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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Nat Commun. 2019 Jul 12;10(1):3094. doi: 10.1038/s41467-019-10910-w.
Nat Commun. 2019.
PMID: 31300657
Free PMC article.
Gamma-aminobutyric acid levels in cerebrospinal fluid in neuropaediatric disorders.
Cortès-Saladelafont E, Molero-Luis M, Cuadras D, Casado M, Armstrong-Morón J, Yubero D, Montoya J, Artuch R, García-Cazorla À; Institut De Recerca Sant Joan De Déu Working Group.
Cortès-Saladelafont E, et al. Among authors: armstrong moron j.
Dev Med Child Neurol. 2018 Aug;60(8):780-792. doi: 10.1111/dmcn.13746. Epub 2018 Mar 25.
Dev Med Child Neurol. 2018.
PMID: 29577258
Free article.
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Cataract in You-Hoover-Fong syndrome: TELO2 deficiency.
Del-Prado-Sánchez C, Armstrong-Moron J, Veiga C, Grixolli-Mazzon S, García-Cazorla À, Juliá-Palacios N, Morales-Ballús M.
Del-Prado-Sánchez C, et al. Among authors: armstrong moron j.
Ophthalmic Genet. 2020 Dec;41(6):656-658. doi: 10.1080/13816810.2020.1821382. Epub 2020 Sep 17.
Ophthalmic Genet. 2020.
PMID: 32940098
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[FOXG1, a new gene responsible for the congenital form of Rett syndrome].
Roche-Martinez A, Gerotina E, Armstrong-Moron J, Sans-Capdevila O, Pineda M.
Roche-Martinez A, et al. Among authors: armstrong moron j.
Rev Neurol. 2011 May 16;52(10):597-602.
Rev Neurol. 2011.
PMID: 21488007
Free article.
Spanish.
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Reflex seizures in Rett syndrome.
Roche Martínez A, Alonso Colmenero MI, Gomes Pereira A, Sanmartí Vilaplana FX, Armstrong Morón J, Pineda Marfa M.
Roche Martínez A, et al. Among authors: armstrong moron j.
Epileptic Disord. 2011 Dec;13(4):389-93. doi: 10.1684/epd.2011.0475.
Epileptic Disord. 2011.
PMID: 22258043
Free article.
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Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome.
Barbosa-Gouveia S, Vázquez-Mosquera ME, Gonzalez-Vioque E, Hermida-Ameijeiras Á, Valverde LL, Armstrong-Moron J, Fons-Estupiña MDC, Wintjes LT, Kappen A, Rodenburg RJ, Couce ML.
Barbosa-Gouveia S, et al. Among authors: armstrong moron j.
Int J Mol Sci. 2021 Dec 15;22(24):13484. doi: 10.3390/ijms222413484.
Int J Mol Sci. 2021.
PMID: 34948281
Free PMC article.
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Vanishing white matter disease in a spanish population.
Turón-Viñas E, Pineda M, Cusí V, López-Laso E, Del Pozo RL, Gutiérrez-Solana LG, Moreno DC, Sierra-Córcoles C, Olabarrieta-Hoyos N, Madruga-Garrido M, Aguirre-Rodríguez J, González-Álvarez V, O'Callaghan M, Muchart J, Armstrong-Moron J.
Turón-Viñas E, et al. Among authors: armstrong moron j.
J Cent Nerv Syst Dis. 2014 Jul 13;6:59-68. doi: 10.4137/JCNSD.S13540. eCollection 2014.
J Cent Nerv Syst Dis. 2014.
PMID: 25089094
Free PMC article.
Review.
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