- NLM Digital Collections - MEDLARS indexing : integrated authority filePublication: [Bethesda, Md.] : National Library of Medicine, Bibliographic Services Division, 1968... sand-puppy Index RODENTS (68) Sanfilippo's syndrome see mucopolysaccharidosis III Sango fever see EPIDEMIC HEMORRHAGIC FEVER sanitaire (Fre) tmedical, public healths SANITARY ENGINEERING ★analysis - invalid ★prevention 6c control - invalid SANITATION ★analysis -invalid ★prevention 6c ...
- NLM Digital Collections - National Library of Medicine classification : a scheme for the shelf arrangement of library ...Publication: Bethesda, Md. : U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Library of Medicine ; Washington, D.C. : For sale by the Supt. of Docs., U.S. G.P.O., 1994... 100 Nutrition surveys QU 146 Physiology WI 102 Prevention WA 695 Huntington Chorea see Huntington's Disease Huntington's Disease WL 390 Hurler-Scheie Syndrome see Mucopolysaccharidosis I Hurler's Syndrome see Mucopolysaccharidosis I Hurricanes see ...
- NLM Digital Collections - Beikoku Kokuritsu Igaku Toshokan bunruihō : igaku oyobi kanren bun'ya ni okeru tosho haikahōPublication: Tōkyō : Nihon Igaku Toshokan Kyōkai, 1996... 100 Nutrition surveys QU 146 Physiology WI 102 Prevention WA 695 Huntington Chorea see Huntington's Disease Huntington s Disease WL 390 Hurler-Scheie Syndrome see Mucopolysaccharidosis I Hurler s Syndrome see Mucopolysaccharidosis I Hurricanes see ...
- ... lysosome, the appropriate intracellular site [ Russell & Clarke ... & Muenzer 2001 ]. The following are important considerations: ...
- ... published></health-condition-summary><health-condition-summary ><name >Mucopolysaccharidosis type I</name><ghr-page >https://medlineplus.gov/genetics/condition/mucopolysaccharidosis-type-i</ghr-page><text-list ><text ><text- ...
- ... type C , Wolman disease (lysosomal lipase deficiency), the mucopolysaccharidoses (including mucopolysaccharidosis type I and mucopolysaccharidosis type II ), ...
- ... ethnicity, individuals have typical Hurler-like facies (see Mucopolysaccharidosis Type 1 ) or coarse facial features, macrocephaly with ... overlap with other lysosomal storage diseases (e.g., mucopolysaccharidosis type 1 ). However, the distinctive clinical features associated ...
- ... or cat cry syndrome/ or down syndrome/ or mucopolysaccharidosis/ or phenylketonuria/ or pyruvate dehydrogenase/ or rubinstein syndrome/ ... lesch-nyhan syndrome/ or fragile x syndrome/ or mucopolysaccharidoses/ or exp phenylketonurias/ or exp prader-willi syndrome/ ...
- ... January 28, 2005; Last Update: July 30, 2015. Mucopolysaccharidosis Type I Lorne A Clarke. Initial Posting: October 31, 2002; Last Update: February 11, 2016. Mucopolysaccharidosis Type II Maurizio Scarpa. Initial Posting: November 6, ...
- ... or cat cry syndrome/ or down syndrome/ or mucopolysaccharidosis/ or phenylketonuria/ or pyruvate dehydrogenase/ or rubinstein syndrome/ ... lesch-nyhan syndrome/ or fragile x syndrome/ or mucopolysaccharidoses/ or exp phenylketonurias/ or exp prader-willi syndrome/ ...
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