Author

Herwig W. Lange

Observed names: H. W. Lange, H.-W. Lange, H.W Lange, H.W. LANGE, H.W. Lange, HERWIG W. LANGE, Herwig Lange, Herwig W Lange, Lange, Herwig, Lange, Herwig W.

Institutions: Düsseldorf University Hospital, Heinrich Heine University Düsseldorf

Observed institutions: Forschungszentrum Jülich, University of Münster, TUM Klinikum, Medizinische Hochschule Hannover, Düsseldorf University Hospital, University Hospital Münster, Max Planck Institute of Psychiatry, Gloucestershire Royal Hospital, Alfried Krupp Hospital, Reha Rheinfelden, George Huntington Institute, Heinrich Heine University Düsseldorf, Technical University of Munich, Cardiff University

ORCID: 0000-0003-0718-4001

Observed ORCID: 0000-0003-0718-4001

OpenAlex ID: A5111920604

Loss of disgust

1996 · Reiner Sprengelmeyer, Andrew W. Young, et al. · Brain · 459

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

2012 · J.-M. Lee, E.M. Ramos, et al. · Neurology · 382

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

2017 · Davina J Hensman Moss, Antonio F Pardiñas, et al. · The Lancet Neurology · 310

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Cortical and Subcortical Glucose Consumption Measured by Pet in Patients With Huntington's Disease

1990 · TORSTEN KUWERT, HERWIG W. LANGE, et al. · Brain · 279

Impairment of Rapid Movement in Huntington's Disease

1987 · HARALD HEFTER, VOLKER HÖMBERG, et al. · Brain · 145

Velocity modulation and rhythmic synchronization of gait in Huntington's disease

1999 · Michael H. Thaut, Rgina Miltner, et al. · Movement Disorders · 125

Language Functions in Huntington's Disease

1988 · KLAUS PODOLL, PETER CASPARY, et al. · Brain · 116

Recognition of Facial Expressions: Selective Impairment of Specific Emotions in Huntington's Disease

1997 · Reiner Sprengelmeyer, Andrew W. Young, et al. · Cognitive Neuropsychology · 106

Striatal glucose consumption in chorea-free subjects at risk of Huntington's disease

1993 · T. Kuwert, H. Boecker, et al. · Journal of Neurology · 99

Evoked potentials in patients with Huntington's disease and their offspring. I. Somatosensory evoked potentials

1984 · J Noth, L Engel, et al. · Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section · 84

Associative learning in degenerative neostriatal disorders: Contrasts in explicit and implicit remembering between Parkinson's and huntington's diseases

1995 · R. Sprengelmeyer, A. G. M. Canavan, et al. · Movement Disorders · 71

H untington's D isease ( HD ): Degeneration of Select Nuclei, Widespread Occurrence of Neuronal Nuclear and Axonal Inclusions in the Brainstem

2013 · Udo Rüb, Matthias Hentschel, et al. · Brain Pathology · 63

Motor learning by imagery is differentially affected in Parkinson’s and Huntington’s diseases

1999 · Lidia Yágüez, Anthony G.M Canavan, et al. · Behavioural Brain Research · 62

Assessment of involuntary choreatic movements in Huntington's disease—Toward objective and quantitative measures

2011 · Ralf Reilmann, Stefan Bohlen, et al. · Movement Disorders · 59

Impairment of retinal increment thresholds in Huntington's disease

1993 · Walter Paulus, Guntram Schwarz, et al. · Annals of Neurology · 56

Clinical manifestations of intermediate allele carriers in Huntington disease

2016 · Esther Cubo, María A. Ramos-Arroyo, et al. · Neurology · 53

Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's disease

2010 · Ralf Reilmann, Stefan Bohlen, et al. · Movement Disorders · 49

What is the impact of education on Huntington's disease?

2011 · Jose Luis López‐Sendón, Ana Royuela, et al. · Movement Disorders · 47

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease

2005 · Silke Metzger, Peter Bauer, et al. · Neurogenetics · 47

Grasping premanifest Huntington's disease – shaping new endpoints for new trials

2010 · Ralf Reilmann, Stefan Bohlen, et al. · Movement Disorders · 45

The diagnostic value of eye movement recording in patients with Huntington's disease and their offspring

1986 · N. Beenen, U. Büttner, et al. · Electroencephalography and Clinical Neurophysiology · 45

Comparison of somatosensory evoked potentials with striatal glucose consumption measured by positron emission tomography in the early diagnosis of huntington's disease

1993 · T. Kuwert, J. Noth, et al. · Movement Disorders · 44

Absence of long latency reflexes to imposed finger displacements in patients with Huntington's disease

1983 · J. Noth, H.-H. Friedemann, et al. · Neuroscience Letters · 44

Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease

2006 · Silke Metzger, Peter Bauer, et al. · Human Genetics · 42

Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study

2018 · Paul McNulty, Richard Pilcher, et al. · Journal of Huntington s Disease · 35

Works count: 59

Citation count: 3,579

H-index: 30

I10-index: 43