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Val50Met hereditary transthyretin amyloidosis: not just a medical problem, but a psychosocial burden.
Orphanet J Rare Dis. 2021 Jun 10;16(1):266. doi: 10.1186/s13023-021-01910-5.
Orphanet J Rare Dis. 2021.
PMID: 34112225
Free PMC article.
Phenotypic Expression and Outcomes in Patients with the p.Arg301Gln GLA Variant in Anderson-Fabry Disease.
Blanco R, Rico-Ramírez Y, Hermida-Ameijeiras Á, Abdullah IMS, Lau K, Alvarez-Rubio J, Fortuny E, Martínez-Monzonís A, Nowak A, Nordbeck P, Veras-Burgos C, Pons-Llinares J, Rossi E, Caimi-Martínez F, Bosch-Rovira T, Alamar-Cervera M, Ruiz-Pizarro V, Torres-Juan L, Heine-Suñer D, Ripoll-Vera T.
Blanco R, et al. Among authors: bosch rovira t.
Int J Mol Sci. 2024 Apr 12;25(8):4299. doi: 10.3390/ijms25084299.
Int J Mol Sci. 2024.
PMID: 38673884
Free PMC article.
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[Rhabdomyolysis associated with combined treatment of cerivastatin and gemfibrozil].
Bosch Rovira T, Llompart Pou JA, Forteza-Rey J.
Bosch Rovira T, et al.
Rev Clin Esp. 2001 Dec;201(12):731-2. doi: 10.1016/s0014-2565(01)70966-6.
Rev Clin Esp. 2001.
PMID: 11835892
Spanish.
No abstract available.
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