U. Rüb

发表

Staging of brain pathology related to sporadic Parkinson’s disease

H. Braak, E. Braak, K. Tredici, 2003, Neurobiology of Aging.

Phases of Aβ-deposition in the human brain and its relevance for the development of AD

H. Braak, U. Rüb, D. Thal, 2002, Neurology.

Stanley Fahn Lecture 2005: The staging procedure for the inclusion body pathology associated with sporadic Parkinson's disease reconsidered

H. Braak, J. Bohl, C. Müller, 2006, Movement disorders : official journal of the Movement Disorder Society.

U. Rüb, D. Thal, G. Waldmann, 2000, Experimental Neurology.

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

H. Braak, K. Tredici, U. Rüb, 2003, Journal of Neural Transmission.

Staging of the intracerebral inclusion body pathology associated with idiopathic Parkinson's disease (preclinical and clinical stages)

Hansjürgen Bratzke, Udo Rüb, H. Braak, 2002, Journal of Neurology.

The intralaminar nuclei assigned to the medial pain system and other components of this system are early and progressively affected by the Alzheimer's disease-related cytoskeletal pathology

H. Braak, K. Tredici, U. Rüb, 2002, Journal of Chemical Neuroanatomy.

Where Does Parkinson Disease Pathology Begin in the Brain?

Udo Rüb, H. Braak, J. Bohl, 2002, Journal of neuropathology and experimental neurology.

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

Hansjürgen Bratzke, Udo Rüb, H. Braak, 2004, Cell and Tissue Research.

Huntington's Disease (HD): Neurodegeneration of Brodmann's Primary Visual Area 17 (BA17)

Wolfgang Eisenmenger, Udo Rüb, Helmut Heinsen, 2015, Brain pathology.

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

L. Grinberg, J. Farfel, R. E. Ferretti, 2009, Neuropathology and applied neurobiology.

[Neuroanatomy of Parkinson disease. Changes in the neuronal cytoskeleton of a few disease-susceptible types of neurons lead to progressive destruction of circumscribed areas in the limbic and motor systems].

H. Braak, E. Braak, U. Rüb, 2000, Der Nervenarzt.

Evaluation of brain ageing: a quantitative longitudinal MRI study over 7 years

R. Deichmann, J. Klein, H. Steinmetz, 2017, European Radiology.

On protein quality control, myofibrillar myopathies, and neurodegeneration

H. Kampinga, U. Rüb, E. Brunt, 2017 .

On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3

W. D. den Dunnen, U. Rüb, J. D. de Vries, 2017, Brain pathology.

Axonal inclusions in spinocerebellar ataxia type 3

H. Paulson, H. Kampinga, W. D. den Dunnen, 2010, Acta Neuropathologica.

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

H. Paulson, C. Broeckhoven, C. van Broeckhoven, 2006, Neuropathology and applied neurobiology.

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

U. Rüb, E. Schwinger, R. D. de Vos, 2006, Journal of Neural Transmission.

Apolipoprotein E co-localizes with newly formed amyloid beta-protein (Abeta) deposits lacking immunoreactivity against N-terminal epitopes of Abeta in a genotype-dependent manner.

H. Braak, U. Rüb, K. Del Tredici, 2005, Acta neuropathologica.

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

H. Braak, E. Braak, U. Rüb, 2000, Acta Neuropathologica.

The p62 antibody reveals various cytoplasmic protein aggregates in spinocerebellar ataxia type 6.

H. Kampinga, W. D. den Dunnen, U. Rüb, 2009, Clinical neuropathology.

Functional neuroanatomy of the human premotor oculomotor brainstem nuclei: insights from postmortem and advanced in vivo imaging studies

H. Braak, U. Rüb, J. Jen, 2008, Experimental Brain Research.

Progressive supranuclear palsy: neuronal and glial cytoskeletal pathology in the higher order processing autonomic nuclei of the lower brainstem

H. Braak, K. Tredici, U. Rüb, 2002, Neuropathology and applied neurobiology.

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

L. Grinberg, J. Farfel, R. Leite, 2017, Neuropathology and applied neurobiology.

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

H. Heinsen, W. D. den Dunnen, U. Rüb, 2009, Neuropathology and applied neurobiology.

Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient

H. Braak, H. Paulson, U. Rüb, 2003, Neuropathology and applied neurobiology.

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

H. Heinsen, U. Rüb, H. Korf, 2013, Journal of the Neurological Sciences.

The Brain of the Aging Baboon: A Nonhuman Primate Model for Neuronal and Glial Tau Pathology

H. Braak, E. Braak, K. Tredici, 2002 .

Widespread Brainstem Neurodegeneration in Huntington's Disease (HD).

