Template:Central nervous system disease: Difference between revisions
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| list2 = [[Huntington's disease]] - [[Spinocerebellar ataxia]] ([[Friedreich's ataxia]], [[Ataxia telangiectasia]], [[Hereditary spastic paraplegia]])<BR> |
| list2 = [[Huntington's disease]] - [[Spinocerebellar ataxia]] ([[Friedreich's ataxia]], [[Ataxia telangiectasia]], [[Hereditary spastic paraplegia]])<BR> |
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[[Spinal muscular atrophy]]: [[Werdnig-Hoffman disease]] - [[Kugelberg-Welander disease]] - [[Fazio Londe syndrome]] - [[Motor neurone disease|MND]] ([[Amyotrophic lateral sclerosis |
[[Spinal muscular atrophy]]: [[Werdnig-Hoffman disease]] - [[Kugelberg-Welander disease]] - [[Fazio Londe syndrome]] - [[Motor neurone disease|MND]] ([[Amyotrophic lateral sclerosis]] (ALS), [[Progressive muscular atrophy]] (PMA), [[Progressive bulbar palsy|Progressive bulbar]], [[Pseudobulbar palsy|Pseudobulbar]], [[Primary lateral sclerosis|PLS]]) |
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| group3 = [[Extrapyramidal]] and movement disorders |
| group3 = [[Extrapyramidal]] and movement disorders |
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