This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!

Skip to main page content

Add to Collections

Your saved search

Name of saved search:

Search terms:

Test search terms

Would you like email updates of new search results?

Yes
No

Email: (change)

Frequency:

Which day?

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Review

. 1969 Nov;47(5):730-47.

doi: 10.1016/0002-9343(69)90167-3.

The nosology of the mucopolysaccharidoses

PMID: 4242813
DOI: 10.1016/0002-9343(69)90167-3

Review

The nosology of the mucopolysaccharidoses

V A McKusick. Am J Med. 1969 Nov.

. 1969 Nov;47(5):730-47.

doi: 10.1016/0002-9343(69)90167-3.

Author

PMID: 4242813
DOI: 10.1016/0002-9343(69)90167-3

No abstract available

PubMed Disclaimer

Similar articles

The systemic mucopolysaccharidoses.
Spranger J. Spranger J. Ergeb Inn Med Kinderheilkd. 1972;32:165-265. doi: 10.1007/978-3-642-65300-1_4. Ergeb Inn Med Kinderheilkd. 1972. PMID: 4261654 Review. No abstract available.
[Hereditary mucopolysaccharidoses].
Spranger J. Spranger J. Med Klin. 1971 Aug 13;66(23):1105-12. Med Klin. 1971. PMID: 4254502 German. No abstract available.
A new mucopolysaccharidosis.
Horton WA, Schimke RN. Horton WA, et al. J Pediatr. 1970 Aug;77(2):252-8. doi: 10.1016/s0022-3476(70)80332-8. J Pediatr. 1970. PMID: 4988173 No abstract available.
Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy.
McKusick VA, Howell RR, Hussels IE, Neufeld EF, Stevenson RE. McKusick VA, et al. Trans Assoc Am Physicians. 1972;85:151-71. Trans Assoc Am Physicians. 1972. PMID: 4267098 No abstract available.
[Recent data on mucopolysaccharidoses].
Spranger J. Spranger J. Monatsschr Kinderheilkd (1902). 1973 May;121(5):181-3. Monatsschr Kinderheilkd (1902). 1973. PMID: 4268292 Review. German. No abstract available.

See all similar articles

Cited by

Mucopolysacccharidoses: From understanding to treatment, a century of discoveries.
Giugliani R. Giugliani R. Genet Mol Biol. 2012 Dec;35(4 (suppl)):924-31. doi: 10.1590/s1415-47572012000600006. Epub 2012 Dec 18. Genet Mol Biol. 2012. PMID: 23411665 Free PMC article.
Generalized gangliosidosis: acid beta-galactosidase deficiency with early onset, rapid mental deterioration and minimal bone dysplasia.
Fricker H, O'Brien JS, Vassella F, Gugler E, Mühlethaler JP, Spycher M, Wiesmann UN, Herschkowitz N. Fricker H, et al. J Neurol. 1976 Oct 4;213(4):273-81. doi: 10.1007/BF00316267. J Neurol. 1976. PMID: 62026
Arthritis in inherited disorders.
Gupta RC. Gupta RC. Indian J Pediatr. 1973 Sep;40(308):335-41. doi: 10.1007/BF02835157. Indian J Pediatr. 1973. PMID: 4784734 No abstract available.
Profound Impact of Decline in N-Acetylgalactosamine-4-Sulfatase (Arylsulfatase B) on Molecular Pathophysiology and Human Diseases.
Tobacman JK, Bhattacharyya S. Tobacman JK, et al. Int J Mol Sci. 2022 Oct 29;23(21):13146. doi: 10.3390/ijms232113146. Int J Mol Sci. 2022. PMID: 36361933 Free PMC article. Review.
Impaired sulphated glycosaminoglycan metabolism in a patient with GM-2 gangliosidosis (Tay-Sachs disease).
Toma L, Pinto W, Rodrigues VC, Dietrich CP, Nader HB. Toma L, et al. J Inherit Metab Dis. 1990;13(5):721-31. doi: 10.1007/BF01799575. J Inherit Metab Dis. 1990. PMID: 2174089

See all "Cited by" articles

Publication types

Actions

MeSH terms

Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions
Actions

Substances

Actions
Actions
Actions

LinkOut - more resources

Full Text Sources
- Elsevier Science