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S5‐01‐04: Hereditary diffuse leukoencephalopathy with axonal spheroids
Author(s) -
Wszolek Zbigniew K.
Publication year - 2009
Publication title -
alzheimer's and dementia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.713
H-Index - 118
eISSN - 1552-5279
pISSN - 1552-5260
DOI - 10.1016/j.jalz.2009.05.573
Subject(s) - medicine , leukodystrophy , leukoencephalopathy , pathological , pathology , parkinsonism , dementia , frontotemporal dementia , disease , pediatrics
findings the term FTLD-U has become obsolete and a revised nomenclature on FTLD was recently recommended. FTLD with tau or TDP-43 pathology are renamed as FTLD-tau and FTLD-TDP, respectively, while FTLD cases with inclusions that can only be demonstrated by immunohistochemistry against proteins of the ubiquitin proteasome system (UPS) are designated as FTLD-UPS until the ubiquitinated protein(s) in these conditions will be identified.