U. Rüb, 2015, Advances in anatomy, embryology, and cell biology.

Argyrophilic grain disease is associated with apolipoprotein E ε2 allele

H. Braak, E. Braak, U. Rüb, 1998, Acta Neuropathologica.

Intraneuronal Transport and Defense Mechanisms with Possible Pathogenetic Relevance in Huntington's Disease (HD).

U. Rüb, H. Korf, 2015, Advances in anatomy, embryology, and cell biology.

Nerve cells expressing heat-shock proteins in Parkinson's disease

H. Braak, K. Tredici, U. Rüb, 2001, Acta Neuropathologica.

Argyrophilic grain disease is associated with apolipoprotein E epsilon 2 allele.

H. Braak, E. Braak, U. Rüb, 1998, Acta neuropathologica.

Intranuclear Aggregation of Nonexpanded Ataxin-3 in Marinesco Bodies of the Nonhuman Primate Substantia Nigra

H. Braak, M. Kettner, U. Rüb, 2002, Experimental Neurology.

Pathology associated with sporadic Parkinson's disease--where does it end?

H. Braak, H. Ackermann, H. Bratzke, 2006, Journal of neural transmission. Supplementum.

Abstracts Second Congress of the European Society for Clinical Neuropharmacology

K. Jellinger, L. Iversen, K. Lesch, 1995, Journal of Neural Transmission / General Section JNT.

Pathological Nerve Cell Alterations in Huntington's Disease (HD) and Their Possible Role for the Demise of Nerve Cells.

U. Rüb, H. Korf, 2015, Advances in anatomy, embryology, and cell biology.

Spinocerebellar ataxia 2 (SCA2)

U. Rüb, G. Auburger, I. Lastres-Becker, 2008, The Cerebellum.

Parkinson Phenotype in Aged PINK1-Deficient Mice Is Accompanied by Progressive Mitochondrial Dysfunction in Absence of Neurodegeneration

R. Nussbaum, A. Reichert, A. Kurz, 2009, PloS one.

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

H. Heinsen, J. Vonsattel, W. D. den Dunnen, 2016, Brain pathology.

Elucidation of the Role of the Premotor Oculomotor Brainstem Nuclei in the Pathogenesis of Oculomotor Dysfunctions in Huntington's Disease (HD).

U. Rüb, 2015, Advances in anatomy, embryology, and cell biology.

Huntington's Disease (HD): Degeneration of Select Nuclei, Widespread Occurrence of Neuronal Nuclear and Axonal Inclusions in the Brainstem

H. Paulson, H. Heinsen, J. Vonsattel, 2014, Brain pathology.

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

K. Krakow, H. Steinmetz, Hanns Lochmüller, 2006, Neurology.

The premotor region essential for rapid vertical eye movements shows early involvement in Alzheimer's disease-related cytoskeletal pathology

H. Braak, J. Büttner-Ennever, K. Tredici, 2001, Vision Research.

Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP).

P. Bauer, W. D. den Dunnen, O. Riess, 2009, Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft.

Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult‐onset patient with progressive visual impairments in comparison with an adult‐onset patient without visual impairments

C. Broeckhoven, C. van Broeckhoven, L. Schöls, 2008, Neuropathology and applied neurobiology.

Spinocerebellar Ataxia Type 3 (SCA3): Thalamic Neurodegeneration Occurs Independently from Thalamic Ataxin‐3 Immunopositive Neuronal Intranuclear Inclusions

H. Paulson, H. Heinsen, L. Schöls, 2006, Brain pathology.

Spinocerebellar Ataxia Type 7 (SCA7): First Report of a Systematic Neuropathological Study of the Brain of a Patient with a Very Short Expanded CAG‐Repeat

H. Heinsen, L. Schöls, U. Rüb, 2005, Brain pathology.

Extended pathoanatomical studies point to a consistent affection of the thalamus in spinocerebellar ataxia type 2

H. Braak, L. Schöls, J. Bohl, 2005, Neuropathology and applied neurobiology.

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

G. Reifenberger, H. Braak, K. Tredici, 2003, Brain : a journal of neurology.

The Neuropathological Grading of Huntington's Disease (HD).

J. Vonsattel, U. Rüb, 2015, Advances in anatomy, embryology, and cell biology.

Brain pathology of spinocerebellar ataxias

U. Rüb, H. Korf, E. Brunt, 2012, Acta Neuropathologica.

Spinocerebellar ataxia type 4

U. Rüb, E. Schwinger, C. Zühlke, 2005, Journal of Neurology.

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

John Q. Trojanowski, Georg Auburger, Arun Padmanabhan, 2010, Nature.

