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ALS/MND: the spectrum of clinical and pathological phenotypes

Journal of the neurological sciences, 2015-10, Vol.357, p.e507-e507

Ludolph, A.C

2015

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Formation and characterisation of neuromuscular junctions between hiPSC derived motoneurons and myotubes

Stem cell research, 2015-09, Vol.15 (2), p.328-336

2015

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EPV 3. Regional microstructural impairment is associated with characteristic altered oculomotor performance in Parkinsonian syndromes

Clinical neurophysiology, 2016-09, Vol.127 (9), p.e223-e224

2016

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ID 221 – Disturbed eye movement control in Parkinson’s disease correlates with intrinsic functional connectivity within cortical networks

Clinical neurophysiology, 2016-03, Vol.127 (3), p.e72-e72

2016

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P18. Pattern of ‘resting-state’ functional hyperconnectivity in Amyotrophic lateral sclerosis reflects neuropathological disease stages

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e95-e95

2015

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P19. The brain’s default mode is associated with executive oculomotor deficits in Parkinson’s disease

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e95-e96

2015

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V13. Alterations of ‘resting-state’ functional connectivity in cognitively unimpaired and impaired patients with Parkinson’s disease

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e71-e72

2015

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EPV 2. Spreading patterns of behavioral variant frontotemporal dementia: Analysis of longitudinal in vivo diffusion tensor imaging data

Clinical neurophysiology, 2016-09, Vol.127 (9), p.e223-e223

2016

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EP 50. Correlation between oculomotor changes and atlas-based volumetry in patients with different neurodegenerative Parkinson syndromes

Clinical neurophysiology, 2016-09, Vol.127 (9), p.e259-e260

2016

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FV 14. Longitudinal recordings of eye movements confirm the model of sequential oculomotor alterations in amyotrophic lateral sclerosis consistent with the neuropathological staging scheme

Clinical neurophysiology, 2016-09, Vol.127 (9), p.e217-e218

2016

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Stages of oculomotor dysfunctions confirms the model of axonal spread of pTDP-43 pathology in amyotrophic lateral sclerosis

Clinical neurophysiology, 2016-03, Vol.127 (3), p.e34-e34

2016

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ID 231 – Multicentric structural connectome analysis in 240 patients with amyotrophic lateral sclerosis

Clinical neurophysiology, 2016-03, Vol.127 (3), p.e76-e77

2016

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V42. De novo mutations in the FUS gene are a frequent cause of sporadic ALS in very young patients

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e87-e87

2015

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Comparative phenotypical differences of Amyotrophic Lateral Sclerosis (ALS) in Germany and China

Journal of the neurological sciences, 2015-10, Vol.357, p.e229-e229

2015

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P 33. Investigation of microstructural alterations of ALS-specific tracts in asymptomatic ALS-mutation carriers

Clinical neurophysiology, 2021-08, Vol.132 (8), p.e15-e15

2021

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P-46 The effect of bevacizumab on cerebral microstructures in high-grade glioma

Clinical neurophysiology, 2023-04, Vol.148, p.e29-e29

2023

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P-39 Hypothalamus volumetry in idiopathic intracranial hypertension: A controlled 3-D MRI study with BMI matching

Clinical neurophysiology, 2023-04, Vol.148, p.e26-e26

2023

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Frontiers of amyotrophic lateral sclerosis cognitive assessment: The use of Eye-tracking and Brain Computer Interface in the eBrain project

Journal of the neurological sciences, 2013-10, Vol.333, p.e457-e457

2013

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Neurodevelopmental and neurodegenerative diseases – Is there a pathophysiological link? Attention-deficit/hyperactivity disorder and amyotrophic lateral sclerosis as examples

Medical hypotheses, 2008-01, Vol.70 (6), p.1133-1138

2008

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P 9 A multi-modal in vivo staging approach to amyotrophic lateral sclerosis

