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Page 1
Therapeutic Approaches in Lysosomal Storage Diseases.
Fernández-Pereira C, San Millán-Tejado B, Gallardo-Gómez M, Pérez-Márquez T, Alves-Villar M, Melcón-Crespo C, Fernández-Martín J, Ortolano S. Fernández-Pereira C, et al. Among authors: san millan tejado b. Biomolecules. 2021 Nov 26;11(12):1775. doi: 10.3390/biom11121775. Biomolecules. 2021. PMID: 34944420 Free PMC article. Review.
McArdle disease: 2 case reports.
Diez Morrondo C, Pantoja Zarza L, San Millán Tejado B. Diez Morrondo C, et al. Among authors: san millan tejado b. Reumatol Clin. 2016 May-Jun;12(3):161-3. doi: 10.1016/j.reuma.2015.06.003. Epub 2015 Jul 30. Reumatol Clin. 2016. PMID: 26235145 Free article. English, Spanish.
Systemic Treatment of Fabry Disease Using a Novel AAV9 Vector Expressing α-Galactosidase A.
Biferi MG, Cohen-Tannoudji M, García-Silva A, Souto-Rodríguez O, Viéitez-González I, San-Millán-Tejado B, Fernández-Carrera A, Pérez-Márquez T, Teijeira-Bautista S, Barrera S, Domínguez V, Marais T, González-Fernández Á, Barkats M, Ortolano S. Biferi MG, et al. Among authors: san millan tejado b. Mol Ther Methods Clin Dev. 2020 Oct 22;20:1-17. doi: 10.1016/j.omtm.2020.10.016. eCollection 2021 Mar 12. Mol Ther Methods Clin Dev. 2020. PMID: 33335943 Free PMC article.
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia.
Rodríguez-López C, García-Cárdaba LM, Blázquez A, Serrano-Lorenzo P, Gutiérrez-Gutiérrez G, San Millán-Tejado B, Muelas N, Hernández-Laín A, Vílchez JJ, Gutiérrez-Rivas E, Arenas J, Martín MA, Domínguez-González C. Rodríguez-López C, et al. Among authors: san millan tejado b. J Med Genet. 2020 Sep;57(9):643-646. doi: 10.1136/jmedgenet-2019-106649. Epub 2020 Mar 11. J Med Genet. 2020. PMID: 32161153
[Isolated diplopia as a form of presentation of CADASIL: presentation of a case].
Rodriguez-Pecci MS, de la Fuente-Aguado J, Pato-Pato A, San Millan-Tejado B. Rodriguez-Pecci MS, et al. Among authors: san millan tejado b. Neurologia. 2014 Jan-Feb;29(1):56-9. doi: 10.1016/j.nrl.2012.02.008. Epub 2012 Jun 27. Neurologia. 2014. PMID: 22749569 Free article. Spanish. No abstract available.
Dilated cardiomyopathy and mild limb girdle muscular dystrophy caused by the p.Gly424Ser genetic variant in the fukutin gene.
Larrañaga-Moreira JM, Blanco-Arias P, San Millán-Tejado B, Barge-Caballero G, Crespo-Leiro MG, Barriales-Villa R. Larrañaga-Moreira JM, et al. Among authors: san millan tejado b. Rev Esp Cardiol (Engl Ed). 2021 Nov;74(11):987-989. doi: 10.1016/j.rec.2021.04.015. Epub 2021 Jun 11. Rev Esp Cardiol (Engl Ed). 2021. PMID: 34120883 English, Spanish. No abstract available.