发表于 2025-3-23 10:03:50

http://reply.papertrans.cn/88/8798/879749/879749_11.png

Anal-Canal 发表于 2025-3-23 15:10:49

http://reply.papertrans.cn/88/8798/879749/879749_12.png

调整 发表于 2025-3-23 18:23:59

Monogenic Disorder: Fabry Disease, white matter lesions, pulvinar hyperintensity on T1-weighted images and vascular dolichoectasia. Enzyme replacement therapy has revolutionized the management of fabry disease, but its role in stroke prevention remains unclear.

延期 发表于 2025-3-24 01:02:46

http://reply.papertrans.cn/88/8798/879749/879749_14.png

mitral-valve 发表于 2025-3-24 05:54:43

http://reply.papertrans.cn/88/8798/879749/879749_15.png

不愿 发表于 2025-3-24 08:42:50

http://reply.papertrans.cn/88/8798/879749/879749_16.png

Ornament 发表于 2025-3-24 11:11:45

http://reply.papertrans.cn/88/8798/879749/879749_17.png

leniency 发表于 2025-3-24 15:13:14

http://reply.papertrans.cn/88/8798/879749/879749_18.png

TEN 发表于 2025-3-24 19:28:30

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASILthe different types of cerebral small vessel disease . Up to 1993, several families with hereditary cerebral small artery disease mimicking manifestations observed in CADASIL were reported using numerous eponyms; “Chronic familial vascular encephalopathy” , “Familiäre zerebrale arterioskler

Nerve-Block 发表于 2025-3-25 00:49:51

Monogenic Disorder: Fabry Disease,, along with non-neurological features. Later, life-threatening complications include renal failure, heart disease, and young-onset stroke. However, patients can present with stroke before a diagnosis of fabry disease has been reached. Despite its mode of inheritance, women with fabry disease may be
页: 1 [2] 3 4 5 6
查看完整版本: Titlebook: Stroke Genetics; Pankaj Sharma,James F. Meschia Book 20172nd edition The Editor(s) (if applicable) and The Author(s), under exclusive lice