Type Ⅰ sialidosis: a case report
Yinchao LI; Shuda CHEN; Xianyue LIU; Yiran ZHAO; Chengzhe WANG; Liemin ZHOU.
Chinese Journal of Neurology
; (12): 251-254, 2021.
Artículo en Zh | WPRIM | ID: wpr-885410
Documentos relacionados
Bergmeister's papilla in a young patient with type 1 sialidosis: case report.
Cardiovascular involvement in alpha-n-acetyl neuraminidase deficiency syndromes (sialidosis type I and II).
Type 1 Sialidosis Patient With a Novel Deletion Mutation in the NEU1 Gene: Case Report and Literature Review.
Type I sialidosis, a normosomatic lysosomal disease, in the differential diagnosis of late-onset ataxia and myoclonus: An overview.
Unraveling mucolipidosis type III gamma through whole genome sequencing in late-onset retinitis pigmentosa: a case report.
First report of two Taiwanese siblings with sialidosis type I: a 10-year follow-up study.
Sialidosis type I: ophthalmological findings.
Clinical and electrophysiological characteristics of a type 1 sialidosis patient with a novel deletion mutation in NEU1 gene.
Fundus autofluorescence and optical coherence tomography of a macular cherry-red spot in a case report of sialidosis.
Mucolipidosis type II and type III: a systematic review of 843 published cases.