Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene.
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Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review.Expansion of genetic testing in the division of functional genomics, research center for bioscience and technology, tottori university from 2000 to 2013.Pathogenesis, Emerging therapeutic targets and Treatment in Sialidosis.Sialidosis type I: ophthalmological findings.Cortical damage in the posterior visual pathway in patients with sialidosis type 1.
P2860
Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene.
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2013 nî lūn-bûn
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Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@en
Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@nl
type
label
Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@en
Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@nl
prefLabel
Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@en
Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@nl
P2093
P1433
P1476
Clinical and serial MRI findin ...... nse mutation in the NEU1 gene.
@en
P2093
Aya Narita
Dai Kishida
Eiji Nanba
Kaori Adachi
Kosaku Ohno
Shu-Ichi Ikeda
Yoshiki Sekijima
P304
P356
10.2169/INTERNALMEDICINE.52.8901
P577
2013-01-01T00:00:00Z