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Abbreviation: MPS I
Appearance Frequency: 365 time(s)
Long forms: 5

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
Mucopolysaccharidosis type I
(358 times)
Molecular Biology
(77 times)
IDUA (143 times)
ERT (63 times)
GAG (47 times)
1984 Antenatal diagnosis of mucopolysaccharidosis type I (Hurler's disease) is not possible by electron microscopy of uncultured amniotic fluid cells.
MPS type I
(3 times)
Genetics, Medical
(1 time)
ERT (2 times)
MPS (2 times)
AXIN1 (1 time)
2005 Changes in hair morphology of mucopolysaccharidosis I patients treated with recombinant human alpha-L-iduronidase (laronidase, Aldurazyme).
MPS IH, or Hurler syndrome
(2 times)
Pediatrics
(1 time)
AHI (1 time)
GAGs (1 time)
HSCT (1 time)
2018 Neurobehavioral phenotypes of neuronopathic mucopolysaccharidoses.
marrow transplanted girl with Hurler
(1 time)
Neurology
(1 time)
CSF (1 time)
GVHD (1 time)
2009 Late cerebral graft versus host reaction in a bone marrow transplanted girl with Hurler (MPS I) disease.
MPS IATT
(1 time)
Neurology
(1 time)
CC (1 time)
WM (1 time)
2019 Attention and corpus callosum volumes in individuals with mucopolysaccharidosis type I.