| scholarly article | Q13442814 |
| P2093 | author name string | K Suzuki | |
| G Wenk | |||
| P2860 | cites work | Menkes kinky-hair disease. A report on its pathology | Q48195408 |
| Letter: Menkes' kinky hair disease treated with subcutaneous copper sulphate | Q48497820 | ||
| Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects | Q48737718 | ||
| Kinky hair disease. I. Clinical and pathological features. | Q51228428 | ||
| Degeneration of the cerebellar system in X-chromosome?linked copper malabsorption | Q66920288 | ||
| Abnormal copper-thionein synthesis and impaired copper utilization in mutated brindled mice: model for Menkes' disease | Q70645610 | ||
| The effect of copper supplementation on the brindled mouse: a clinico-pathological study | Q70664958 | ||
| Increased copper metallothionein in Menkes cultured skin fibroblasts | Q70738653 | ||
| An ultrastructural study on the cerebellum of the brindled mouse | Q71384469 | ||
| Trace element studies in three patients and a fetus with Menkes' disease. Effect of copper therapy | Q71543695 | ||
| Copper infusion therapy in trichopoliodystrophy | Q28337078 | ||
| Primary biochemical defect in copper metabolism in mice with a recessive X-linked mutation analogous to Menkes' disease in man | Q28511239 | ||
| Primary defect in copper transport underlies mottled mutants in the mouse | Q28512192 | ||
| Copper metabolism in mottled mouse mutants. Copper concentrations in tissues during development | Q28513454 | ||
| A study of copper treatment and tissue copper levels in the murine congenital copper deficiency, mottled | Q28593996 | ||
| A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration | Q34263233 | ||
| Therapeutic implications of copper deficiency in Menkes's steely-hair syndrome | Q35150903 | ||
| Neuronal Degeneration in the Brain of the Brindled Mouse—A Light Microscope Study | Q36570076 | ||
| Neuronal degeneration in the brain of the brindled mouse. II. Ultrastructure of neuronal inclusions in the cerebral cortex | Q40271509 | ||
| Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice | Q42022449 | ||
| Menkes's syndrome. Report of a patient treated from 21 days of age with parenteral copper | Q42092423 | ||
| A study of the copper-binding proteins in liver and kidney tissue of neonatal normal and mottled mutant mice | Q42880324 | ||
| Neuronal degeneration in the brain of the brindled mouse. An ultrastructural study of the cerebral cortical neurons | Q48110923 | ||
| Is Menkes syndrome a copper storage disorder? | Q48163567 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 485-487 | |
| P577 | publication date | 1982-09-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | The effect of copper supplementation on the concentration of copper in the brain of the brindled mouse | |
| P478 | volume | 205 |
| Q48387725 | Cerebellar changes of the female mice heterozygous for brindled gene |
| Q41940659 | Comparisons of copper deficiency states in the murine mutants blotchy and brindled. Changes in copper-dependent enzyme activity in 13-day-old mice |
| Q48709204 | Congenital copper deficiency: copper therapy and dopamine-beta-hydroxylase activity in the mottled (brindled) mouse |
| Q73925297 | Early neuroradiologic evidence of degeneration in Menkes' disease |
| Q34272276 | Hepatic metallothionein synthesis in neonatal Mottled-Brindled mutant mice |
| Q48102884 | Life-span and Menkes kinky hair syndrome: report of a 13-year course of this disease |
| Q48621638 | Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease |
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