Globular glial tauopathies (GGT): Consensus recommendations

Acta Neuropathologica

Volumn 126, Issue 4, 2013, Pages 537-544

  Ahmed, Zeshan ^a   Bigio, Eileen H ^b   Budka, Herbert ^c,l   Dickson, Dennis W ^d   Ferrer, Isidro ^e   Ghetti, Bernardino ^f   Giaccone, Giorgio ^g   Hatanpaa, Kimmo J ^h   Holton, Janice L ^a   Josephs, Keith A ⁱ   Powers, James ^j   Spina, Salvatore ^f   Takahashi, Hitoshi ^k   White III, Charles L ^h   Revesz, Tamas ^a   Kovacs, Gabor G ^c  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b NORTHWESTERN UNIVERSITY   (United States)

^c MEDICAL UNIVERSITY OF VIENNA   (Austria)

^d MAYO CLINIC   (United States)

^e HOSPITAL UNIVERSITARI DE BELLVITGE   (Spain)

^f INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^g DEPARTMENT OF NEUROSURGERY   (Italy)

^h University of Texas   (United States)

ⁱ MAYO CLINIC   (United States)

^j UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

^k NIIGATA UNIVERSITY   (Japan)

^l UNIVERSITY HOSPITAL ZURICH   (Switzerland)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASTROCYTE; CELL INCLUSION; CONSENSUS DEVELOPMENT; DISEASE CLASSIFICATION; FRONTOTEMPORAL DEMENTIA; GLIA CELL; GLOBULAR GLIAL TAUOPATHY; HUMAN; MEDICAL TERMINOLOGY; MOTOR NEURON DISEASE; NEUROPATHOLOGY; OLIGODENDROGLIA; PARKINSONISM; PRIORITY JOURNAL; TAUOPATHY;

ASTROCYTES; CONSENSUS; HUMANS; IMMUNOHISTOCHEMISTRY; INCLUSION BODIES; NEURODEGENERATIVE DISEASES; NEUROGLIA; SILVER STAINING; TAU PROTEINS; TAUOPATHIES; TERMINOLOGY AS TOPIC;

EID: 84885484879     PISSN: 00016322     EISSN: 14320533     Source Type: Journal    
DOI: 10.1007/s00401-013-1171-0     Document Type: Article

References (27)

1. Ahmed Z, Doherty KM, Silveira-Moriyama L et al (2011) Globular glial tauopathies (GGT) presenting with motor neuron disease or frontotemporal dementia: an emerging group of 4-repeat tauopathies. Acta Neuropathol 122:415-428
2. Berry RW, Quinn B, Johnson N, Cochran EJ, Ghoshal N, Binder LI (2001) Pathological glial tau accumulations in neurodegenerative disease: review and case report. Neurochem Int 39:469-479
3. Bigio EH, Lipton AM, Yen SH et al (2001) Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia. J Neuropathol Exp Neurol 60:328-341
4. Cairns NJ, Atkinson PF, Hanger DP, Anderton BH, Daniel SE, Lantos PL (1997) Tau protein in the glial cytoplasmic inclusions of multiple system atrophy can be distinguished from abnormal tau in Alzheimer's disease. Neurosci Lett 230:49-52
5. Dickson DW, Hauw JJ, Agid Y, Litvan I (2011) Progressive supranuclear palsy and corticobasal degeneration. In: Dickson DW, Weller RO (eds) Neurodegeneration: The molecular pathology of dementia and movement disorders, 2nd edn. Wiley-Blackwell, Chichester, West Sussex, pp 135-155
6. Ferrer I, Hernandez I, Boada M et al (2003) Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies. Acta Neuropathol 106:419-435
7. Fu YJ, Nishihira Y, Kuroda S et al (2010) Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity. Acta Neuropathol 120:21-32
8. Gallyas F (1971) Silver staining of Alzheimer's neurofibrillary changes by means of physical development. Acta morphol Acad Sci Hung 19:1-8
9. Ghetti B, Wszolek EK, Boeve BF, Spina S, Goedert M (2011) Frontotemporal dementia and Parkinsonism linked to chromosome 17. In: Dickson DW, Weller RO (eds) Neurodegeneration: the molecular pathology of dementia and movement disorders. Wiley-Blackwell, Chichester, West Sussex, pp 110-134
10. Giaccone G, Marcon G, Mangieri M et al (2008) Atypical tauopathy with massive involvement of the white matter. Neuropathol Appl Neurobiol 34:468-472
11. Hayashi S, Toyoshima Y, Hasegawa M et al (2002) Late-onset frontotemporal dementia with a novel exon 1 (Arg5His) tau gene mutation. Ann Neurol 51:525-530
12. Josephs KA, Katsuse O, Beccano-Kelly DA et al (2006) Atypical progressive supranuclear palsy with corticospinal tract degeneration. J Neuropathol Exp Neurol 65:396-405
13. Kovacs GG, Majtenyi K, Spina S et al (2008) White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration. J Neuropathol Exp Neurol 67:963-975
14. Lashley T, Rohrer JD, Bandopadhyay R et al (2011) A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies. Brain 134:2548-2564
15. Mackenzie IR (2007) The neuropathology of FTD associated With ALS. Alzheimer Dis Assoc Disord 21:S44-S49
16. Mackenzie IR, Neumann M, Bigio EH et al (2009) Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathol 117:15-18
17. Mackenzie IR, Neumann M, Bigio EH et al (2010) Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathol 119:1-4
18. Molina JA, Probst A, Villanueva C et al (1998) Primary progressive aphasia with glial cytoplasmic inclusions. Eur Neurol 40:71-77
19. Ozawa T, Paviour D, Quinn NP et al (2004) The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations. Brain 127:2657-2671
20. Piao YS, Tan CF, Iwanaga K et al (2005) Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease. Acta Neuropathol 110:600-609
21. Powers JM, Byrne NP, Ito M et al (2003) A novel leukoencephalopathy associated with tau deposits primarily in white matter glia. Acta Neuropathol 106:181-187
22. Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MR, Ghetti B (1997) Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments. Proc Natl Acad Sci USA 94:4113-4118
23. Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B (1998) Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci USA 95:7737-7741
24. Spina S, Farlow MR, Unverzagt FW et al (2008) The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family. Brain 131:72-89
25. Tolnay M, Braak H (2011) Argyrophilic grain disease. In: Dickson DW, Weller RO (eds) Neurodegeneration: the molecular pathology of dementia and movement disorders, 2nd edn. Wiley-Blackwell, Chichester, West Sussex, pp 165-170
26. Wenning GK, Stefanova N, Jellinger KA, Poewe W, Schlossmacher MG (2008) Multiple system atrophy: a primary oligodendrogliopathy. Ann Neurol 64:239-246
27. Wray S, Saxton M, Anderton BH, Hanger DP (2008) Direct analysis of tau from PSP brain identifies new phosphorylation sites and a major fragment of N-terminally cleaved tau containing four microtubule-binding repeats. J Neurochem 105:2343-2352