Quantitative t2 measurements in juvenile and late infantile neuronal ceroid lipofuscinosis.

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CLN3 deficient cells display defects in the ARF1-Cdc42 pathway and actin-dependent events Volumetric Description of Brain Atrophy in Neuronal Ceroid Lipofuscinosis 2: Supratentorial Gray Matter Shows Uniform Disease Progression.

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Quantitative t2 measurements in juvenile and late infantile neuronal ceroid lipofuscinosis.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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name

Quantitative t2 measurements i ...... euronal ceroid lipofuscinosis.

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Quantitative t2 measurements i ...... euronal ceroid lipofuscinosis.

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Quantitative t2 measurements i ...... euronal ceroid lipofuscinosis.

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A Schulz

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Alvaro Paniagua Bravo

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E Goebell

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J Fiehler

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J Sedlacik

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M Rosenkranz

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N D Forkert

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U Löbel

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X Ding

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P2860

Clinical and neuroradiological diagnostic aspects of neuronal ceroid lipofuscinoses disorders.

Decreased T2 signal in the thalami may be a sign of lysosomal storage disease.

Whole brain quantitative T2 MRI across multiple scanners with dual echo FSE: applications to AD, MCI, and normal aging

Correlations between genotype, ultrastructural morphology and clinical phenotype in the neuronal ceroid lipofuscinoses.

The neuronal ceroid-lipofuscinoses.

Current state of clinical and morphological features in human NCL.

A clinical rating scale for Batten disease: reliable and relevant for clinical trials.

MRI of brain iron.

MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type.

Macromolecule content influences proton diffusibility in gliomas.

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P921

Infantile neuronal ceroid lipofuscinosis

Quantitative t2 measurements in juvenile and late infantile neuronal ceroid lipofuscinosis.

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P2860

P2860

Quantitative t2 measurements in juvenile and late infantile neuronal ceroid lipofuscinosis.

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