Congenital metachromatic leukodystrophy

Author:

Bubis J. J.,Adlesberg L.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Reference13 articles.

1. Abraham, K., andP. Lampert: Intraneuronal lipid deposits in metachromatic leukodystrophy, Histochemical and topographical observations. Neurology (Minneap.)13, 686–692 (1963).

2. Austin, J. H.: Metachromatic form of diffuse cerebral sclerosis. I. Diagnosis during life by urine sediment examination. Neurology (Minneap.)7, 415–426 (1957).

3. Black, J. W., andJ. N. Cumings: Infantile metachromatic leukodystrophy. J. Neurol. Neurosurg. Psychiat.24, 233–239 (1961).

4. Einarson, L., andA. V. Neel: Contribution to the study of diffuse brain sclerosis with a comprehensive review of the problem in general and a report of two cases. Acta Jutlandica14 (2), 1–131 (1942).

5. ——, andE. Stromgren: On the problem of diffuse brain sclerosis with special reference to the familial forms. Acta Jutlandica16 (1), 1–178 (1944).

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4. New sites of ocular involvement in late-infantile metachromatic leukodystrophy revealed by histopathologic studies;Graefe's Archive for Clinical and Experimental Ophthalmology;1993-03

5. Pseudoarylsulfatase-A Deficiency in the Neurologically Impaired Patient;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;1985-08

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