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Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain.
Genes (Basel). 2024 Apr 28;15(5):568. doi: 10.3390/genes15050568.
Genes (Basel). 2024.
PMID: 38790198
Free PMC article.
Expanding the phenotype of PIGP deficiency to multiple congenital anomalies-hypotonia-seizures syndrome.
Martín-Grau C, Orellana Alonso C, Roselló Piera M, Pedrola Vidal L, Llorens-Salvador R, Quiroga R, Marín Reina P, Rubio Moll JS, Gómez Portero R, Martínez-Castellano F.
Martín-Grau C, et al. Among authors: pedrola vidal l.
Clin Genet. 2023 Aug;104(2):245-250. doi: 10.1111/cge.14340. Epub 2023 May 1.
Clin Genet. 2023.
PMID: 37125481
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Facial onset sensory and motor neuronopathy: a motor neuron disease with an oligogenic origin?
Vázquez-Costa JF, Pedrola Vidal L, Moreau-Le Lan S, Teresí-Copoví I, Frasquet M, Chumillas MJ, Sevilla T.
Vázquez-Costa JF, et al. Among authors: pedrola vidal l.
Amyotroph Lateral Scler Frontotemporal Degener. 2019 May;20(3-4):172-175. doi: 10.1080/21678421.2019.1582671. Epub 2019 Mar 20.
Amyotroph Lateral Scler Frontotemporal Degener. 2019.
PMID: 30889971
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Delayed Presentation and Prolonged Survival of a Child with Surfactant Protein B Deficiency.
López-Andreu JA, Hidalgo-Santos AD, Fuentes-Castelló MA, Mancheño-Franch N, Cerón-Pérez JA, Esteban-Ricós MJ, Pedrola-Vidal L, Nogee LM.
López-Andreu JA, et al. Among authors: pedrola vidal l.
J Pediatr. 2017 Nov;190:268-270.e1. doi: 10.1016/j.jpeds.2017.07.009. Epub 2017 Sep 6.
J Pediatr. 2017.
PMID: 28888561
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