Lv31
330 积分 2024-08-20 加入
A new Italian family with HTRA1 mutation associated with autosomal-dominant variant of CARASIL: Are we pointing towards a disease spectrum?
2天前
已完结
HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade
24天前
已完结
Clinical features and pathogenicity assessment in patients with HTRA1-autosomal dominant disease
4个月前
已完结
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): A challenging diagnosis and a rare multiple sclerosis mimic
4个月前
已完结
HTRA1-related cerebral small-vessel disease causes cerebral microbleeds on the brainstem surface
4个月前
已完结
Hereditary cerebral small vessel disease: Assessment of a HTRA1 variant using protein stability predictors and 3D modelling
4个月前
已完结
[Association analysis of seven single nucleotide polymorphisms identified by genome-wide association study with age-related macular degeneration among ethnic Han Chinese population]
4个月前
已完结
Heterozygous HTRA1 nonsense or frameshift mutations are pathogenic
4个月前
已完结
Beyond the Brain: Systematic Review of Extracerebral Phenotypes Associated With Monogenic Cerebral Small Vessel Disease
4个月前
已完结
Microbleeds in Heterozygous HTRA1-Related Cerebral Small Vessel Disease
4个月前
已完结
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