Schöls, Ludger

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients

Schüle, R., Wiethoff, S., Martus, P., Karle, K. N., Otto, S., Klebe, S., Klimpe, S., Gallenmüller, C., Kurzwelly, D., Henkel, D., et al. (2016) · Annals of Neurology

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 315

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

Montenegro, G., Rebelo, A. P., Connell, J., Allison, R., Babalini, C., D’Aloia, M., Montieri, P., Schüle, R., Ishiura, H., Price, J., et al. (2012) · Journal of Clinical Investigation

Hereditary Neurological DisordersGenetic Neurodegenerative Diseases

Cited by 170

Loss of nocturnal blood pressure fall in various extrapyramidal syndromes

Schmidt, C., Berg, D., Herting, Prieur, S., Junghanns, S., Schweitzer, K., Globas, C., Schöls, L., Reichmann, H., & Ziemssen, T. (2009) · Movement Disorders

Parkinson's Disease Mechanisms and TreatmentsCardiovascular Syncope and Autonomic Disorders

Cited by 113

Defining diagnostic cutoffs in neurological patients for serum very long chain fatty acids (VLCFA) in genetically confirmed X-Adrenoleukodystrophy

Rattay, T. W., Rautenberg, M., Söhn, A. S., Hengel, H., Traschütz, A., Röben, B., Hayer, S. N., Schüle, R., Wiethoff, S., Zeltner, L., et al. (2020) · Scientific Reports

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 61

Tau and neurofilament light‐chain as fluid biomarkers in spinocerebellar ataxia type 3

Garcia‐Moreno, H., Prudencio, M., Thomas‐Black, G., Solanky, N., Jansen‐West, K. R., Hanna AL‐Shaikh, R., Heslegrave, A., Zetterberg, H., Santana, M. M., Pereira de Almeida, L., et al. (2022) · European Journal of Neurology

Genetic Neurodegenerative DiseasesAmyotrophic Lateral Sclerosis Research

Cited by 49

ADHD candidate gene (DRD4 exon III) affects inhibitory control in a healthy sample

Krämer, U. M., Rojo, N., Schüle, R., Cunillera, T., Schöls, L., Marco-Pallarés, J., Cucurell, D., Camara, E., Rodriguez-Fornells, A., & Münte, T. F. (2009) · BMC Neuroscience

Attention Deficit Hyperactivity DisorderNeurotransmitter Receptor Influence on Behavior

Cited by 42

Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophic

Rattay, T. W., Just, J., Röben, B., Hengel, H., Schüle, R., Synofzik, M., Söhn, A. S., Winter, N., Dammeier, N., Schöls, L., et al. (2018) · Orphanet Journal of Rare Diseases

Hereditary Neurological DisordersPeripheral Nerve Disorders

Cited by 14

Leriglitazone: Frustration and hope in adrenoleukodystrophy

Schöls, L. (2023) · The Lancet Neurology

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 4