Works matching IS 08830738 AND DT 1992 AND VI 7 AND IP 1S
Results: 17
Treatment of Inherited Neurometabolic Diseases: The Future.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S132, doi. 10.1177/088307389200700117
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- Article
CT and MRI of the Brain in Inherited Neurometabolic Disorders.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S112, doi. 10.1177/088307389200700116
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- Article
Dietary Management of Inborn Errors of Amino Acid Metabolism With Protein-Modified Diets.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S92, doi. 10.1177/088307389200700115
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- Article
A Patient With Propionic Acidemia Managed With Continuous Insulin Infusion and Total Parenteral Nutrition.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S88, doi. 10.1177/088307389200700114
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- Article
Increased Radiosensitivity of Cell Lines Derived From a Down's Syndrome Patient With Ocular Telangiectasia.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S83, doi. 10.1177/088307389200700113
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- Article
Riyadh Chromosome Breakage Syndrome: Mental Retardation With Depigmentation of the Skin and Hair.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S79, doi. 10.1177/088307389200700112
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- Article
Coincident Neuraminidase and Aspartoacylase Deficiency Associated With Chromosome 9Q Paracentric Inversion in a Saudi Family.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S73, doi. 10.1177/088307389200700111
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- Article
Coping With an Affected Birth: Genetic Counseling in Saudi Arabia.
- Published in:
- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S69, doi. 10.1177/088307389200700110
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- Article
Unknown Dysmorphic Syndromes and Developmental Delay in Saudi Arabia.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S64, doi. 10.1177/088307389200700109
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- Article
Congenital Muscular Dystrophy With Abnormal Radiographic Myelin Pattern.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S51, doi. 10.1177/088307389200700108
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- Article
G M1 Gangliosidosis Type 2 in Two Siblings.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S41, doi. 10.1177/088307389200700107
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- Article
Heterogeneity of Carboxypeptidase Activity in Infantile-Onset Galactosialidosis.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S31, doi. 10.1177/088307389200700106
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- Article
Response of 6-Pyruvoyltetrahydropterin Synthase Deficiency to Tetrahydrobiopterin.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S26, doi. 10.1177/088307389200700105
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- Publication type:
- Article
Biochemical Heterogeneity of Infantile Central Nervous System Spongy Degeneration.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S22, doi. 10.1177/088307389200700104
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- Article
Saudi Variant of Multiple Sulfatase Deficiency.
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- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S12, doi. 10.1177/088307389200700103
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- Article
Preface.
- Published in:
- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S2, doi. 10.1177/088307389200700101
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- Article
Neurometabolic Diseases at a National Referral Center: Five Years Experience at the King Faisal Specialist Hospital and Research Centre.
- Published in:
- Journal of Child Neurology, 1992, v. 7, n. 1S, p. S4, doi. 10.1177/088307389200700102
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- Article