(Q33903446)

29 July 2017

title

Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy (English)

1 reference

metachromatic leukodystrophy

29 July 2017

main subject

1 reference

inferred from title

author

Ingeborg Krägeloh-Mann

9

object named as

Ingeborg Krägeloh-Mann

1 reference

29 July 2017

Christian Krarup

6

1 reference

ORCID Public Data File 2021

author name string

Samuel Groeschel

1

1 reference

29 July 2017

Christine í Dali

2

1 reference

29 July 2017

Philipp Clas

3

1 reference

29 July 2017

Judith Böhringer

4

1 reference

29 July 2017

Morten Duno

5

1 reference

29 July 2017

Christiane Kehrer

7

1 reference

29 July 2017

Marko Wilke

8

1 reference

29 July 2017

language of work or name

English

0 references

publication date

19 September 2012

1 reference

29 July 2017

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29 July 2017

volume

79

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29 July 2017

issue

16

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29 July 2017

page(s)

1662-1670

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INFANTILE METACHROMATIC LEUCODYSTROPHY.

29 July 2017

cites work

1 reference

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Brain N-acetylaspartate levels correlate with motor function in metachromatic leukodystrophy.

5 July 2018

1 reference

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Metachromatic leukodystrophy--an update

5 July 2018

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Axon-oligodendrocyte interactions during developmental myelination, demyelination and repair

5 July 2018

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Leukodystrophies with late disease onset: an update

5 July 2018

1 reference

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Metachromatic leukodystrophy: a scoring system for brain MR imaging observations

5 July 2018

1 reference

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Intraclass correlations: uses in assessing rater reliability

5 July 2018

1 reference

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Metachromatic leukodystrophy: genetics, pathogenesis and therapeutic options

5 July 2018

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5 July 2018

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User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability

5 July 2018

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5 July 2018

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Computer-assisted imaging to assess brain structure in healthy and diseased brains

5 July 2018

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A voxel-based morphometric study of ageing in 465 normal adult human brains

5 July 2018

1 reference

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Characterization of four arylsulfatase A missense mutations G86D, Y201C, D255H, and E312D causing metachromatic leukodystrophy

5 July 2018

1 reference

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Molecular basis of late infantile metachromatic leukodystrophy in the Habbanite Jews

5 July 2018

1 reference

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Ultrastructural study of neurons in metachromatic leukodystrophy

5 July 2018

1 reference

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Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy

5 July 2018

1 reference

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Molecular basis of different forms of metachromatic leukodystrophy

5 July 2018

1 reference

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A semi-automatic algorithm for determining the demyelination load in metachromatic leukodystrophy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

The natural course of gross motor deterioration in metachromatic leukodystrophy

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Developmental changes in cerebral grey and white matter volume from infancy to adulthood.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Characterization of new arylsulfatase A gene mutations reinforces genotype-phenotype correlation in metachromatic leukodystrophy.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

An evaluation of four automatic methods of segmenting the subcortical structures in the brain.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Molecular and clinical consequences of novel mutations in the arylsulfatase A gene.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Template-O-Matic: a toolbox for creating customized pediatric templates

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

The NIH MRI study of normal brain development

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Histopathologic correlates of radial stripes on MR images in lysosomal storage disorders.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Late infantile metachromatic leuco-encephalopathy, with primary degeneration of the interfascicular oligodendroglia.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Infantile metachromatic leukodystrophy. (Greenfield's disease).

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Metachromatic leukodystrophy: a 12-bp deletion in exon 2 of the arylsulfatase A gene in a late infantile variant

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

The role of oligodendrocytes and myelin on axon maturation in the developing rat retinofugal pathway.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4098858

Formation of compact myelin is required for maturation of the axonal cytoskeleton

29 October 2018

1 reference

12 December 2020

A 9-bp deletion (2320del9) on the background of the arylsulfatase A pseudodeficiency allele in a metachromatic leukodystrophy patient and in a patient with nonprogressive neurological symptoms

1 reference

12 December 2020

Identification of nine novel arylsulfatase a (ARSA) gene mutations in patients with metachromatic leukodystrophy (MLD)

1 reference

12 December 2020

Metachromatic leukodystrophy: identification of the first deletion in exon 1 and of nine novel point mutations in the arylsulfatase A gene

1 reference

12 December 2020

Metachromatic leukodystrophy: subtype genotype/phenotype correlations and identification of novel missense mutations (P148L and P191T) causing the juvenile-onset disease

1 reference

12 December 2020

10.1212/WNL.0B013E31826E9AD2

Identifiers

DOI

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29 July 2017

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29 July 2017

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