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Biochemical Basis of Late-Onset Neurolipidoses.
- Published in:
- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 197, doi. 10.1159/000112160
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- Article
Introduction.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 185, doi. 10.1159/000112157
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- Article
The First Alzheimer Disease Case: A Metachromatic Leukodystrophy?
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 186, doi. 10.1159/000112158
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- Article
Diagnosis and Pathogenesis of Late-Onset Genetic Metabolic Encephaloneuromyopathies.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 188, doi. 10.1159/000112159
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- Article
Title Page / Table of Contents.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 181, doi. 10.1159/000112156
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- Article
Neuropathology of Late Onset Gangliosidoses.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 205, doi. 10.1159/000112161
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- Article
Adult Forms of Metachromatic Leukodystrophy: Clinical and Biochemical Approach.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 211, doi. 10.1159/000112162
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- Article
Pseudodeficiencies of Arylsulfatase A and Galactocerebrosidase Activities.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 216, doi. 10.1159/000112163
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- Article
Molecular Genetics of Metachromatic Leukodystrophy.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 222, doi. 10.1159/000112164
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- Article
Phenotypic Consequences of Low Arylsulfatase A Genotypes (ASAp/ASAp and ASA<sup>-</sup>/ASAp): Does There Exist an Association with Multiple Sclerosis?
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 228, doi. 10.1159/000112165
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- Article
Late-Onset Krabbe Disease (Globoid Cell Leukodystrophy): Clinical and Biochemical Features of 15 Cases.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 232, doi. 10.1159/000112166
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- Article
Symptomatology of Late Onset Krabbe's Leukodystrophy: The European Experience.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 240, doi. 10.1159/000112167
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- Article
Sialic Acid Storage Disorders: Observations on Clinical and Biochemical Variation.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 327, doi. 10.1159/000112181
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- Article
Clinical Aspects of Adrenoleukodystrophy and Adrenomyeloneuropathy.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 254, doi. 10.1159/000112170
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- Article
Cognitive Function in Adult Adrenoleukodystrophy: Comparison with Leukoaraiosis and Multiple Sclerosis.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 251, doi. 10.1159/000112169
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- Publication type:
- Article
Recent Biochemical and Genetic Advances in Our Understanding of Batten's Disease (Ceroid-Lipofuscinosis).
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 339, doi. 10.1159/000112183
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- Article
Cherry-Red Spot Myoclonus Syndrome (Type I Sialidosis).
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 320, doi. 10.1159/000112180
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- Article
Leuko-Araiosis.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 245, doi. 10.1159/000112168
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- Article
Adult Type of Neuronal Ceroid Lipofuscinosis.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 331, doi. 10.1159/000112182
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- Article
Peroxisomal Fatty Acid β-Oxidation in Relation to Adrenoleukodystrophy.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 262, doi. 10.1159/000112171
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- Article
The Clinical Aspects of Adult Hexosaminidase Deficiencies.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 280, doi. 10.1159/000112174
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- Article
Schilder's Diffuse Sclerosis.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 267, doi. 10.1159/000112172
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- Article
Experience on Therapy of Adrenoleukodystrophy and Adrenomyeloneuropathy.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 274, doi. 10.1159/000112173
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- Publication type:
- Article
Biochemical and Molecular Aspects of Late-Onset GM2-Gangliosidosis: B1 Variant as a Prototype.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 288, doi. 10.1159/000112175
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- Article
Molecular and Clinical Heterogeneity of Adult G<sub>M</sub><sub>2</sub> Gangliosidosis.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 295, doi. 10.1159/000112200
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- Article
Clinical and Molecular Heterogeneity in Hereditary β-Galactosidase Deficiency.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 299, doi. 10.1159/000112201
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- Article
Clinical Aspects of Niemann-Pick Type C Disease in the Adult.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 304, doi. 10.1159/000112177
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- Article
Type C Niemann-Pick Disease: Biochemical Aspects and Phenotypic Heterogeneity.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 307, doi. 10.1159/000112178
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- Article
Type C Niemann-Pick Disease: Use of Hydrophobic Amines to Study Defective Cholesterol Transport.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 315, doi. 10.1159/000112179
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- Article
Molecular Aspects of Gaucher Disease.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 352, doi. 10.1159/000112185
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- Article
Norrbottnian Type of Gaucher Disease - Clinical, Biochemical and Molecular Biology Aspects: Successful Treatment with Bone Marrow Transplantation.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 345, doi. 10.1159/000112184
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- Article
Biochemical Abnormalities in Cerebrotendinous Xanthomatosis.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 363, doi. 10.1159/000112186
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- Article
Cerebrotendinous Xanthomatous as a Multisystem Disease Mimicking Premature Ageing.
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- Developmental Neuroscience, 1991, v. 13, n. 4/5, p. 371, doi. 10.1159/000112187
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- Article