A familial occurrence of a mucopolysaccharidosis: Hurler's or Hunter's syndrome?
作者信息
Bhambhani R, Singh S M, Kuspira J, Muntjewerff N
出版信息
Hum Hered. 1974;24(2):219-24. doi: 10.1159/000152654.
PMID:4213627
Abstract
摘要
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1
A familial occurrence of a mucopolysaccharidosis: Hurler's or Hunter's syndrome?黏多糖贮积症的家族性发病：胡尔勒综合征还是亨特综合征？
Hum Hered. 1974;24(2):219-24. doi: 10.1159/000152654.
2
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3
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4
Hurler's, Hunter's and Morquio's syndromes. A biochemical study in the light of current views of the underlying defects.胡勒氏综合征、亨特氏综合征和莫尔基奥氏综合征。基于对潜在缺陷的当前观点的生化研究。
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5
The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome).Xm血清系统基因座与X连锁型胡尔勒综合征（亨特综合征）的连锁关系。
Am J Hum Genet. 1968 Jul;20(4):398-401.
6
Intrauterine diagnosis of the hurler and hunter syndromes.黏多糖贮积症Ⅰ型和Ⅱ型的宫内诊断。
N Engl J Med. 1969 Mar 27;280(13):686-8. doi: 10.1056/NEJM196903272801303.
7
Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.亨特综合征携带者的诊断；在有或没有1-磷酸果糖存在的情况下，放射性硫酸盐掺入成纤维细胞。
Hum Genet. 1982;60(2):167-71. doi: 10.1007/BF00569706.
8
[Unusual findings in 2 patients with Hunter's disease].[2例亨廷顿病患者的异常发现]
Dtsch Gesundheitsw. 1970 Jan 16;25(2):78-82.
9
[Familial cases of Hunter's syndrome].[亨特综合征的家族性病例]
Nihon Rinsho. 1973 Aug 10;31(8):2606-9.
10
[Hunter's disease: study of a family from the plain of Paestum].
Acta Neurol (Napoli). 1973 May-Jun;28(3):323-49.
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