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

R. Baloh, N. Salamon, J. Demer, 2006, Neurology.

Irradiation with X-rays phase-advances the molecular clockwork in liver, adrenal gland and pancreas

U. Rüb, F. Rödel, H. Korf, 2015, Chronobiology international.

Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7

Georg Auburger, Thomas Deller, Udo Rüb, 2013, Progress in Neurobiology.

Characterization of human melatonin synthesis using autoptic pineal tissue.

U. Rüb, H. Korf, J. Stehle, 2006, Endocrinology.

The Brainstem Pathologies of Parkinson's Disease and Dementia with Lewy Bodies

Georg Auburger, Udo Rüb, Helmut Heinsen, 2015, Brain pathology.

Two Types of Sporadic Cerebral Amyloid Angiopathy

H. Braak, K. Tredici, U. Rüb, 2002, Journal of neuropathology and experimental neurology.

Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis

D. Geschwind, S. Nelson, R. Baloh, 2004, Science.

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

D. Timmann, H. Heinsen, L. Schöls, 2012, Neuropathology and applied neurobiology.

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

H. Braak, L. Schöls, U. Rüb, 2005, Acta Neuropathologica.

Degeneration of the Cerebellum in Huntington's Disease (HD): Possible Relevance for the Clinical Picture and Potential Gateway to Pathological Mechanisms of the Disease Process

Udo Rüb, Helmut Heinsen, H. Paulson, 2013, Brain pathology.

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

H. Braak, E. Braak, U. Rüb, 2001, Acta Neuropathologica.

Degeneration of Select Motor and Limbic Nuclei of the Thalamus in Huntington's Disease (HD).

U. Rüb, 2015, Advances in anatomy, embryology, and cell biology.

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

L. Schöls, U. Rüb, H. Korf, 2012, The Cerebellum.

Spinocerebellar Ataxia Type 2 (SCA2): Identification of Early Brain Degeneration in One Monozygous Twin in the Initial Disease Stage

T. Klockgether, U. Rüb, H. Korf, 2011, The Cerebellum.

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

U. Rüb, E. Brunt, T. Deller, 2008, Current opinion in neurology.

SCA3: Neurological features, pathogenesis and animal models

Annalisa Pastore, Olaf Riess, Peter Bauer, 2008, The Cerebellum.

Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy

L. Schöls, U. Rüb, R. Vos, 2007, Brain Research Reviews.

Spinocerebellar ataxias types 2 and 3: degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum

H. Braak, L. Schöls, J. Bohl, 2005, Journal of Neural Transmission.

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

H. Braak, L. Schöls, U. Rüb, 2004, Neurology.

Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance

H. Braak, K. Tredici, U. Rüb, 2004, Neuropathology and applied neurobiology.

Involvement of precerebellar nuclei in multiple system atrophy

H. Braak, K. Tredici, U. Rüb, 2003, Neuropathology and applied neurobiology.

Nerve cell loss in the thalamic mediodorsal nucleus in Huntington’s disease

H. Heinsen, C. Schmitz, U. Rüb, 1999, Acta Neuropathologica.

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

L. Schöls, H. J. Schelhaas, W. D. den Dunnen, 2009, Neuropathology and applied neurobiology.

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

R. Nitrini, L. Grinberg, J. Farfel, 2009, Neuropathology and applied neurobiology.

Anatomically based guidelines for systematic investigation of the central somatosensory system and their application to a spinocerebellar ataxia type 2 (SCA2) patient

G. Reifenberger, H. Braak, K. Tredici, 2003, Neuropathology and applied neurobiology.

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

H. Braak, H. Paulson, U. Rüb, 2002, Brain : a journal of neurology.

The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado–Joseph disease)

H. Braak, U. Rüb, C. Schultz, 2003, Journal of Chemical Neuroanatomy.

Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado–Joseph disease)

H. Braak, K. Tredici, U. Rüb, 2002, Brain Research.

Mapping local hippocampal changes in Alzheimer's disease and normal ageing with MRI at 3 Tesla.

Rossana Ganzola, Carlo Caltagirone, Alberto Beltramello, 2008, Brain : a journal of neurology.

