Publications
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Darling A, Irún P, Giraldo P, Armstrong-Moron J, Gort L, Díaz-Conradi Á, Yubero-Siles D, De Oyarzabal-Sanz AL, Ormazabal-Herrero A, Artuch-Iriberri R, Garcia-Cazorla A and O'Callaghan-Gordo M.
Pediatric Gaucher disease with intermediate type 2-3 phenotype associated with parkinsonian features and levodopa responsiveness
PARKINSONISM & RELATED DISORDERS . 91: 19-22. Number of citations: 5
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Pascual-Alonso A, Martinez-Monseny T, Xiol-Viñas C and Armstrong-Moron J.
MECP2-Related Disorders in Males
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 22(17): 9610. Number of citations: 27
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Trifunov S, Paredes-Fuentes AJ, Badosa-Gallego MC, Codina-Bergadà A, Montoya C, Ruiz-Pesini E, Jou-Munoz C, Garrabou G, Grau-Junyent JM, Yubero-Siles D, Montero-Sanchez R, Muchart-Lopez J, Ortigoza-Escobar JD, O'Callaghan-Gordo M, Nascimento-Osorio A, Català-Temprano A, Garcia-Cazorla A, Jimenez-Mallebrera C and Artuch-Iriberri R.
Circulating Cell-Free Mitochondrial DNA in Cerebrospinal Fluid as a Biomarker for Mitochondrial Diseases
CLINICAL CHEMISTRY . 67(8): 1113-1121. Number of citations: 12
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Sánchez-Espino LF, Ivars M, Vicente-López A, Prat-Torres CS, Armstrong-Moron J and Baselga E.
Erythrokeratodermia Variabilis due to a Compound Heterozygous Variants in the NIPAL4 Gene.
PEDIATRIC DERMATOLOGY . : .