Quantum redactiones paginae "Sclerosis lateralis amyotrophica" differant

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Neuronibus motoriorum degeneratis et superioribus et inferioribus [[symptoma]]ta ac signa [[musculus|musculorum]] et tenuitas (atrophia) et infirmitas corporis apparent. Cum initium non rare obscure esset, in morbi cursu symptomata muscularia progrediantur. Adhuc omnibus rationibus infrenata, postremo morbus quamcumque gubernationem motuum voluntariam affert, quamquam et [[vesica urinaria|vesicae]] et tractūs gastrointestinalis et [[musculus externus bulbi oculi|musculorum bulbi oculi externorum]] gubernatio saepe usque ad extremum intacta restabit<ref>{{cite journal |authors=Hobson E. V., McDermott C. J. |title=Supportive and symptomatic management of amyotrophic lateral sclerosis |journal=Nat Review of Neurology |year=2016 |volume=12 |pages=526-38 |url=https://www.ncbi.nlm.nih.gov/pubmed/27514291}.</ref>.
 
Nuper sclerosem lateralem amyotrophicam etiam symptomata obstringere prospectatum est. Symptomata psychiatrica ut [[schizophrenia]]e vel [[perturbatio affectionis mentis|mali affectionis]] iam descripta sunt<ref>{{cite journal |authors=Zucchi E., Ticozzi N., Mandrioli J. |title=Psychiatric Symptoms in Amyotrophic Lateral Sclerosis: Beyond a Motor Neuron Disorder |journal=Frontiers in neuroscience |year=2019 |volume=13 |pages=175 |url=https://www.ncbi.nlm.nih.gov/pubmed/30914912}}</ref>. Porro nexus cum [[degeneratio lobularis frontotemporalis|degeneratione lobulari frontotemporali]] suspicatus est.
 
== Neuropathologia ==