(Q41667386)

6 October 2017

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title

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

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6 October 2017

Baslow MH

1

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6 October 2017

Resnik TR

series ordinal

2

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6 October 2017

publication date

1 October 1997

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Journal of Molecular Neuroscience

6 October 2017

published in

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6 October 2017

volume

9

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6 October 2017

issue

2

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6 October 2017

page(s)

109-125

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https://scigraph.springernature.com/pub.10.1007/bf02736855

6 October 2017

exact match

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cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FBF02736855

SCHILDER'S ENCEPHALITIS PERIAXIALIS DIFFUSA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02736855

Neuroexcitatory plasma amino acids are elevated in migraine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02736855

Partial purification and characterization of histidine acetyltransferase in brain of Nile tilapia (Oreochromis niloticus).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF02736855

A review of phylogenetic and metabolic relationships between the acylamino acids, N-acetyl-L-aspartic acid and N-acetyl-L-histidine, in the vertebrate nervous system.

21 January 2018

1 reference

12 December 2020

Identification and expression of eight novel mutations among non-Jewish patients with Canavan disease

1 reference

12 December 2020

N-acetyl-L-aspartic acid: a literature review of a compound prominent in 1H-NMR spectroscopic studies of brain

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal detection of Canavan disease (aspartoacylase deficiency) by DNA analysis

1 reference

12 December 2020

The molecular basis of canavan (aspartoacylase deficiency) disease in European non-Jewish patients

1 reference

12 December 2020

Measurement of human brain aspartate N-acetyl transferase flux in vivo

1 reference

12 December 2020

Canavan gene therapy protocol

1 reference

12 December 2020

Huntington's disease: the neuroexcitotoxin aspartate is increased in platelets and decreased in plasma.

1 reference

12 December 2020

Identification of N-acetylaspartate in the lens of the vertebrate eye: a new model for the investigation of the function of N-acetylated amino acids in vertebrates

1 reference

12 December 2020

The participation of N-acetyl-L-aspartic acid in brain metabolism.

1 reference

12 December 2020

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

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12 December 2020

N-Acetylation of L-aspartate in the nervous system: differential distribution of a specific enzyme.

1 reference

12 December 2020

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

1 reference

12 December 2020

Excitatory amino acids in cerebrospinal fluid in neonatal asphyxia.

1 reference

12 December 2020

Distribution of free amino acids and related compounds in ocular fluids, lens, and plasma of various mammalian species.

1 reference

12 December 2020

Studies on the free amino acids and related compounds in the tissues of the cat

1 reference

12 December 2020

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

1 reference

12 December 2020

Purification, characterization, and localization of aspartoacylase from bovine brain

1 reference

12 December 2020

Study of antioxidant properties of metal aspartates

1 reference

12 December 2020

Canavan disease: biochemical and molecular studies

1 reference

12 December 2020

SSIEM Award. Aspartoacylase deficiency: the enzyme defect in Canavan disease

1 reference

12 December 2020

Prenatal detection of Canavan disease by measurement of N-acetyl-L-aspartate in amniotic fluid.

1 reference

12 December 2020

Specific expression of N-acetylaspartate in neurons, oligodendrocyte-type-2 astrocyte progenitors, and immature oligodendrocytes in vitro.

1 reference

12 December 2020

Gene therapy in New Zealand

1 reference

12 December 2020

Determination of N-acetylaspartic acid in human cerebrospinal fluid by gas chromatography-mass spectrometry

1 reference

12 December 2020

Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolution.

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

Metabolism of N-acetyl-L-aspartic acid in mice.

1 reference

12 December 2020

Brain uptake of radiolabeled amino acids, amines, and hexoses after arterial injection

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12 December 2020

The occurrence of N-acetylaspartate amidohydrolase (Aminoacylase II) in the developing rat

1 reference

12 December 2020

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

1 reference

12 December 2020

Canavan disease: from spongy degeneration to molecular analysis

1 reference

12 December 2020

Role of amino acid transport and countertransport in nutrition and metabolism

1 reference

12 December 2020

Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): comparison of enzymatic and metabolite analysis

1 reference

12 December 2020

Canavan disease: mutations among Jewish and non-Jewish patients

1 reference

12 December 2020

Extracellular overflow of neuroactive amino acids during severe insulin-induced hypoglycemia: in vivo dialysis of the rat hippocampus.

1 reference

12 December 2020

Protracted form of Canavan's disease: case history and protein kinase activity of membrane fractions.

1 reference

12 December 2020

Brain amino acid reductions in one family with chromosome 6p?linked dominantly inherited olivopontocerebellar atrophy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02736855

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Dimensions Publication ID

6 October 2017

1009838304

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1 reference