Atypical clinical and radiological course of a patient with Canavan disease. (Q52146663)

23 April 2018

title

Atypical clinical and radiological course of a patient with Canavan disease. (English)

1 reference

23 April 2018

author name string

Catherine Sarret

series ordinal

1

1 reference

23 April 2018

Odile Boespflug-Tanguy

series ordinal

2

1 reference

23 April 2018

Diana Rodriguez

series ordinal

3

1 reference

23 April 2018

publication date

19 November 2015

1 reference

23 April 2018

published in

Metabolic Brain Disease

1 reference

23 April 2018

volume

31

1 reference

23 April 2018

page(s)

475-479

1 reference

23 April 2018

issue

2

1 reference

23 April 2018

https://scigraph.springernature.com/pub.10.1007/s11011-015-9767-9

exact match

0 references

cites work

Canavan disease, a rare early-onset human spongiform leukodystrophy: insights into its genesis and possible clinical interventions

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Dietary triheptanoin rescues oligodendrocyte loss, dysmyelination and motor function in the nur7 mouse model of Canavan disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Ablating N-acetylaspartate prevents leukodystrophy in a Canavan disease model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Mutational analysis of aspartoacylase: implications for Canavan disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Canavan disease: clinical features and recent advances in research.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Mild-onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Axon-glial signaling and the glial support of axon function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Canavan disease - unusual imaging features in a child with mild clinical presentation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Homozygosity for mutation G212A of the gene for aspartoacylase is associated with atypical form of Canavan's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Quantitative measurements with localized 1H MR spectroscopy in children with Canavan's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Atypical MRI findings in Canavan disease: a patient with a mild course

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

Moro reflex profile in high-risk infants at the first year of life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11011-015-9767-9

The spectrum of mutations of the aspartoacylase gene in Canavan disease in non-Jewish patients

21 January 2018

1 reference

12 December 2020

Magnetic resonance imaging in juvenile Canavan disease

1 reference

12 December 2020

Protracted course of N-acetylaspartic aciduria in two non-Jewish siblings: identical clinical and magnetic resonance imaging findings.

1 reference

12 December 2020

Case 99: Canavan disease

1 reference

12 December 2020

10.1007/S11011-015-9767-9

Identifiers

DOI

1 reference

23 April 2018

PubMed ID

26586007

1 reference

23 April 2018