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Gargolismo o síndrome de Hurler
(Sociedad Chilena de Pediatría, 1950)
Mucopolisacaridosis de tipo I Hurler: Informe de un caso
(Sociedad Argentina de Pediatría (SAP), 2014-03-05)
Mucopolysaccharidosis I (MPS I) is a rare, recessively inherited, lysosomal storage disorder caused by deficiency on the enzyme α-L-iduronidase. This defect results in accumulation of heparan and dermatan sulfate in different ...
Síndrome de Hurler asociado a alcaptonuria : estudio bioquímico de un caso
(Universidad Veracruzana, 2009)
MUCOPOLISACARIDOSIS TYPE I: HURLER SYNDROME ABOUT A CASEMUCOPOLISACARIDOSIS TIPO I: SÍNDROME DE HURLER A PROPÓSITO DE UN CASO
(Instituto Médico "Sucre", 2019)
Variables Epidemiológicas de la Mucopolisacaridosis en el Cantón Archidona, Hospital José María Velasco Ibarra, Período 2017-2018
(Escuela Superior Politécnica de Chimborazo, 2019-10-10)
This study aimed to characterize the epidemiological variables of mucopolysaccharidosis in Archidona canton, Napo province, in the 2017-2018 period. The type of research applied was descriptive, retrospective, cross-sectional, ...
Terapia de reposição da enzima alfa-L-iduronidase recombinante em pacientes portadores de mucopolissacaridose do tipo I: análise de glicosaminoglicanos urinários e correlações clínicas
(Universidade Federal de São Paulo (UNIFESP), 2009)
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disease caused by deficiency of -L-iduronidase, which cleaves terminal iduronic acid residues of glycosaminoglycans (GAGs), heparan sulphate (HS) and dermatan ...