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[Oligophrenia combined with congenital cataracts. Contribution to the metabolic anomaly of Sjögren's syndrome].

作者信息

Engels H J

出版信息

Arch Psychiatr Nervenkr (1970). 1966;208(1):91-106. doi: 10.1007/BF00341698.

DOI:10.1007/BF00341698
PMID:5968200
Abstract
摘要

相似文献

1
[Oligophrenia combined with congenital cataracts. Contribution to the metabolic anomaly of Sjögren's syndrome].[智力发育不全合并先天性白内障。对干燥综合征代谢异常的贡献]
Arch Psychiatr Nervenkr (1970). 1966;208(1):91-106. doi: 10.1007/BF00341698.
2
Acetylator phenotypes in primary Sjögren's syndrome.
Br J Rheumatol. 1994 Apr;33(4):405-6. doi: 10.1093/rheumatology/33.4.405.
3
Proteomic diagnosis of Sjögren's syndrome.干燥综合征的蛋白质组学诊断
Expert Rev Proteomics. 2007 Dec;4(6):757-67. doi: 10.1586/14789450.4.6.757.
4
Y RNA derived small RNAs in Sjögren's syndrome: Candidate biomarkers?干燥综合征中的 Y RNA 衍生的小 RNA:候选生物标志物?
Int J Rheum Dis. 2017 Nov;20(11):1763-1766. doi: 10.1111/1756-185X.13229. Epub 2017 Nov 19.
5
[A case of Sjögren's reticulated macular dystrophy].[一例干燥综合征网状黄斑营养不良病例]
Rev Med Chir Soc Med Nat Iasi. 1987 Oct-Dec;91(4):767-8.
6
DNA hypermethylation leads to lower FOXP3 expression in CD4+ T cells of patients with primary Sjögren's syndrome.DNA高甲基化导致原发性干燥综合征患者CD4+ T细胞中FOXP3表达降低。
Clin Immunol. 2013 Aug;148(2):254-7. doi: 10.1016/j.clim.2013.05.005. Epub 2013 May 22.
7
[Current aspects of Gougerot-Sjõgren syndrome].[ Gougerot-Sjõgren综合征的当前研究进展]
J Fr Ophtalmol. 1999 Oct;22(8):889-92.
8
The first case of monozygotic twin boys with nearly identical features of Sjögren's syndrome.首例具有几乎相同干燥综合征特征的单卵双胞胎男孩。
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9
[The value of salivary beta 2 microglobulin concentration for diagnosis of Sjögren's syndrome].唾液β2微球蛋白浓度在干燥综合征诊断中的价值
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1997 Feb;19(1):72-4.
10
Sjögren's Syndrome: Animal Models, Etiology, Pathogenesis, Clinical Subtypes, and Diagnosis.干燥综合征:动物模型、病因、发病机制、临床亚型及诊断
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本文引用的文献

1
Congenital encephalo-ophthalmic dysplasia.先天性脑眼发育异常
Arch Ophthal. 1946 Oct;36(4):387-44. doi: 10.1001/archopht.1946.00890210395001.
2
[Oligophrenia and cataracts].[智力发育迟缓与白内障]
Arch Fr Pediatr. 1947;4(6):638.
3
[Sjögren's disease].[干燥综合征]
Ann Med Psychol (Paris). 1952 Jan;110(1 1):65-7.
4
Familial cataract and mental deficiency.家族性白内障与智力缺陷。
Lancet. 1952 Apr 5;1(6710):694-6. doi: 10.1016/s0140-6736(52)90453-4.
5
Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity.有机酸尿症、肾脏氨生成减少、眼球积水和智力迟钝;一种临床病症。
AMA Am J Dis Child. 1952 Feb;83(2):164-84. doi: 10.1001/archpedi.1952.02040060030004.
6
Hereditary congenital spinocerebellar ataxia accompanied by congenital cataract and oligophrenia; a genetic and clinical investigation.伴有先天性白内障和智力发育迟缓的遗传性先天性脊髓小脑共济失调;一项遗传学和临床研究。
Confin Neurol. 1950;10(5):293-308.
7
AETIOLOGY OF CATARACTS IN CHILDHOOD.
Lancet. 1965 May 22;1(7395):1084-6. doi: 10.1016/s0140-6736(65)92672-3.
8
[RECENT RESULTS OF MEDICAL GENETICS, ESPECIALLY IN THE NEUROPSYCHIATRIC SECTOR].[医学遗传学的最新成果,尤其是在神经精神领域]
Wien Klin Wochenschr. 1964 Mar 6;76:165-70.
9
Oligophrenia in combination with congenital ichthyosis and spastic disorders; a clinical and genetic study.智力发育迟缓合并先天性鱼鳞病和痉挛性疾病;一项临床与遗传学研究。
Acta Psychiatr Neurol Scand Suppl. 1957;113:1-112.
10
[Cataract and oligophrenia].[白内障与智力发育不全]
Bull Mem Soc Fr Ophtalmol. 1954;67:318-24; discussion, 324-7.