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Papp–Lantos inclusions and the pathogenesis of multiple system atrophy: an update

Acta neuropathologica, 2010-06, Vol.119 (6), p.657-667

2010

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Overlap between neurodegenerative disorders

Neuropathology, 2005-06, Vol.25 (2), p.111-124

2005

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Obituary of Mátyás Papp (1927–2019)

Brain pathology (Zurich, Switzerland), 2019-07, Vol.29 (4), p.583-583

2019

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What determines the molecular composition of abnormal protein aggregates in neurodegenerative disease?

Neuropathology, 2008-08, Vol.28 (4), p.351-365

2008

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A quantitative study of the pathological changes in white matter in multiple system atrophy

Neuropathology, 2007-06, Vol.27 (3), p.221-227

2007

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Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. [Addendum: Oct 2, 1997, v. 389 (6650), p. 526.]

Nature (London), 1995-12, Vol.378 (6559), p.779-783

1995

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The Definition of Multiple System Atrophy: A Review of Recent Developments

Journal of neuropathology and experimental neurology, 1998-12, Vol.57 (12), p.1099-1111

LANTOS, PETER L

1998

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Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies

British journal of psychiatry, 1999-01, Vol.174 (1), p.45-50

1999

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Olfactory bulb in multiple system atrophy

Movement disorders, 2003-08, Vol.18 (8), p.938-942

2003

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Species-Barrier-Independent Prion Replication in Apparently Resistant Species

Proceedings of the National Academy of Sciences - PNAS, 2000-08, Vol.97 (18), p.10248-10253

2000

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Olfactory centres in Alzheimer's disease: olfactory bulb is involved in early Braak's stages

Neuroreport, 2001-02, Vol.12 (2), p.285-288

2001

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Structural and functional changes in skeletal muscle in anorexia nervosa

Acta neuropathologica, 1998-06, Vol.95 (6), p.632-640

1998

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Decrease and Structural Modifications of Phosphatidylethanolamine Plasmalogen in the Brain with Alzheimer Disease

Journal of neuropathology and experimental neurology, 1999-07, Vol.58 (7), p.740-747

1999

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Neuronal loss and neurofibrillary degeneration in the hippocampal cortex in late‐onset sporadic Alzheimer's disease

Psychiatry and clinical neurosciences, 2000-10, Vol.54 (5), p.523-529

2000

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Are pathological lesions in neurodegenerative disorders the cause or the effect of the degeneration?

Neuropathology, 2002-09, Vol.22 (3), p.133-146

2002

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A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies

Annals of neurology, 2000-12, Vol.48 (6), p.939-943

2000

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Pick's disease is associated with mutations in the tau gene

Annals of neurology, 2000-12, Vol.48 (6), p.859-867

2000

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Glyceraldehyde 3-phosphate dehydrogenase and endothelin-1 immunoreactivity is associated with cerebral white matter damage in dentatorubral-pallidoluysian atrophy

Neuropathology, 2003-03, Vol.23 (1), p.36-43

2003

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Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions

Neuroscience letters, 2003-05, Vol.341 (3), p.177-180

2003

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Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease

Neuropathology, 2001-03, Vol.21 (1), p.19-24

2001

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Spatial correlations between the vacuolation, prion protein deposits, and surviving neurons in the cerebral cortex in sporadic Creutzfeldt-Jakob disease

Neuropathology, 2001-12, Vol.21 (4), p.266-271

2001

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A quantitative study of the pathological changes in cortical neurons in sporadic Creutzfeldt-Jakob disease

Neuropathology, 2003-09, Vol.23 (3), p.181-187

2003

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Cerebellar pathology in sporadic and familial Alzheimer's disease including APP 717 (Val→Ile) mutation cases: A morphometric investigation

Journal of the neurological sciences, 1997-08, Vol.149 (2), p.177-184

1997

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Expression of Cellular Prion Protein in the Frontal and Occipital Lobe in Alzheimer's Disease, Diffuse Lewy Body Disease, and in Normal Brain: An Immunohistochemical Study

The journal of histochemistry and cytochemistry, 2005-08, Vol.53 (8), p.929-940

2005

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Neuropathological Diagnostic Criteria for Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

Brain pathology (Zurich, Switzerland), 1995-10, Vol.5 (4), p.459-466

1995

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Papp–Lantos inclusions and the pathogenesis of multiple system atrophy: an update

Overlap between neurodegenerative disorders

Obituary of Mátyás Papp (1927–2019)

What determines the molecular composition of abnormal protein aggregates in neurodegenerative disease?

A quantitative study of the pathological changes in white matter in multiple system atrophy

Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. [Addendum: Oct 2, 1997, v. 389 (6650), p. 526.]

The Definition of Multiple System Atrophy: A Review of Recent Developments

Validity of current clinical criteria for Alzheimer's disease, vascular dementia and dementia with Lewy bodies

Olfactory bulb in multiple system atrophy

Species-Barrier-Independent Prion Replication in Apparently Resistant Species

Olfactory centres in Alzheimer's disease: olfactory bulb is involved in early Braak's stages

Structural and functional changes in skeletal muscle in anorexia nervosa

Decrease and Structural Modifications of Phosphatidylethanolamine Plasmalogen in the Brain with Alzheimer Disease

Neuronal loss and neurofibrillary degeneration in the hippocampal cortex in late‐onset sporadic Alzheimer's disease

Are pathological lesions in neurodegenerative disorders the cause or the effect of the degeneration?

A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies

Pick's disease is associated with mutations in the tau gene

Glyceraldehyde 3-phosphate dehydrogenase and endothelin-1 immunoreactivity is associated with cerebral white matter damage in dentatorubral-pallidoluysian atrophy

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions

Spatial pattern of prion protein deposits in patients with sporadic Creutzfeldt-Jakob disease

Spatial correlations between the vacuolation, prion protein deposits, and surviving neurons in the cerebral cortex in sporadic Creutzfeldt-Jakob disease

A quantitative study of the pathological changes in cortical neurons in sporadic Creutzfeldt-Jakob disease

Cerebellar pathology in sporadic and familial Alzheimer's disease including APP 717 (Val→Ile) mutation cases: A morphometric investigation

Expression of Cellular Prion Protein in the Frontal and Occipital Lobe in Alzheimer's Disease, Diffuse Lewy Body Disease, and in Normal Brain: An Immunohistochemical Study

Neuropathological Diagnostic Criteria for Creutzfeldt-Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

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