Read: MPs have a responsibility to the people, not their political parties.
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Everyone knows that MPs from the governing parties will support government legislation.
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MPs later vote to extend the detention time limit to 28 days.
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However, many MPs from across the political spectrum shared the Speaker's view.
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Corbyn is under increasing pressure from MPs to support a second referendum.
1
These recommendations will help to obtain a complete and correct diagnosis of mucopolysaccharidosis, rendering also possible genetic counseling.
2
Background: Recent reports have shown a correlation between extensive Mongolian spots and mucopolysaccharidosis type II (Hunter syndrome).
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Cumulatively, our results allow transition to pre-clinical studies of SB-mediated alpha-L-iduronidase expression and correction of mucopolysaccharidosis type I in animal models.
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Hunter syndrome (mucopolysaccharidosis type II) is a rare and life-limiting multisystemic disorder with an X-linked recessive pattern of inheritance.
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Renal failure was diagnosed in an 11-mo-old male domestic shorthair cat from a colony with mucopolysaccharidosis type I lysosomal storage disease.
Ús de mucopolysaccharidoses en anglès
1
Cardiac involvement has been reported in various mucopolysaccharidoses syndromes.
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The mucopolysaccharidoses are a group of lysosomal storage disorders caused by defects in the degradation of glycosaminoglycans.
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Pain is a common feature in mucopolysaccharidoses.
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This case highlights the importance of early routine cardiac screening for conduction abnormalities and close follow-up in patients with mucopolysaccharidoses syndromes.
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Almost all known human sphingolipidoses, two mucopolysaccharidoses and aspartylglycosaminuria have so far been duplicated in mice and more are expected in the near future.
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Mucopolysaccharidoses are a family of metabolic disorders characterized by a deficiency in the catabolic lysosomal pathways.