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THE NEUROPATHOLOGY OF HEREDITARY DYSTOPIC LIPIDOSIS.

作者信息

RAHMAN A N, LINDENBERG R

出版信息

Arch Neurol. 1963 Oct;9:373-85. doi: 10.1001/archneur.1963.00460100061007.

DOI:10.1001/archneur.1963.00460100061007
PMID:14060085
Abstract
摘要

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引用本文的文献

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Fabry disease: a rare disorder calling for personalized medicine.法布瑞氏病:一种罕见的需要个体化医疗的疾病。
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Neuropsychiatric Symptoms and Their Association With Sex, Age, and Enzyme Replacement Therapy in Fabry Disease: A Systematic Review.法布里病的神经精神症状及其与性别、年龄和酶替代疗法的关联:一项系统综述
Front Psychiatry. 2022 Mar 16;13:829128. doi: 10.3389/fpsyt.2022.829128. eCollection 2022.
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Pathogenesis and Molecular Mechanisms of Anderson-Fabry Disease and Possible New Molecular Addressed Therapeutic Strategies.
安德森-法布里病的发病机制和分子机制及可能的新分子靶向治疗策略。
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Altered pupillary light responses are associated with the severity of autonomic symptoms in patients with Fabry disease.瞳孔光反射改变与法布里病患者自主症状严重程度相关。
Sci Rep. 2021 Apr 14;11(1):8146. doi: 10.1038/s41598-021-87589-x.
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Fabry Disease With Concomitant Lewy Body Disease.伴有路易体病的法布里病。
J Neuropathol Exp Neurol. 2020 Apr 1;79(4):378-392. doi: 10.1093/jnen/nlz139.
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Autonomic neuropathy in Fabry disease: a prospective study using the Autonomic Symptom Profile and cardiovascular autonomic function tests.法布瑞病的自主神经病变:前瞻性研究采用自主症状谱和心血管自主功能测试。
BMC Neurol. 2010 Jun 7;10:38. doi: 10.1186/1471-2377-10-38.
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The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus.弥漫性躯体血管角质瘤(法布里病)的遗传学及其与Xg基因座的连锁关系。
Am J Hum Genet. 1965 Jul;17(4):325-42.
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T1 hyperintensity in the pulvinar: key imaging feature for diagnosis of Fabry disease.丘脑枕T1高信号:法布里病诊断的关键影像特征。
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Mouse models of human lysosomal diseases.人类溶酶体疾病的小鼠模型。
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Basilar artery aneurysm and Anderson-Fabry disease.基底动脉动脉瘤与安德森-法布里病
J Neurol Neurosurg Psychiatry. 1980 Jan;43(1):85-7. doi: 10.1136/jnnp.43.1.85.