(Q34163529)

31 July 2017

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title

Canavan's spongiform leukodystrophy: a clinical anatomy of a genetic metabolic CNS disease (English)

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31 July 2017

Baslow MH

1

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31 July 2017

1 October 2000

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Journal of Molecular Neuroscience

31 July 2017

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31 July 2017

15

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31 July 2017

2

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31 July 2017

61-69

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https://scigraph.springernature.com/pub.10.1385/jmn:15:2:61

31 July 2017

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cites work

Molecular water pumps and the aetiology of Canavan disease: a case of the sorcerer's apprentice

1 reference

12 December 2020

Protracted form of spongy degeneration of the central nervous system: (van Bogaert and Bertrand type)

1 reference

12 December 2020

Global CNS gene transfer for a childhood neurogenetic enzyme deficiency: Canavan disease

1 reference

12 December 2020

The clinical course of Canavan disease.

1 reference

12 December 2020

Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease

1 reference

12 December 2020

Liquid chromatographic-mass spectrometric analysis of N-acetylamino acids in human urine

1 reference

12 December 2020

Functions of N-acetyl-L-aspartate and N-acetyl-L-aspartylglutamate in the vertebrate brain: role in glial cell-specific signaling

1 reference

12 December 2020

The existence of molecular water pumps in the nervous system: a review of the evidence

1 reference

12 December 2020

N-acetylaspartic acid (NAA) and N-acetylaspartylglutamic acid (NAAG) in human ventricular, subarachnoid, and lumbar cerebrospinal fluid.

1 reference

12 December 2020

Canavan disease: diagnosis and molecular analysis

1 reference

12 December 2020

The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination

1 reference

12 December 2020

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

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12 December 2020

Transient elevation of interstitial N-acetylaspartate in reversible global brain ischemia

1 reference

12 December 2020

Inhibition of N-acetylaspartate production: implications for 1H MRS studies in vivo

1 reference

12 December 2020

Biochemistry and molecular biology of Canavan disease

1 reference

12 December 2020

Canavan disease. Analysis of the nature of the metabolic lesions responsible for development of the observed clinical symptoms

1 reference

12 December 2020

Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with canavan disease

1 reference

12 December 2020

N-acetylaspartic aciduria in a child with a progressive cerebral atrophy

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12 December 2020

Purification, characterization, and localization of aspartoacylase from bovine brain

1 reference

12 December 2020

The spongy type of diffuse sclerosis.

1 reference

12 December 2020

Cerebral spongy degeneration of infancy. A biochemical and ultrastructural study of affected twins.

1 reference

12 December 2020

Amidohydrolases of brain; enzymatic hydrolysis of N-acetyl-L-aspartate and other N-acyl-L-amino acids

1 reference

12 December 2020

Studies on the distribution of N-acetyl-L-aspartic acid in brain.

1 reference

12 December 2020

Effects of ethanol and of alcohol dehydrogenase inhibitors on the reduction of N-acetylaspartate levels of brain in mice in vivo: a search for substances that may have therapeutic value in the treatment of Canavan disease.

1 reference

12 December 2020

Extracellular N-acetylaspartate in the rat brain: in vivo determination of basal levels and changes evoked by high K+.

1 reference

12 December 2020

N-acetylaspartic aciduria due to aspartoacylase deficiency--a new aetiology of childhood leukodystrophy

1 reference

12 December 2020

The Enzymatic Synthesis of N-Acetyl-l-aspartic Acid by a Water-insoluble Preparation of a Cat Brain Acetone Powder

1 reference

12 December 2020

N-acetylaspartate as an acetyl source in the nervous system

1 reference

12 December 2020

Transport of N-acetylaspartate by the Na(+)-dependent high-affinity dicarboxylate transporter NaDC3 and its relevance to the expression of the transporter in the brain

1 reference

12 December 2020

Astroglia contain a specific transport mechanism for N-acetyl-L-aspartate.

1 reference

12 December 2020

Canavan disease: mutations among Jewish and non-Jewish patients

1 reference

12 December 2020

Expression of aspartoacylase activity in cultured rat macroglial cells is limited to oligodendrocytes

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12 December 2020

Recent advances in Canavan disease

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12 December 2020

N-acetylaspartylglutamate in Canavan disease: an adverse effector?

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12 December 2020

Specificity of amino acid acylases

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12 December 2020

Embryonic stem cell-derived glial precursors: a source of myelinating transplants

1 reference

12 December 2020

Identifiers

DOI

10.1385/JMN:15:2:61

1 reference

PubMed ID

11220786

Dimensions Publication ID

31 July 2017

0 references

1 reference

PubMed ID

11220786