0000000000240307

AUTHOR

Franziska Hoche

showing 2 related works from this author

Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2)

2013

Aims: Spinocerebellar ataxia type 2 (SCA2) belongs to the CAG repeat or polyglutamine diseases. Along with a large variety of motor, behavioural and neuropsychological symptoms the clinical picture of patients suffering from this autosomal dominantly inherited ataxia may also include deficits of attention, impairments of memory, as well as frontal-executive and visuospatial dysfunctions. As the possible morphological correlates of these cognitive SCA2 deficits are unclear we examined the cholinergic basal forebrain nuclei, which are believed to be crucial for several aspects of normal cognition and may contribute to impairments of cognitive functions under pathological conditions. Methods: …

Medial septal nucleusBasal forebrainHistologyAtaxiabusiness.industrySubstantia innominataAnatomymedicine.diseaseDiagonal band of BrocaPathology and Forensic Medicinemedicine.anatomical_structurenervous systemNeurologyPhysiology (medical)medicineSpinocerebellar ataxiaCholinergicNeurology (clinical)medicine.symptomCholinergic neuronbusinessNeuroscienceNeuropathology and Applied Neurobiology
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Degeneration of the Cerebellum in Huntington's Disease (HD): Possible Relevance for the Clinical Picture and Potential Gateway to Pathological Mechan…

2012

Huntington's disease (HD) is a polyglutamine disease and characterized neuropathologically by degeneration of the striatum and select layers of the neo- and allocortex. In the present study, we performed a systematic investigation of the cerebellum in eight clinically diagnosed and genetically confirmed HD patients. The cerebellum of all HD patients showed a considerable atrophy, as well as a consistent loss of Purkinje cells and nerve cells of the fastigial, globose, emboliform and dentate nuclei. This pathology was obvious already in HD brains assigned Vonsattel grade 2 striatal atrophy and did not correlate with the extent and distribution of striatal atrophy. Therefore, our findings sug…

CerebellumPathologymedicine.medical_specialtyAtaxiaGeneral NeuroscienceNeurodegenerationmedicine.diseasePathology and Forensic MedicinePathogenesisDysarthriamedicine.anatomical_structureAtrophynervous systemHuntington's diseasemedicineCorticobasal degenerationNeurology (clinical)medicine.symptomPsychologyNeuroscienceBrain Pathology
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