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Network correlates of disease severity in multiple system atrophy

Neurology, 2012-04, Vol.78 (16), p.1237-1244

2012

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Increased number of Purkinje cell dendritic swellings in essential tremor

European journal of neurology, 2012-04, Vol.19 (4), p.625-630

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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Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains

Acta neuropathologica, 2021-03, Vol.141 (3), p.399-413

2021

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Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration

Journal of neuropathology and experimental neurology, 2002-11, Vol.61 (11), p.935-946

2002

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Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in Brain

Science (American Association for the Advancement of Science), 1997-09, Vol.277 (5334), p.1990-1993

1997

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Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

European journal of neurology, 2009-03, Vol.16 (3), p.297-309

2009

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Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis–frontotemporal dementia phenotypes

Journal of neurology, neurosurgery and psychiatry, 2007-07, Vol.78 (7), p.754-756

2007

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Early and Progressive Accumulation of Reactive Microglia in the Huntington Disease Brain

Journal of neuropathology and experimental neurology, 2001-02, Vol.60 (2), p.161-172

2001

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Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease

Neurology, 2008-03, Vol.70 (11), p.887-889

2008

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Rapid Induction of Alzheimer Aβ Amyloid Formation by Zinc

Science (American Association for the Advancement of Science), 1994-09, Vol.265 (5177), p.1464-1467

1994

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Minocycline inhibits caspase-1 and caspase-3 expression and delays mortality in a transgenic mouse model of Huntington disease

Nature medicine, 2000-07, Vol.6 (7), p.797-801

2000

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Huntingtin localization in brains of normal and Huntington's disease patients

Annals of neurology, 1997-10, Vol.42 (4), p.604-612

1997

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CAG repeat number governs the development rate of pathology in Huntington's disease

Annals of neurology, 1997-05, Vol.41 (5), p.689-692

1997

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Memory performance is related to amyloid and tau pathology in the hippocampus

Journal of neurology, neurosurgery and psychiatry, 2009-07, Vol.80 (7), p.715-721

2009

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Huntington Disease

Journal of neuropathology and experimental neurology, 1998-05, Vol.57 (5), p.369-384

1998

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Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

Nature genetics, 1997-12, Vol.17 (4), p.404-410

1997

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Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

Neuron (Cambridge, Mass.), 1995-05, Vol.14 (5), p.1075-1081

1995

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Up-regulation of the lysosomal system in experimental models of neuronal injury: implications for Alzheimer’s disease

Neuroscience, 2000-01, Vol.100 (3), p.663-675

2000

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Inactivation of the Mouse Huntington's Disease Gene Homolog Hdh

Science (American Association for the Advancement of Science), 1995-07, Vol.269 (5222), p.407-410

1995

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DNA strand breaks in Alzheimer's disease

Brain research, 1999-12, Vol.849 (1), p.67-77

1999

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Evidence for a preferential loss of enkephalin immunoreactivity in the external globus pallidus in low grade Huntington's disease using high resolution image analysis

Neuroscience, 1995, Vol.64 (2), p.397-404

1995

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Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis

Human molecular genetics, 2000-09, Vol.9 (14), p.2175-2182

2000

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Neuropathologic findings in essential tremor

Neurology, 2006-06, Vol.66 (11), p.1756-1759

2006

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Axonal Transport of N-terminal Huntingtin Suggests Early Pathology of Corticostriatal Projections in Huntington Disease

Journal of neuropathology and experimental neurology, 1999-02, Vol.58 (2), p.165-173

1999

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Network correlates of disease severity in multiple system atrophy

Increased number of Purkinje cell dendritic swellings in essential tremor

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

Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains

Office of Rare Diseases Neuropathologic Criteria for Corticobasal Degeneration

Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in Brain

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis–frontotemporal dementia phenotypes

Early and Progressive Accumulation of Reactive Microglia in the Huntington Disease Brain

Association between genetic variants in SORL1 and autopsy-confirmed Alzheimer disease

Rapid Induction of Alzheimer Aβ Amyloid Formation by Zinc

Minocycline inhibits caspase-1 and caspase-3 expression and delays mortality in a transgenic mouse model of Huntington disease

Huntingtin localization in brains of normal and Huntington's disease patients

CAG repeat number governs the development rate of pathology in Huntington's disease

Memory performance is related to amyloid and tau pathology in the hippocampus

Huntington Disease

Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion

Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

Up-regulation of the lysosomal system in experimental models of neuronal injury: implications for Alzheimer’s disease

Inactivation of the Mouse Huntington's Disease Gene Homolog Hdh

DNA strand breaks in Alzheimer's disease

Evidence for a preferential loss of enkephalin immunoreactivity in the external globus pallidus in low grade Huntington's disease using high resolution image analysis

Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis

Neuropathologic findings in essential tremor

Axonal Transport of N-terminal Huntingtin Suggests Early Pathology of Corticostriatal Projections in Huntington Disease

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