L-iduronidase oor Spaans
L-iduronidase
Vertalings in die woordeboek Engels - Spaans
L-iduronidasa
MPS I is a rare, inherited disease, where the level of-L-iduronidase enzyme activity is much lower than normal
MPS I es una enfermedad hereditaria rara en la que el nivel de actividad de la enzima-L-iduronidasa es mucho menor de lo normal
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voorbeelde
Advanced filtering
Voorbeelde moet herlaai word.
Hurler syndrome, also called MPS I-H, results from a deficiency of α-l-iduronidase.
por la que se fijan modelos de listas de las entidades autorizadas por los Estados miembros con arreglo a lo establecido en diversas disposiciones de la legislación comunitaria en materia veterinaria, así como las normas aplicables a la transmisión de dichas listas a la ComisiónLiterature Literature
Hurler syndrome is due to a deficiency of α-L-iduronidase. 36.
Por favor, síganmeLiterature Literature
MPS I is a rare, inherited disease, where the level of-L-iduronidase enzyme activity is much lower than normal
En la elaboración tradicional sólo se utilizaban tripas naturales de vacunoEMEA0.3 EMEA0.3
Reduced or absent-L-iduronidase activity results in the accumulation of the GAGs, dermatan sulfate and heparan sulfate in many cell types and tissues
No oposición a una concentración notificada (Asunto COMP/M.#- Swiss Life/AWDEMEA0.3 EMEA0.3
Laronidase is a recombinant form of human-L-iduronidase and is produced by recombinant DNA technology using mammalian Chinese Hamster Ovary (CHO) cell culture
Apúrate o se romperá las muñecasEMEA0.3 EMEA0.3
People with MPS I disease have either a low level or no level of an enzyme called-L-iduronidase, which breaks down specific substances (glycosaminoglycans) in the body
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MPS I is a heterogeneous and multisystemic disorder characterised by the deficiency of-L-iduronidase, a lysosomal hydrolase which catalyses the hydrolysis of terminal-L-iduronic residues of dermatan sulfate and heparan sulfate
Ya está.- ¡ Haga algo, muchacho!EMEA0.3 EMEA0.3
Aldurazyme is indicated for long-term enzyme replacement therapy in patients with a confirmed diagnosis of Mucopolysaccharidosis I (MPS I;-L-iduronidase deficiency) to treat the non-neurological manifestations of the disease (see section
Lamento llegar tarde.- ¿ Dónde has estado?EMEA0.3 EMEA0.3
Aldurazyme is used for enzyme replacement therapy in patients with a confirmed diagnosis of mucopolysaccharidosis I (MPS I;-L-iduronidase deficiency) to treat the non-neurological symptoms of the disease (not connected with the brain or nerves
Un momento, HenryEMEA0.3 EMEA0.3
For functional analysis of alpha-L-iduronidase Substrates, see our complete listing of alpha-L-iduronidase Antibodies.
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People with Scheie syndrome are missing an enzyme called lysosomal alpha-L-iduronidase.
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The activity of the intralysosomal L‐iduronidase enzyme from peripheral blood leukocytes was assessed as deficient.
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People with Scheie syndrome are missing an enzyme called lysosomal alpha-L-iduronidase.
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People with MPS I do not make an enzyme called lysosomal alpha-L-iduronidase.
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EKG Genetic testing for changes to the alpha-L-iduronidase (IDUA) gene
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It is caused by a deiciency in alpha-L-iduronidase.
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Causes People with Hurler syndrome do not make an enzyme called lysosomal alpha-L-iduronidase.
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Genetic testing for changes to the alpha-L-iduronidase (IDUA) gene
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Enzyme replacement therapy for patients with a defect in the enzyme a-L-iduronidase is now possible.
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EKG Genetic testing for changes to the alpha-L-iduronidase (IDUA) gene
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People with Hurler syndrome do not make an enzyme called lysosomal alpha-L-iduronidase.
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Genetic testing for the alpha-L-iduronidase (IDUA) gene
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One of these enzymes is called alpha-L-iduronidase (IDUA).
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MPS I disease is an inherited genetic disorder caused by a deficiency in an enzyme called alpha-L-iduronidase.
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It is an inherited genetic disorder of metabolism in which individual's body is unable to make an enzyme alpha-L-iduronidase, responsible for metabolic breakdown of mucopolysaccharides.
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29 sinne gevind in 12 ms. Hulle kom uit baie bronne en word nie nagegaan nie.