Difference between revisions of "Neurodegenerative diseases"

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(→‎Overview: update)
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{{familytree  | | | | | | | A01 | | | | | | | | A01=Neurodegenerative<br>disorders}}
{{familytree  | | | | | | | A01 | | | | | | | | A01=Neurodegenerative<br>disorders}}
{{familytree  | |,|-|-|-|v|-|^|-|v|-|-|-|v|-|-|-|.| | |}}
{{familytree  | |,|-|-|-|v|-|^|-|v|-|-|-|v|-|-|-|.| | |}}
{{familytree  | B01 | | B02 | | B03 | | B04 | | B05 || B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43|B05=FUS}}
{{familytree  | B01 | | B02 | | B03 | | B04 | | B05 || B01=Amyloidoses|B02=Tauopathies|B03=α-synucleinopathies|B04=TDP-43|B05=FUS/EWS/TAF15}}
{{familytree/end}}
{{familytree/end}}


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*Frontotemporal lobar degeneration with TDP-43 (FTLD-TDP).
*Frontotemporal lobar degeneration with TDP-43 (FTLD-TDP).


FUS proteinopathies:
FET proteinopathies:
*Basophilic inclusion body disease (BIBD).
*Basophilic inclusion body disease (BIBD).
*Neuronal intermediate filament inclusion disease (NIFID).
*Neuronal intermediate filament inclusion disease (NIFID).
*Frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U).
*Atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions (atypical FTLD-U).


Prionopathies:
Prionopathies:
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