Clinical neurophysiology, 2022-05, Vol.137, p.e19-e20

2022

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FV 3. Diagnostic value of oculomotor parameters in progressive supranuclear palsy: a monocentric study in 100 patients

Clinical neurophysiology, 2021-08, Vol.132 (8), p.e29-e30

2021

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Alcohol withdrawal syndrome: mechanisms, manifestations, and management

Acta neurologica Scandinavica, 2017-01, Vol.135 (1), p.4-16

2017

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P-109 Association of disease severity and sequential alterations in diffusion metrics in amyotrophic lateral sclerosis

Clinical neurophysiology, 2023-04, Vol.148, p.e57-e57

2023

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Erweiterte therapeutische Strategien bei neurologischen Erkrankungen: Gegenwart und Perspektiven

Nervenarzt, 2011-08, Vol.82 (8), p.955-956

2011

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FV 5. MRI-based texture analysis of the corpus callosum in progressive supranuclear palsy

Clinical neurophysiology, 2021-08, Vol.132 (8), p.e31-e31

2021

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ALS/MND: the spectrum of clinical and pathological phenotypes

Formation and characterisation of neuromuscular junctions between hiPSC derived motoneurons and myotubes

EPV 3. Regional microstructural impairment is associated with characteristic altered oculomotor performance in Parkinsonian syndromes

ID 221 – Disturbed eye movement control in Parkinson’s disease correlates with intrinsic functional connectivity within cortical networks

P18. Pattern of ‘resting-state’ functional hyperconnectivity in Amyotrophic lateral sclerosis reflects neuropathological disease stages

P19. The brain’s default mode is associated with executive oculomotor deficits in Parkinson’s disease

V13. Alterations of ‘resting-state’ functional connectivity in cognitively unimpaired and impaired patients with Parkinson’s disease

EPV 2. Spreading patterns of behavioral variant frontotemporal dementia: Analysis of longitudinal in vivo diffusion tensor imaging data

EP 50. Correlation between oculomotor changes and atlas-based volumetry in patients with different neurodegenerative Parkinson syndromes

FV 14. Longitudinal recordings of eye movements confirm the model of sequential oculomotor alterations in amyotrophic lateral sclerosis consistent with the neuropathological staging scheme

Stages of oculomotor dysfunctions confirms the model of axonal spread of pTDP-43 pathology in amyotrophic lateral sclerosis

ID 231 – Multicentric structural connectome analysis in 240 patients with amyotrophic lateral sclerosis

V42. De novo mutations in the FUS gene are a frequent cause of sporadic ALS in very young patients

Comparative phenotypical differences of Amyotrophic Lateral Sclerosis (ALS) in Germany and China

P 33. Investigation of microstructural alterations of ALS-specific tracts in asymptomatic ALS-mutation carriers

P-46 The effect of bevacizumab on cerebral microstructures in high-grade glioma

P-39 Hypothalamus volumetry in idiopathic intracranial hypertension: A controlled 3-D MRI study with BMI matching

Frontiers of amyotrophic lateral sclerosis cognitive assessment: The use of Eye-tracking and Brain Computer Interface in the eBrain project

Neurodevelopmental and neurodegenerative diseases – Is there a pathophysiological link? Attention-deficit/hyperactivity disorder and amyotrophic lateral sclerosis as examples

P 9 A multi-modal in vivo staging approach to amyotrophic lateral sclerosis

FV 3. Diagnostic value of oculomotor parameters in progressive supranuclear palsy: a monocentric study in 100 patients

Alcohol withdrawal syndrome: mechanisms, manifestations, and management

P-109 Association of disease severity and sequential alterations in diffusion metrics in amyotrophic lateral sclerosis

Erweiterte therapeutische Strategien bei neurologischen Erkrankungen: Gegenwart und Perspektiven

FV 5. MRI-based texture analysis of the corpus callosum in progressive supranuclear palsy

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