James H. Austin, MD, Harvard University - Publications
Affiliations: | Neurology | University of Missouri-Columbia, Columbia, MO |
Area:
neurochemistry, neuropharmacology, and clinical neurology.Website:
http://en.wikipedia.org/wiki/James_H._AustinYear | Citation | Score | |||
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1973 | Stumpf DA, Austin JH, Crocker AC, LaFrance M. Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues. American Journal of Diseases of Children (1960). 126: 747-55. PMID 4271367 DOI: 10.1001/Archpedi.1973.02110190597003 | 0.565 | |||
1973 | Austin JH. Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency. Archives of Neurology. 28: 258-64. PMID 4265903 DOI: 10.1001/Archneur.1973.00490220066010 | 0.365 | |||
1971 | Stumpf D, Austin J. Metachromatic Leukodystrophy (MLD): IX. Qualitative and Quantitative Differences in Urinary Arylsulfatase A in Different Forms of MLD Jama Neurology. 24: 117-124. PMID 5540376 DOI: 10.1001/Archneur.1971.00480320045004 | 0.576 | |||
1970 | Austin J, Suzuki K, Armstrong D, Brady R, Bachhawat BK, Schlenker J, Stumpf D. Studies in Globoid (Krabbe) Leukodystrophy (GLD): V. Controlled Enzymic Studies in Ten Human Cases Jama Neurology. 23: 502-512. PMID 5478272 DOI: 10.1001/Archneur.1970.00480300024003 | 0.583 | |||
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