Glial cell cytoplasmic inclusions in SCA2 do not express α-synuclein [8]

Journal of Neurology

Volumn 252, Issue 6, 2005, Pages 742-744

  Berciano, José ^a   Ferrer, Isidro ^b  

^a HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

^b UNIVERSITY OF BARCELONA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; MOLECULAR MARKER; NUCLEIC ACID BINDING PROTEIN; SPINOCEREBELLAR ATAXIA 2 PROTEIN; UBIQUITIN; UNCLASSIFIED DRUG;

ATAXIA; CELL INCLUSION; CONFOCAL MICROSCOPY; CONTROLLED STUDY; GLIA CELL; HEREDITARY ATAXIA; HUMAN; HUMAN CELL; HYPOREFLEXIA; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; LETTER; MUSCLE ATROPHY; MYOKYMIA; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ADULT; ALPHA-SYNUCLEIN; CEREBELLAR DISEASES; FLUORESCENT ANTIBODY TECHNIQUE; HUMANS; INCLUSION BODIES; MALE; MICROSCOPY, CONFOCAL; MULTIPLE SYSTEM ATROPHY; NERVE TISSUE PROTEINS; NEUROGLIA; SYNUCLEINS;

EID: 20844458601     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-005-0747-6     Document Type: Letter

References (6)

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3. Gilman S, Sima AAF, Junck L, Kluin KJ, Koeppe RA, Lohman ME, Little R (1996) Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions. Ann Neurol 39: 241-255
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6. Wüllner U, Abele M, Schmitz-Huebsch T, Wilhelm K, Benecke R, Deuschl G, Klockgether T (2004) Probable multiple system atrophy in a German family. J Neurol Neurosurg Psychiatry 75: 924-925