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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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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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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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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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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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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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Cognitive status correlates with neuropathologic stage in Parkinson disease

Neurology, 2005-04, Vol.64 (8), p.1404

2005

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

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

2006

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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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Evolution of Alzheimer's disease-related cytoskeletal changes in the basal nucleus of Meynert

Acta neuropathologica, 2000-09, Vol.100 (3), p.259-269

2000

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Involvement of precerebellar nuclei in multiple system atrophy

Neuropathology and applied neurobiology, 2003-02, Vol.29 (1), p.60-76

2003

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Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance

Brain (London, England : 1878), 2003-10, Vol.126 (10), p.2257-2272

2003

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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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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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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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Spinocerebellar ataxia type 3 (Machado–Joseph disease): severe destruction of the lateral reticular nucleus

Brain (London, England : 1878), 2002-09, Vol.125 (9), p.2115-2124

2002

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Sequence of Aβ-Protein Deposition in the Human Medial Temporal Lobe

Journal of neuropathology and experimental neurology, 2000-08, Vol.59 (8), p.733-748

2000

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Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3

Neurology, 2004-10, Vol.63 (7), p.1258

2004

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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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Gender and age modify the association between APOE and AD-related neuropathology

Neurology, 2001-06, Vol.56 (12), p.1696

2001

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Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2)

Acta neuropathologica, 2005-06, Vol.109 (6), p.617-631

2005

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α-Synuclein immunopositive Parkinson's disease-related inclusion bodies in lower brain stem nuclei

Acta neuropathologica, 2001-03, Vol.101 (3), p.195-201

2001

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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

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

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

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

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

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

Cognitive status correlates with neuropathologic stage in Parkinson disease

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

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

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

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

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

Evolution of Alzheimer's disease-related cytoskeletal changes in the basal nucleus of Meynert

Involvement of precerebellar nuclei in multiple system atrophy

Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance

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

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

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

Spinocerebellar ataxia type 3 (Machado–Joseph disease): severe destruction of the lateral reticular nucleus

Sequence of Aβ-Protein Deposition in the Human Medial Temporal Lobe

Damage to the reticulotegmental nucleus of the pons in spinocerebellar ataxia type 1, 2, and 3

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

Gender and age modify the association between APOE and AD-related neuropathology

Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2)

α-Synuclein immunopositive Parkinson's disease-related inclusion bodies in lower brain stem nuclei

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