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searching for Mucopolysaccharidosis type I 13 found (24 total)

alternate case: mucopolysaccharidosis type I

Coarse facial features (406 words) [view diff] exact match in snippet view article find links to article

Sly syndrome Mucopolysaccharidosis type I Hurler syndrome Mucopolysaccharidosis type I Hurler/Scheie syndrome Mucopolysaccharidosis type I Scheie syndrome
BioMarin Pharmaceutical (1,658 words) [view diff] exact match in snippet view article find links to article
BioMarin was the first company to provide therapeutics for mucopolysaccharidosis type I (MPS I), by manufacturing laronidase (Aldurazyme, commercialized
David Sillence (471 words) [view diff] exact match in snippet view article find links to article
Constitutional Disorders of the Skeletal, the International Mucopolysaccharidosis type I expert committee, the National Fabry Disease and MPS expert committees
List of diseases (M) (2,463 words) [view diff] exact match in snippet view article
Mucopolysaccharidosis type 4 Mucopolysaccharidosis type I Hurler syndrome Mucopolysaccharidosis type I Hurler/Scheie syndrome Mucopolysaccharidosis type I Scheie syndrome
Haematopoietic system (1,162 words) [view diff] case mismatch in snippet view article find links to article
KK, Wijburg FA (March 2016). "Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation"
Iduronidase (2,088 words) [view diff] exact match in snippet view article find links to article
"Mucopolysaccharidosis Type I". GeneReviews. Seattle (WA): University of Washington. ISSN 2372-0697. PMID 20301341.</ref> "Mucopolysaccharidosis type I"
Macroglossia (1,042 words) [view diff] exact match in snippet view article find links to article
doi:10.1007/s00247-008-0941-7. PMID 18685841. S2CID 22012119. "Mucopolysaccharidosis type I". http://moon.ouhsc.edu/kfung/jty1/neurohelp/ZNN0IE23.htm "Omim
Restrictive cardiomyopathy (1,269 words) [view diff] exact match in snippet view article find links to article
disease Hereditary hemochromatosis Glycogen storage disease Mucopolysaccharidosis type I (Hurler syndrome) Mucopolysaccharidosis type II (Hunter syndrome)
Osteochondrodysplasia (1,815 words) [view diff] exact match in snippet view article find links to article
replacement therapy with laronidase (Aldurazyme®) for treating mucopolysaccharidosis type I". Cochrane Database of Systematic Reviews. 6: CD009354. doi:10
List of skin conditions (17,721 words) [view diff] exact match in snippet view article find links to article
syndrome Hurler syndrome (gargoylism, mucopolysaccharidosis type I) Hurler–Scheie syndrome (mucopolysaccharidosis type I H-S) Hyaluronidase deficiency (mucopolysaccharidosis
Hematopoietic stem cell (4,077 words) [view diff] case mismatch in snippet view article find links to article
Mercer J, et al. (March 2016). "Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation"
Hematopoietic stem cell transplantation (7,488 words) [view diff] case mismatch in snippet view article find links to article
Mercer J, et al. (March 2016). "Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation"
Maria Luisa Escolar (3,407 words) [view diff] exact match in snippet view article find links to article
impairment, cognitive function, and motor skills in children with mucopolysaccharidosis type I (Hurler syndrome); adaptive behavior and cognitive, language