Hurlers or "mps i" or mucopolysaccharidoses Treff i utvalgte kilder: [Skjul boksen]
  1. Frambu
    -
    www.frambu.no/hurlers-sykdom
    /
    Hurlers sykdom (mukopolysakkaridose type I, MPS I, MPS IH) er en arvelig, medfødt stoffskiftesykdom som skyldes mangelfull nedbrytning av mukopolysakkaridene dermatansulfat og heparansulfat, med derav følgende opphopning og ...
  2. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-gb/215/history-exam
    /
    ... OSA or who snore is common. hx of mucopolysaccharidoses Commonly associated with OSA. hx of GORD Commonly ... nlm.nih.gov/pubmed/14746382?tool=bestpractice.com mucopolysaccharidoses Has been associated with increased risk of OSA. [ ...
  3. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-us/215/history-exam
    /
    ... OSA or who snore is common. hx of mucopolysaccharidoses Commonly associated with OSA. hx of GERD Commonly ... nlm.nih.gov/pubmed/14746382?tool=bestpractice.com mucopolysaccharidoses Has been associated with increased risk of OSA. [ ...
  4. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-gb/1021/treatment-algorithm
    /
    ... ALL patients in selected patient group Primary options MPS I laronidase open_in_new : children >5 years of ... replacement therapy (ERT) is of established benefit in MPS I, II, IVA (Morquio A syndrome), and VI; [90] ...
  5. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-us/1021/treatment-algorithm
    /
    ... ALL patients in selected patient group Primary options MPS I laronidase open_in_new : children >5 years of ... replacement therapy (ERT) is of established benefit in MPS I, II, IVA (Morquio A syndrome), and VI; [97] ...
  6. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-gb/438/history-exam
    /
    ... 6th ed. Philadelphia, PA: Mosby/Elsevier, 2006:1151. mucopolysaccharidoses Umbilical hernias are found in the familial lysosomal storage disease, Hurler's syndrome. [9] Hulsebos RG, Zeebregts CJ, de ...
  7. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-us/438/history-exam
    /
    ... 6th ed. Philadelphia, PA: Mosby/Elsevier, 2006:1151. mucopolysaccharidoses Umbilical hernias are found in the familial lysosomal storage disease, Hurler syndrome. [9] Hulsebos RG, Zeebregts CJ, de Langen ...
  8. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-gb/1021/pdf/1021.pdf
    /
    ... deficiency) • GM1 gangliosidosis (beta-galactosidase deficiency). Mucopolysaccharidosis (MPS) • MPS I (alpha-L-iduronidase deficiency) severe form (Hurler's), ...
  9. bmj-bestpractice
    -
    https://bestpractice.bmj.com/topics/en-us/1021/pdf/1021.pdf
    /
    ... deficiency) • GM1 gangliosidosis (beta galactosidase deficiency). Mucopolysaccharidosis (MPS) • MPS I (alpha-L-iduronidase deficiency) severe form (Hurler), milder ...
  10. Frambu
    -
    www.frambu.no/diagnoser
    /
    ... hemiplegi L1 syndrom Möbius' syndrom Cohens syndrom Pseudo-Hurler polydystrofi MPS-sykdommer ANCL Maternally inherited diabetes and ... Muskeldystrofi, medfødt CDG Spinal muskelatrofi INAD Trippel X Hurlers sykdom (MPS I) Seninfantil nevronal ceroid lipofuscinose Dystrofia ...
første · forrige · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · neste · siste