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

H. Kampinga, W. D. den Dunnen, H. Boddeke, 2012, Neuropathology and applied neurobiology.

Cognitive decline correlates with neuropathological stage in Parkinson's disease

H. Braak, K. Tredici, U. Rüb, 2006, Journal of the Neurological Sciences.

Cognitive status correlates with neuropathologic stage in Parkinson disease

H. Braak, K. Tredici, U. Rüb, 2005, Neurology.

Atxn2-CAG100-knock-in affects mouse lifespan and vestibulo-cerebellar function via neural disconnection

C. D. De Zeeuw, L. Bosman, M. Schonewille, 2018, bioRxiv.

ATXN2-CAG42 Sequesters PABPC1 into Insolubility and Induces FBXW8 in Cerebellum of Old Ataxic Knock-In Mice

U. Rüb, C. Seifried, G. Auburger, 2012, PLoS genetics.

Subcortical neurodegeneration in chorea: Similarities and differences between chorea-acanthocytosis and Huntington's disease.

L. Grinberg, A. Danek, H. Heinsen, 2018, Parkinsonism & related disorders.

Apolipoprotein E co-localizes with newly formed amyloid β-protein (Aβ) deposits lacking immunoreactivity against N-terminal epitopes of Aβ in a genotype-dependent manner

H. Braak, K. Tredici, U. Rüb, 2005, Acta Neuropathologica.

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

H. Braak, E. Braak, U. Rüb, 2001, Neurology.

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

H. Braak, E. Braak, U. Rüb, 2000 .

The evolution of Alzheimer's disease‐related cytoskeletal pathology in the human raphe nuclei

H. Braak, E. Braak, K. Tredici, 2000, Neuropathology and applied neurobiology.

Vulnerability of cortical neurons to Alzheimer's and Parkinson's diseases.

Udo Rüb, H. Braak, U. Rüb, 2006, Journal of Alzheimer's disease : JAD.

Sequence of Abeta-protein deposition in the human medial temporal lobe.

H. Braak, E. Braak, U. Rüb, 2000, Journal of neuropathology and experimental neurology.

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

Udo Rüb, H. Braak, K. Tredici, 2004, Neurobiology of Aging.

H. Braak, E. Braak, U. Rüb, 2000, Neurobiology of Aging.

Progression of neurofibrillary changes and PHF-τ in end-stage Alzheimer’s disease is different from plaque and cortical microglial pathology

T. Arendt, U. Rüb, D. Thal, 1998, Neurobiology of Aging.

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

H. Kampinga, U. Rüb, H. Korf, 2016, Neuropathology and applied neurobiology.

The Neuropathology of Huntington’s Disease: Classical Findings, Recent Developments and Correlation to Functional Neuroanatomy

H. Heinsen, J. Vonsattel, U. Rüb, 2015, Advances in Anatomy, Embryology and Cell Biology.

The Cerebral Cortex in Huntington's Disease (HD).

H. Heinsen, U. Rüb, 2015, Advances in anatomy, embryology, and cell biology.

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

L. Grinberg, A. Danek, H. Heinsen, 2018, Neuropathology and Applied Neurobiology.

Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: A voxel-based morphometry study

Carsten Lukas, Boris Suchan, Gebhard Schmid, 2006, Neuroscience Letters.

SCA 3 : Neurological features , pathogenesis and animal models

A. Pastore, P. Bauer, L. Schöls, 2022 .

Quantitative mapping of T1 and T2* discloses nigral and brainstem pathology in early Parkinson's disease

Ralf Deichmann, Simon Baudrexel, Carola Seifried, 2010, NeuroImage.

The autonomic higher order processing nuclei of the lower brain stem are among the early targets of the Alzheimer's disease-related cytoskeletal pathology

H. Braak, E. Braak, K. Tredici, 2001, Acta Neuropathologica.

Neuroanatomical characteristics of the human pre-Bötzinger complex and its involvement in neurodegenerative brainstem diseases.

Thomas Deller, Udo Rüb, U. Rüb, 2011, Brain : a journal of neurology.

Relationship of apolipoprotein E and age at onset to Parkinson disease neuropathology.

H. Braak, H. Bickeböller, U. Rüb, 2006, Journal of neuropathology and experimental neurology.

Cognitive function in multiple system atrophy of the cerebellar type

I. Daum, U. Rüb, K. Bürk, 2006, Movement disorders : official journal of the Movement Disorder Society.

First appraisal of brain pathology owing to A30P mutant alpha‐synuclein

R. Krüger, L. Schöls, Z. Wszolek, 2010, Annals of neurology.

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

H. Kampinga, W. D. den Dunnen, U. Rüb, 2012, Neuropathology and applied neurobiology.

Parkinson’s disease: the thalamic components of the limbic loop are severely impaired by α-synuclein immunopositive inclusion body pathology

H. Braak, K. Tredici, U. Rüb, 2002, Neurobiology of Aging.

Parkinson’s disease: affection of brain stem nuclei controlling premotor and motor neurons of the somatomotor system

H. Braak, E. Braak, U. Rüb, 2000, Acta Neuropathologica.

Longitudinal changes of cortical microstructure in Parkinson's disease assessed with T1 relaxometry

Simon Baudrexel, Johannes C. Klein, Ralf Deichmann, 2016, NeuroImage: Clinical.

