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Page 1
Familial partial lipodystrophy syndromes.
Fernández-Pombo A, Sánchez-Iglesias S, Cobelo-Gómez S, Hermida-Ameijeiras Á, Araújo-Vilar D. Fernández-Pombo A, et al. Among authors: hermida ameijeiras a. Presse Med. 2021 Nov;50(3):104071. doi: 10.1016/j.lpm.2021.104071. Epub 2021 Oct 2. Presse Med. 2021. PMID: 34610417 Review.
Celia's Encephalopathy (BSCL2-Gene-Related): Current Understanding.
Sánchez-Iglesias S, Fernández-Pombo A, Cobelo-Gómez S, Hermida-Ameijeiras Á, Alarcón-Martínez H, Domingo-Jiménez R, Ruíz Riquelme AI, Requena JR, Araújo-Vilar D. Sánchez-Iglesias S, et al. Among authors: hermida ameijeiras a. J Clin Med. 2021 Apr 1;10(7):1435. doi: 10.3390/jcm10071435. J Clin Med. 2021. PMID: 33916074 Free PMC article. Review.
Is there new hope for rare diseases?
Hermida Ameijeiras Á. Hermida Ameijeiras Á. Med Clin (Barc). 2025 Jun 27;164(12):106949. doi: 10.1016/j.medcli.2025.106949. Epub 2025 Apr 28. Med Clin (Barc). 2025. PMID: 40300526 English, Spanish. No abstract available.
Current status of the immunogenicity of enzyme replacement therapy in fabry disease.
Gómez-Cerezo JF, Fernández-Martín J, Barba-Romero MÁ, Sánchez-Martínez R, Hermida-Ameijeiras A, Camprodon-Gómez M, Ortolano S, Lopez-Rodriguez MA. Gómez-Cerezo JF, et al. Among authors: hermida ameijeiras a. Orphanet J Rare Dis. 2025 May 26;20(1):253. doi: 10.1186/s13023-025-03705-4. Orphanet J Rare Dis. 2025. PMID: 40420145 Free PMC article. Review.
Disrupted synaptic gene expression in Fabry disease: Findings from RNA sequencing.
López-Valverde L, Vázquez-Mosquera ME, Colón-Mejeras C, Álvarez JV, López-Pardo BM, López LL, Sánchez-Martínez R, López-Mendoza M, López-Rodríguez M, Villacorta-Argüelles E, Goicoechea-Diezhandino MA, Guerrero-Márquez FJ, Ortolano S, Leao-Teles E, Hermida-Ameijeiras Á, Couce ML. López-Valverde L, et al. Among authors: hermida ameijeiras a. Neurobiol Dis. 2025 Jun 1;209:106908. doi: 10.1016/j.nbd.2025.106908. Epub 2025 Apr 13. Neurobiol Dis. 2025. PMID: 40233852 Free article.
54 results