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14 results
  1. ... C. B., “A Chemical Method for the Antenatal Diagnosis of Mucopolysaccharidoses." Lancet, 1, 83 (1970). 26c) Nadlec, H. L., ...
  2. ... C. B., “A Chemical Method for the Antenatal Diagnosis of Mucopolysaccharidoses." Lancet, 1, 83 (1970). 26c) Nadlec, H. L., ...
  3. NLM Digital Collections - MEDLARS indexing : integrated authority file 
    Publication: [Bethesda, Md.] : National Library of Medicine, Bibliographic Services Division, 1968
    ... Eponymous Syndromes and Diseases) Index LIPOCHONDRODY: .ROPHY (68) mucopolysaccharidosis II syn. Hunter's syndrome similar to u;ucopolysaccharidosis I except there is absence of gibbus and symptoms are generally milder. Retinitis pigmentosa, nodular skin lesions, ...
  4. NLM Digital Collections - Rare diseases. Although limited, available evidence suggests medical and other costs can be ... 
    Publication: Washington, DC : United States Government Accountability Office, October 2021
    ... the Diagnostic Delay in Two Ultra-Orphan Diseases (Mucopolysaccharidosis Types ... time from first symptom to confirmed diagnoses was 4 years, ranging to ...
  5. 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
    ... Metabolism QV 38 Military supplies UH 420-425 Mucopolysaccharidosis IV WD 205.5.C2 Packaging QV 825 ... Arterial Bypass see Cerebral Revascularization Eccentro-Osteochondrodysplasia see Mucopolysaccharidosis IV Eccrine Glands WR 400 ALWAYS CONSULT MAIN ...
  6. ... Metabolism QV 38 Military supplies UH 420-425 Mucopolysaccharidosis IV WD 205.5.C2 Packaging QV 825 ... Arterial Bypass see Cerebral Revascularization Eccentro-Osteochondrodysplasia see Mucopolysaccharidosis IV Eccrine Glands WR 400 ALWAYS CONSULT MAIN ...
  7. NLM Digital Collections - On Lumpers and Splitters, or the Nosology of Genetic Disease 
    Publication: The National Foundation-March of Dimes, January 1969
    ... the focus, eg in studies of the genetic mucopolysaccharidoses and the separation of homocystinuria from the Marfan ... of urinary excretion of mucopoly- saccharides in the mucopolysaccharidoses helps disting- uish several types,2 eg types ...
  8. NLM Digital Collections - Integrated authority file : IAF 
    Publication: [Bethesda, Md.] : U.S. Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health, 1974
    ... marmot X SQUIRRELS Maroteaux-Lamy syndrome (1) X MUCOPOLYSACCHARIDOSIS X CKONDROlTIN/metabolisa p SYNDROKE Maroteaux-Laay syndroae ( ... see Phlebotomus fever virus Sanfilippo's syndrome (SYN) X MUCOPOLYSACCHARIDOSIS X BENTAL RETARDATION P SYNDROHE Sango fever (HSH) ...
  9. NLM Digital Collections - Quality of healthcare 
    Publication: [Toronto, Ontario] : Thomson Reuters, 20-December-2021
    ... of Glycogen Storage Disease Type II (Pompe Disease), Mucopolysaccharidosis Type 1 (MPS1), and X-linked Adrenoleukodystrophy (XALD) ... covered health care services and benefits for the diagnosis, prevention, and treatment of mental, emotional, and nervous ...
  10. NLM Digital Collections - Annual report - National Eye Institute (1980) 
    Publication: [Bethesda, Md.] : National Eye Institute
    ... been shown that patients with some types of mucopolysaccharidoses have RP. The levels and kinds of glycosaminoglycans ( ... guinea pigs sensitized with disc membranes developed clinical symptoms of EAU between 3 and 6 weeks. Histologically, ...
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