Lv1
30 积分 2023-12-23 加入
Iowa APP mutation-related hereditary cerebral amyloid angiopathy (CAA): A new family from Spain
1天前
已完结
An APP mutation family exhibiting white matter hyperintensities and cortical calcification in East China
1天前
已完结
A Western Australian kindred with Dutch cerebral amyloid angiopathy
18天前
已完结
Hereditary Cerebral Hemorrhage with Amyloidosis‐Dutch type (HCHWA‐D): II ‐ A Review of Histopathological Aspects
19天前
已完结
Hereditary Cerebral Hemorrhage with Amyloidosis‐Dutch Type (HCHWA‐D): I ‐ A Review of Clinical, Radiologic and Genetic Aspects
19天前
已完结
Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation
21天前
已完结
Histopathologic Analysis of Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): A Report of a New Genetically Confirmed Case and Comparison to 2 Previous Cases
21天前
已完结
Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation
30天前
已完结
Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes
1个月前
已完结
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