Fast Progression of Cerebellar Atrophy in PLA2G6-Associated Infantile Neuronal Axonal Dystrophy.

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Fast Progression of Cerebellar Atrophy in PLA2G6-Associated Infantile Neuronal Axonal Dystrophy.

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

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name

Fast Progression of Cerebellar ...... ile Neuronal Axonal Dystrophy.

@en

Fast Progression of Cerebellar ...... ile Neuronal Axonal Dystrophy.

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Item

label

Fast Progression of Cerebellar ...... ile Neuronal Axonal Dystrophy.

@en

Fast Progression of Cerebellar ...... ile Neuronal Axonal Dystrophy.

@nl

prefLabel

Fast Progression of Cerebellar ...... ile Neuronal Axonal Dystrophy.

@en

Fast Progression of Cerebellar ...... ile Neuronal Axonal Dystrophy.

@nl

P1476

Fast Progression of Cerebellar ...... tile Neuronal Axonal Dystrophy

@en

P2093

Andrea Bianchi

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Beatrice Berti

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Francesco Mari

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Laura Antonucci

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Mario Mascalchi

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Renzo Guerrini

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P2860

Genetic ablation of PLA2G6 in mice leads to cerebellar atrophy characterized by Purkinje cell loss and glial cell activation

Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysis.

PLA2G6-associated neurodegeneration (PLAN): further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease.

Cerebellar malformations alter regional cerebral development.

Consensus paper: radiological biomarkers of cerebellar diseases

MRI Brain Volume Measurements in Infantile Neuronal Ceroid Lipofuscinosis

Volumetric Description of Brain Atrophy in Neuronal Ceroid Lipofuscinosis 2: Supratentorial Gray Matter Shows Uniform Disease Progression.

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.

Progressive atrophy in the optic pathway and visual cortex of early blind Chinese adults: A voxel-based morphometry magnetic resonance imaging study.

Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients.

P2888

s12311-017-0843-z

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742-745

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scholarly article

P356

10.1007/S12311-017-0843-Z

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2017-06-01T00:00:00Z

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28091863

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