Evolución de paciente con mucopolisacaridosis tipo II que inició con idursulfasa a los tres años de edad
Author:
Publisher
GRAPHIMEDIC SA DE CV
Subject
Pediatrics, Perinatology and Child Health
Reference21 articles.
1. Brusius-Facchin AC, Schwartz IVD, Zimmer C, Ribeiro MG, Acosta AX, Horovitz D, et al. Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients. Mol Genet Metab. 2014; 111 (2): 133-138.
2. Guffon N, Heron B, Chabrol B, Feillet F, Montauban V, Valayannopoulos V. Diagnosis, quality of life, and treatment of patients with Hunter syndrome in the French healthcare system: a retrospective observational study. Orphanet J Rare Dis. 2015; 10 (1): 1-13.
3. Stapleton M, Kubaski F, Mason RW, Yabe H, Suzuki Y, Orii KE et al. Presentation and treatments for mucopolysaccharidosis type II. Expert Opin Orphan Drugs. 2017; 5 (4): 295-307.
4. Acosta-gualandri A. Mucopolisacaridosis II: nueva mutación patogénica en gen IDS. Acta Med Costarric. 2014; 56 (4): 180-182.
5. Mendoza-Ruvalcaba SDC, Brambila-Tapia AJL, Juárez-Osuna JA, Da Silva-José TD, García-Ortiz JE. Biochemical diagnosis of mucopolysaccharidosis in a Mexican reference center. Genet Mol Biol. 2020; 43 (1): 1-5.
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