Brain ultrasound in Canavan disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology Nuclear Medicine and imaging,General Medicine,Internal Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40477-014-0108-3.pdf
Reference15 articles.
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2. Kristjánsdóttir R, Uvebrant P, Wiklund LM (2000) Clinical characteristics of children with cerebral white matter abnormalities. Eur J Paediatr Neurol 4:17–26
3. Gordon N (2001) Canavan disease: a review of recent developments. Eur J Paediatr Neurol 5:65–69
4. Di Pietro V, Cavallari U, Amorini AM, Lazzarino G, Longo S, Poggiani C, Cavalli P, Tavazzi B (2013) New T530C mutation in the aspartoacylase gene caused Canavan disease with no correlation between severity and N-acetylaspartate excretion. Clin Biochem 46:1902–1904
5. Baslow MH (2000) Canavan’s spongiform leukodystrophy: a clinical anatomy of a genetic metabolic CNS disease. J Mol Neurosci 15:61–69
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1. Canavan’s spongiform leukodystrophy (Aspartoacylase deficiency) with emphasis on sonographic features in infancy: description of a case report and review of the literature;Journal of Ultrasound;2022-02-20
2. A Survey Study of Diseases Diagnosed Through Imaging Methodology Using Ultrasonography;Lecture Notes in Electrical Engineering;2020-10-15
3. Canavan disease: An Arab scenario;Gene;2015-04
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