Mucopolysaccharide storage disease in three fami... [Pediatr Res. 1979] - PubMed

Save items

loading

Related citations in PubMed

An improved method for heterozygote identification in feline and human mucopolysaccharidosis VI, arylsulfatase-B deficiency. [Enzyme. 1981]
An improved method for heterozygote identification in feline and human mucopolysaccharidosis VI, arylsulfatase-B deficiency.
McGovern MM, Vine DT, Haskins ME, Desnick RJ. Enzyme. 1981; 26(4):206-10.
Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome. [Science. 1977]
Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome.
Jezyk PF, Haskins ME, Patterson DF, Mellman WJ, Greenstein M. Science. 1977 Nov 25; 198(4319):834-6.
Morphology of leukocytes from cats affected with alpha-mannosidosis and mucopolysaccharidosis VI (MPS VI). [Vet Pathol. 1989]
Morphology of leukocytes from cats affected with alpha-mannosidosis and mucopolysaccharidosis VI (MPS VI).
Alroy J, Freden GO, Goyal V, Raghavan SS, Schunk KL. Vet Pathol. 1989 Jul; 26(4):294-302.
Review [Arylsulfatase deficiency and various metabolic diseases]. [Pediatr Pol. 1978]
Review [Arylsulfatase deficiency and various metabolic diseases].
Czyzewska K, Działoszyński L. Pediatr Pol. 1978 Sep; 53(9):1129-35.
Review Enzymic diagnosis of the genetic mucopolysaccharide storage disorders. [Methods Enzymol. 1978]
Review Enzymic diagnosis of the genetic mucopolysaccharide storage disorders.
Hall CW, Liebaers I, Di Natale P, Neufeld EF. Methods Enzymol. 1978; 50:439-56.

See reviews... See all...

Cited by 11 PubMed Central articles

Long-term amelioration of feline Mucopolysaccharidosis VI after AAV-mediated liver gene transfer. [Mol Ther. 2011]
Long-term amelioration of feline Mucopolysaccharidosis VI after AAV-mediated liver gene transfer.
Cotugno G, Annunziata P, Tessitore A, O'Malley T, Capalbo A, Faella A, Bartolomeo R, O'Donnell P, Wang P, Russo F, et al. Mol Ther. 2011 Mar; 19(3):461-9. Epub 2010 Nov 30.
Review Gene therapy for lysosomal storage diseases (LSDs) in large animal models. [ILAR J. 2009]
Review Gene therapy for lysosomal storage diseases (LSDs) in large animal models.
Haskins M. ILAR J. 2009; 50(2):112-21.
Review Animal models for mucopolysaccharidosis disorders and their clinical relevance. [Acta Paediatr Suppl. 2007]
Review Animal models for mucopolysaccharidosis disorders and their clinical relevance.
Haskins ME. Acta Paediatr Suppl. 2007 Apr; 96(455):56-62.

See all...

Related information

Related Citations
Calculated set of PubMed citations closely related to the selected article(s) retrieved using a word weight algorithm. Related articles are displayed in ranked order from most to least relevant, with the “linked from” citation displayed first.
Gene (OMIM)
Gene records associated with Online Mendelian Inheritance in Man (OMIM) records that cite the current articles in their reference lists.
Nucleotide (Weighted)
Nucleotide records associated with the current articles through the Gene database. These are the related sequences on the Gene record that are added manually by NCBI.
OMIA
Online Mendelian Inheritance in Animals (OMIA) records that cite the current articles.
OMIM (calculated)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as references in the light bulb links within or in the citations at the end of the OMIM record. The references available through the light bulb link are collected using the PubMed related articles algorithm to identify records with similar terminology to the OMIM record.
OMIM (cited)
Online Mendelian Inheritance in Man (OMIM) records that include the current articles as reference cited at the end of the OMIM record.
Protein (Weighted)
Protein records associated with the current articles through related Gene database records. These are the related sequences on the Gene record that are added manually by NCBI.
Cited in PMC
Full-text articles in the PubMed Central Database that cite the current articles.
Cited in Books
NCBI Bookshelf books that cite the current articles.

Recent activity

Clear Turn Off Turn On

Mucopolysaccharide storage disease in three families of cats with arylsulfatase ...
Mucopolysaccharide storage disease in three families of cats with arylsulfatase B deficiency: leukocyte studies and carrier identification.
Pediatr Res. 1979 Nov ;13(11):1203-10.

PubMed
Isolation of Borrelia burgdorferi from the myocardium of a patient with longstan...
Isolation of Borrelia burgdorferi from the myocardium of a patient with longstanding cardiomyopathy.
N Engl J Med. 1990 Jan 25 ;322(4):249-52.

PubMed
A pilot study of medical student 'abuse'. Student perceptions of mistreatment an...
A pilot study of medical student 'abuse'. Student perceptions of mistreatment and misconduct in medical school.
JAMA. 1990 Jan 26 ;263(4):533-7.

PubMed
[Quantum analysis of postsynaptic potentials].
[Quantum analysis of postsynaptic potentials].
Neirofiziologiia. 1979 ;11(5):491-505.

PubMed
From the Food and Drug Administration.
From the Food and Drug Administration.
JAMA. 1990 Jan 12 ;263(2):202.

PubMed

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PubMed

Result Filters

Display Settings:

Send to:

Mucopolysaccharide storage disease in three families of cats with arylsulfatase B deficiency: leukocyte studies and carrier identification.

Publication Types, MeSH Terms, Substances

Publication Types

MeSH Terms

Substances

LinkOut - more resources

Full Text Sources

Other Literature Sources

Supplemental Content

Save items

Related citations in PubMed

Cited by 11 PubMed Central articles

Related information

Recent activity

Simple NCBI Directory

Getting Started

Resources

Popular

Featured

NCBI Information