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Huntington's disease (HD): the neuropathology of a multisystem neurodegenerative disorder of the human brain

Brain pathology (Zurich, Switzerland), 2016-11, Vol.26 (6), p.726-740

2016

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The dorsal raphe nucleus shows phospho-tau neurofibrillary changes before the transentorhinal region in Alzheimer's disease. A precocious onset?

Neuropathology and applied neurobiology, 2009-08, Vol.35 (4), p.406-416

2009

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Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation

Neuropathology and applied neurobiology, 2016-02, Vol.42 (2), p.153-166

2016

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The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases

Neuropathology and applied neurobiology, 2012-02, Vol.38 (1), p.39-53

2012

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Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights

Neuropathology and applied neurobiology, 2012-12, Vol.38 (7), p.665-680

2012

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Cellular protein quality control and the evolution of aggregates in spinocerebellar ataxia type 3 (SCA3)

Neuropathology and applied neurobiology, 2012-10, Vol.38 (6), p.548-558

2012

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

Neuropathology and applied neurobiology, 2013-10, Vol.39 (6), p.634-643

2013

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Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2)

Neurology, 2006-12, Vol.67 (11), p.1966

2006

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Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites

Neuropathology and applied neurobiology, 2009-10, Vol.35 (5), p.515-527

2009

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Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7

Neuropathology and applied neurobiology, 2006-12, Vol.32 (6), p.635-649

2006

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Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7)

Neuropathology and applied neurobiology, 2008-10, Vol.34 (5), p.479-491

2008

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The human premotor oculomotor brainstem system - can it help to understand oculomotor symptoms in Huntington's disease?

Neuropathology and applied neurobiology, 2009-02, Vol.35 (1), p.4-15

2009

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New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease)

Current opinion in neurology, 2008-04, Vol.21 (2), p.111-116

2008

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Stages in the development of Parkinson's disease-related pathology

Cell and tissue research, 2004-10, Vol.318 (1), p.121-134

2004

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Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration

Journal of Neural Transmission, 2006-07, Vol.113 (7), p.829-843

2006

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Quantifying the accretion of hyperphosphorylated tau in the locus coeruleus and dorsal raphe nucleus: the pathological building blocks of early Alzheimer's disease

Neuropathology and applied neurobiology, 2017-08, Vol.43 (5), p.393-408

2017

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Staging of brain pathology related to sporadic Parkinson’s disease

Neurobiology of aging, 2003-03, Vol.24 (2), p.197-211

2003

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Idiopathic Parkinson's disease: possible routes by which vulnerable neuronal types may be subject to neuroinvasion by an unknown pathogen

Journal of Neural Transmission, 2003-05, Vol.110 (5), p.517-536

2003

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Inverse Relationship Between Cerebrovascular Lesions and Severity of Lewy Body Pathology in Patients With Lewy Body Diseases

Journal of neuropathology and experimental neurology, 2010-05, Vol.69 (5), p.442-448

2010

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Pathoarchitectonics of the cerebral cortex in chorea‐acanthocytosis and Huntington's disease

Neuropathology and applied neurobiology, 2019-04, Vol.45 (3), p.230-243

2019

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Pathoanatomy of Cerebellar Degeneration in Spinocerebellar Ataxia Type 2 (SCA2) and Type 3 (SCA3)

Cerebellum (London, England), 2012-09, Vol.11 (3), p.749-760

2012

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Genetic association of argyrophilic grain disease with polymorphisms in alpha-2 macroglobulin and low-density lipoprotein receptor-related protein genes

Neuropathology and applied neurobiology, 2002-08, Vol.28 (4), p.308-313

2002

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First patho-anatomical investigation of the brain of a SCA19 patient

Neuropathology and applied neurobiology, 2014-08, Vol.40 (5), p.640-644

2014

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Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations

Neurology, 2006-08, Vol.67 (3), p.519

2006

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High prevalence of thorn-shaped astrocytes in the aged human medial temporal lobe

Neurobiology of aging, 2004-03, Vol.25 (3), p.397-405

2004

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Huntington's disease (HD): the neuropathology of a multisystem neurodegenerative disorder of the human brain

The dorsal raphe nucleus shows phospho-tau neurofibrillary changes before the transentorhinal region in Alzheimer's disease. A precocious onset?

Polyglutamine aggregation in Huntington's disease and spinocerebellar ataxia type 3: similar mechanisms in aggregate formation

The HSPB8-BAG3 chaperone complex is upregulated in astrocytes in the human brain affected by protein aggregation diseases

Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights

Cellular protein quality control and the evolution of aggregates in spinocerebellar ataxia type 3 (SCA3)

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

Stages of sleep pathology in spinocerebellar ataxia type 2 (SCA2)

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7

Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7)

The human premotor oculomotor brainstem system - can it help to understand oculomotor symptoms in Huntington's disease?

New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease)

Stages in the development of Parkinson's disease-related pathology

Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration

Quantifying the accretion of hyperphosphorylated tau in the locus coeruleus and dorsal raphe nucleus: the pathological building blocks of early Alzheimer's disease

Staging of brain pathology related to sporadic Parkinson’s disease

Idiopathic Parkinson's disease: possible routes by which vulnerable neuronal types may be subject to neuroinvasion by an unknown pathogen

Inverse Relationship Between Cerebrovascular Lesions and Severity of Lewy Body Pathology in Patients With Lewy Body Diseases

Pathoarchitectonics of the cerebral cortex in chorea‐acanthocytosis and Huntington's disease

Pathoanatomy of Cerebellar Degeneration in Spinocerebellar Ataxia Type 2 (SCA2) and Type 3 (SCA3)

Genetic association of argyrophilic grain disease with polymorphisms in alpha-2 macroglobulin and low-density lipoprotein receptor-related protein genes

First patho-anatomical investigation of the brain of a SCA19 patient

Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutations

High prevalence of thorn-shaped astrocytes in the aged human medial temporal lobe

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