medina Martínez I, Cancho-Candela R, Fernandez-Garcia MA, Pascual-Pascual SI, Gómez-Andrés D, Nascimento A; Neuromuscular Working Group of Spanish Pediatric Neurology Society. Natera-de Benito D, et al. J Neurol. 2021 Sep;268(9):3081-3085. doi: 10.1007/s00415-020-10339-y. Epub 2021 Jan 2. J Neurol. 2021. PMID: 33387010 Free PMC article.
Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain.
Gonzalez-Quereda L, Rodriguez MJ, Diaz-Manera J, Alonso-Perez J, Gallardo E, Nascimento A, Ortez C, Natera-de Benito D, Olive M, Gonzalez-Mera L, Munain AL, Zulaica M, Poza JJ, Jerico I, Torne L, Riera P, Milisenda J, Sanchez A, Garrabou G, Llano I, Madruga-Garrido M, Gallano P. Gonzalez-Quereda L, et al. Among authors: natera de benito d. Genes (Basel). 2020 May 11;11(5):539. doi: 10.3390/genes11050539. Genes (Basel). 2020. PMID: 32403337 Free PMC article.
[Diagnosis and treatment of congenital myopaties].
Natera de Benito D, Ortez C, Carrera García L, Expósito J, Bobadilla E, Nascimento A. Natera de Benito D, et al. Medicina (B Aires). 2019;79 Suppl 3:82-86. Medicina (B Aires). 2019. PMID: 31603850 Free article. Review. Spanish.
[Current status of congenital myasthenic syndromes].
Bestue-Cardiel M, Natera-de Benito D. Bestue-Cardiel M, et al. Among authors: natera de benito d. Rev Neurol. 2017 Aug 16;65(4):161-176. Rev Neurol. 2017. PMID: 28726234 Free article. Review. Spanish.
Description of Restrictively Defined Acute Flaccid Myelitis.
Berciano J, Natera-de Benito D. Berciano J, et al. Among authors: natera de benito d. JAMA Pediatr. 2019 Jul 1;173(7):701-702. doi: 10.1001/jamapediatrics.2019.1266. JAMA Pediatr. 2019. PMID: 31135824 No abstract available.
[Neurofibromatosis type 2 in childhood: a clinical characterization].
Hinojosa-Mateo CM, Reche-Sainz JA, Hernandez-Nunez A, Ramos-Lopez M, Arpa-Fernandez A, Natera-de Benito D. Hinojosa-Mateo CM, et al. Among authors: natera de benito d. Rev Neurol. 2017 Feb 1;64(3):119-124. Rev Neurol. 2017. PMID: 28128429 Free article. Review. Spanish.
CHRNG-related nonlethal multiple pterygium syndrome: Muscle imaging pattern and clinical, histopathological, and molecular genetic findings.
Carrera-García L, Natera-de Benito D, Dieterich K, de la Banda MGG, Felter A, Inarejos E, Codina A, Jou C, Roldan M, Palau F, Hoenicka J, Pijuan J, Ortez C, Expósito-Escudero J, Durand C, Nugues F, Jimenez-Mallebrera C, Colomer J, Carlier RY, Lochmüller H, Quijano-Roy S, Nascimento A. Carrera-García L, et al. Among authors: natera de benito d. Am J Med Genet A. 2019 Jun;179(6):915-926. doi: 10.1002/ajmg.a.61122. Epub 2019 Mar 14. Am J Med Genet A. 2019. PMID: 30868735 Review.
Epilepsy in LAMA2-related muscular dystrophy: An electro-clinico-radiological characterization.
Natera-de Benito D, Muchart J, Itzep D, Ortez C, González-Quereda L, Gallano P, Ramirez A, Aparicio J, Domínguez-Carral J, Carrera-García L, Expósito-Escudero J, Pardo Cardozo N, Cuadras D, Codina A, Jou C, Jimenez-Mallebrera C, Palau F, Colomer J, Arzimanoglou A, Nascimento A, San Antonio-Arce V. Natera-de Benito D, et al. Epilepsia. 2020 May;61(5):971-983. doi: 10.1111/epi.16493. Epub 2020 Apr 8. Epilepsia. 2020. PMID: 32266982
39 results