(Q34098649)

31 July 2017

title

The burden of inherited leukodystrophies in children (English)

1 reference

31 July 2017

J L Bonkowsky

1

1 reference

31 July 2017

C Nelson

2

1 reference

31 July 2017

J L Kingston

3

1 reference

31 July 2017

F M Filloux

4

1 reference

31 July 2017

M B Mundorff

5

1 reference

31 July 2017

R Srivastava

6

1 reference

31 July 2017

language of work or name

English

0 references

publication date

21 July 2010

1 reference

31 July 2017

1 reference

31 July 2017

volume

75

1 reference

31 July 2017

issue

8

1 reference

31 July 2017

page(s)

718-725

1 reference

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Transplant outcomes in leukodystrophies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Invited article: an MRI-based approach to the diagnosis of white matter disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Metachromatic leukodystrophy: an overview of current and prospective treatments

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Hematopoietic stem cell gene therapy in Hurler syndrome, globoid cell leukodystrophy, metachromatic leukodystrophy and X-adrenoleukodystrophy.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Dental agenesis: genetic and clinical perspectives

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Sensitivity and specificity of decreased CSF asialotransferrin for eIF2B-related disorder

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Delayed tooth eruption: pathogenesis, diagnosis, and treatment. A literature review

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Leukoencephalopathy, cerebral calcifications, and cysts: new observations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

The Social Security Administration's Death Master File: the completeness of death reporting at older ages.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Update on genetic disorders affecting white matter

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Magnetic resonance imaging of inflammatory and demyelinating white-matter diseases of childhood

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

The life expectancy of profoundly handicapped people with mental retardation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

The epidemiology of progressive encephalopathies in childhood. I. Live birth prevalence in west Sweden

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

The Hunter's Hope Krabbe family database

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Alexander disease: ventricular garlands and abnormalities of the medulla and spinal cord.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Clinical and economic outcomes of conventional amphotericin B-associated nephrotoxicity

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Leukodystrophy incidence in Germany.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Adverse drug events in hospitalized patients. Excess length of stay, extra costs, and attributable mortality.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2931652

Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20660364

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20660364

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Survival analysis of haematopoietic cell transplantation for childhood cerebral X-linked adrenoleukodystrophy: a comparison study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20660364

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/WNL.0B013E3181EEE46B

1 reference

31 July 2017

1 reference

31 July 2017

1 reference