Matches in Library of Congress for { ?s ?p Peripheral neuropathies -- The molecular and genetic basis of spinal muscular atrophies -- Congenital myasthenic syndromes -- Dystrophinopathies -- Limb-girdle muscular dystrophies -- The congenital myopathies -- The distal myopathies -- Hereditary inclusion-body myopathies -- The myotonic dystrophies -- Facioscapulohumeral dystrophy -- Ion channel disorders -- The phakomatoses -- Lipoprotein disorders -- Apolipoprotein E: structure and function in lipid metabolism and neurobiology -- Cerebrotendinous xanthomatosis -- Disorders of lipid metabolism -- Glycogen storage diseases -- Disorders of galactose metabolism -- Inborn errors of amino acid metabolism -- Disorders of the urea cycle -- Disorders of glucose transport -- Maple syrup urine disease: clinical biochemical considerations -- Congenital disorders of N-linked glycosylation -- Disorders of glutathione metabolism -- Disorders of purine metabolism -- The porphyrias -- Friedreich ataxia -- Disorders of copper metabolism: Wilson disease and Menkes disease -- Genetic and dietary influences on life span -- Vitamins: cobalamin and folate -- Disorders of biotin metabolism: treatable neurologic syndromes -- Psychiatric diseases: challenges in psychiatric genetics -- Depression -- Bipolar disorder -- Schizophrenia -- Obessive-compulsive disorder and tourette syndrome -- Genetic bases of addictive behaviors -- Autism -- A neurologic gene map.. }
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- 2007020775 description "Peripheral neuropathies -- The molecular and genetic basis of spinal muscular atrophies -- Congenital myasthenic syndromes -- Dystrophinopathies -- Limb-girdle muscular dystrophies -- The congenital myopathies -- The distal myopathies -- Hereditary inclusion-body myopathies -- The myotonic dystrophies -- Facioscapulohumeral dystrophy -- Ion channel disorders -- The phakomatoses -- Lipoprotein disorders -- Apolipoprotein E: structure and function in lipid metabolism and neurobiology -- Cerebrotendinous xanthomatosis -- Disorders of lipid metabolism -- Glycogen storage diseases -- Disorders of galactose metabolism -- Inborn errors of amino acid metabolism -- Disorders of the urea cycle -- Disorders of glucose transport -- Maple syrup urine disease: clinical biochemical considerations -- Congenital disorders of N-linked glycosylation -- Disorders of glutathione metabolism -- Disorders of purine metabolism -- The porphyrias -- Friedreich ataxia -- Disorders of copper metabolism: Wilson disease and Menkes disease -- Genetic and dietary influences on life span -- Vitamins: cobalamin and folate -- Disorders of biotin metabolism: treatable neurologic syndromes -- Psychiatric diseases: challenges in psychiatric genetics -- Depression -- Bipolar disorder -- Schizophrenia -- Obessive-compulsive disorder and tourette syndrome -- Genetic bases of addictive behaviors -- Autism -- A neurologic gene map.".
- 2007020775 tableOfContents "Peripheral neuropathies -- The molecular and genetic basis of spinal muscular atrophies -- Congenital myasthenic syndromes -- Dystrophinopathies -- Limb-girdle muscular dystrophies -- The congenital myopathies -- The distal myopathies -- Hereditary inclusion-body myopathies -- The myotonic dystrophies -- Facioscapulohumeral dystrophy -- Ion channel disorders -- The phakomatoses -- Lipoprotein disorders -- Apolipoprotein E: structure and function in lipid metabolism and neurobiology -- Cerebrotendinous xanthomatosis -- Disorders of lipid metabolism -- Glycogen storage diseases -- Disorders of galactose metabolism -- Inborn errors of amino acid metabolism -- Disorders of the urea cycle -- Disorders of glucose transport -- Maple syrup urine disease: clinical biochemical considerations -- Congenital disorders of N-linked glycosylation -- Disorders of glutathione metabolism -- Disorders of purine metabolism -- The porphyrias -- Friedreich ataxia -- Disorders of copper metabolism: Wilson disease and Menkes disease -- Genetic and dietary influences on life span -- Vitamins: cobalamin and folate -- Disorders of biotin metabolism: treatable neurologic syndromes -- Psychiatric diseases: challenges in psychiatric genetics -- Depression -- Bipolar disorder -- Schizophrenia -- Obessive-compulsive disorder and tourette syndrome -- Genetic bases of addictive behaviors -- Autism -- A neurologic gene map.".