Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease. - Wikidata - awgldk - TriplyDB

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

http://www.wikidata.org/entity/Q40215622

about

Clinical picture of EPM1-Unverricht-Lundborg disease Classification and lateralization of temporal lobe epilepsies with and without hippocampal atrophy based on whole-brain automatic MRI segmentation.3D texture analysis reveals imperceptible MRI textural alterations in the thalamus and putamen in progressive myoclonic epilepsy type 1, EPM1.Progressive volume loss and white matter degeneration in cstb-deficient mice: a diffusion tensor and longitudinal volumetry MRI study.Impaired osteoclast homeostasis in the cystatin B-deficient mouse model of progressive myoclonus epilepsy.Human stefin B normal and patho-physiological role: molecular and cellular aspects of amyloid-type aggregation of certain EPM1 mutants.Proline Residues as Switches in Conformational Changes Leading to Amyloid Fibril Formation Alterations of motor cortical excitability and anatomy in Unverricht-Lundborg disease.Cerebellar Involvement in Patients with Mild to Moderate Myoclonus Due to EPM1: Structural and Functional MRI Findings in Comparison with Healthy Controls and Ataxic Patients.Fronto-striatal dysfunction in type 3 familial cortical myoclonic tremor epilepsy occurring during aging.

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P2860

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

http://www.wikidata.org/entity/Q40215622

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

2007年论文

@zh

2007年论文

@zh-cn

name

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

@en

type

label

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

@en

prefLabel

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

@en

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P356

J.1528-1167.2007.01118.X

P1433

P1476

Substantial thalamostriatal dopaminergic defect in Unverricht-Lundborg disease.

@en

P2093

Kjell Någren

http://www.w3.org/2001/XMLSchema#string

Miikka Korja

http://www.w3.org/2001/XMLSchema#string

Reijo J Marttila

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Riitta Parkkola

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Salla Lamusuo

http://www.w3.org/2001/XMLSchema#string

Valtteri Kaasinen

http://www.w3.org/2001/XMLSchema#string

P2860

Statistical parametric maps in functional imaging: A general linear approach

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

Levodopa-induced myoclonus

New insights into the molecular basis of progressive myoclonus epilepsy: a multiprotein complex with cystatin B.

Visualization of the hexagonal lattice in the erythrocyte membrane skeleton.

Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22

Visualization of the protein associations in the erythrocyte membrane skeleton

PET evidence for a role of the basal ganglia in patients with ring chromosome 20 epilepsy.

Distinct nuclear and cytoplasmic localization of caspase cleavage products in two models of induced apoptotic death in dopamine neurons of the substantia nigra.

Common dopaminergic mechanism for epileptic photosensitivity in progressive myoclonus epilepsies.

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1768-1773

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scholarly article

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10.1111/J.1528-1167.2007.01118.X

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9

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48

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6346160

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17484752

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