RNA biomarkers in prodromal PARK 4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson ' s disease

E. Schröck, W. Oertel, H. Steinmetz, 2018 .

Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease

E. Schröck, W. Oertel, H. Steinmetz, 2017, Disease Models & Mechanisms.

No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra.

L. Schöls, W. D. den Dunnen, U. Rüb, 2015, Brain : a journal of neurology.

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

C. Broeckhoven, C. van Broeckhoven, L. Schöls, 2008, Neuropathology and applied neurobiology.

Potentiation of neurotoxicity in double-mutant mice with Pink1 ablation and A53T-SNCA overexpression

J. Roeper, U. Rüb, G. Auburger, 2014, Human molecular genetics.

Pink1 ablation and A53T-SNCA overexpression

J. Roeper, U. Rüb, G. Auburger, 2014 .

Alzheimer's Disease: Characterization of the Brain Sites of the Initial Tau Cytoskeletal Pathology Will Improve the Success of Novel Immunological Anti-Tau Treatment Approaches.

H. Heinsen, U. Rüb, H. Korf, 2017, Journal of Alzheimer's disease : JAD.

Precortical Phase of Alzheimer's Disease (AD)‐Related Tau Cytoskeletal Pathology

Udo Rüb, Helmut Heinsen, L. Grinberg, 2016, Brain pathology.

Consistent and Widespread Degeneration of the Cerebellum in Huntington's Disease (HD).

U. Rüb, H. Korf, 2015, Advances in anatomy, embryology, and cell biology.

Sequence of A b-Protein Deposition in the Human Medial Temporal Lobe

H. Braak, E. Braak, K. Tredici, 2000 .

Early involvement of the tegmentopontine reticular nucleus during the evolution of Alzheimer’s disease-related cytoskeletal pathology

H. Braak, K. Tredici, U. Rüb, 2001, Brain Research.

The Brainstem Tau Cytoskeletal Pathology of Alzheimer's Disease: A Brief Historical Overview and Description of its Anatomical Distribution Pattern, Evolutional Features, Pathogenetic and Clinical Relevance.

Udo Rüb, Helmut Heinsen, H. Heinsen, 2016, Current Alzheimer research.

Hierarchical Distribution of the Tau Cytoskeletal Pathology in the Thalamus of Alzheimer's Disease Patients.

H. Heinsen, W. D. den Dunnen, U. Rüb, 2015, Journal of Alzheimer's disease : JAD.

Response to Fernagut et al.: The ambiguous nucleus ambiguus

U. Rüb, T. Deller, S. Schwarzacher, 2012 .

Involvement of the cerebellum in Parkinson disease and dementia with Lewy bodies

R. Krüger, L. Schöls, W. D. den Dunnen, 2017, Annals of neurology.

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

H. Bickeböller, U. Rüb, D. Thal, 2010, Journal of neuropathology and experimental neurology.

Nerve cell loss in the thalamic centromedian-parafascicular complex in patients with Huntington’s disease

Wolfgang Eisenmenger, Udo Rüb, Helmut Heinsen, 2009, Acta Neuropathologica.

On protein quality control, myofibrillar myopathies, and neurodegeneration

H. Kampinga, U. Rüb, E. Brunt, 2017 .

Nerve cell loss in the thalamic mediodorsal nucleus in Huntington’s disease. II. Optimization of a stereological estimation procedure

H. Heinsen, C. Schmitz, U. Rüb, 1999, Acta Neuropathologica.

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

H. Kampinga, U. Rüb, M. Meister, 2012, Neuropathology and applied neurobiology.

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

L. Schöls, U. Rüb, H. Korf, 2011, The Cerebellum.

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

H. Braak, H. Paulson, U. Rüb, 2002, Brain : a journal of neurology.

Variability in the human entorhinal region may confound neuropsychiatric diagnoses.

U. Rüb, W. Eisenmenger, H. Heinsen, 1996, Acta anatomica.

On protein quality control, myofibrillar myopathies, and neurodegeneration

H. Kampinga, U. Rüb, E. Brunt, 2017 .