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[Neonatal subcutaneous emphysema].
An Pediatr (Engl Ed). 2019 Apr;90(4):252-253. doi: 10.1016/j.anpedi.2018.03.011. Epub 2018 Oct 15.
An Pediatr (Engl Ed). 2019.
PMID: 29691133
Free article.
Spanish.
No abstract available.
Variant in CACNA1G as a Possible Genetic Modifier of Neonatal Epilepsy in an Infant with a De Novo SCN2A Mutation.
Nieto-Barcelo JJ, Gonzalez Montes N, Gonzalo Alonso I, Martinez F, Aparisi MJ, Martinez-Matilla M, Marco Hernandez AV, Tomás Vila M.
Nieto-Barcelo JJ, et al.
J Pediatr Genet. 2021 Feb 19;12(2):159-162. doi: 10.1055/s-0041-1723958. eCollection 2023 Jun.
J Pediatr Genet. 2021.
PMID: 37090830
Free PMC article.
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[Moyamoya disease: revision and description of a number of pedriatic cases].
Gonzalo-Alonso I, González-Montes NN, Nieto-Barceló JJ, Tomás-Vila M.
Gonzalo-Alonso I, et al. Among authors: nieto barcelo jj.
Rev Neurol. 2021 Oct 16;73(8):261-266. doi: 10.33588/rn.7308.2020624.
Rev Neurol. 2021.
PMID: 34617579
Free article.
Spanish.
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Extending the clinical phenotype of SPTAN1: From DEE5 to migraine, epilepsy, and subependymal heterotopias without intellectual disability.
Marco Hernández AV, Caro A, Montoya Filardi A, Tomás Vila M, Monfort S, Beseler Soto B, Nieto-Barceló JJ, Martínez F.
Marco Hernández AV, et al. Among authors: nieto barcelo jj.
Am J Med Genet A. 2022 Jan;188(1):147-159. doi: 10.1002/ajmg.a.62507. Epub 2021 Sep 30.
Am J Med Genet A. 2022.
PMID: 34590414
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