Dagmar Timmann

Dagmar Timmann

Department of Neurology and Center for Translational Neuro- and Behavioral Sciences (C-TNBS), Essen University Hospital

Affiliated withEssen University Hospital

Research Area

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JoVE Journal Publications

ArticleTotal : 1
Year
Neuronavigated Focalized Transcranial Direct Current Stimulation Administered During Functional Magnetic Resonance Imaging
Publication title

Cited by 14

2024

Other Publications

Article
Year
Age effects in storage and extinction of a naturally acquired conditioned eyeblink response.

Neurobiology of learning and memory| PubMed ID: 24365777

2014
Cerebellar cortex and cerebellar nuclei are concomitantly activated during eyeblink conditioning: a 7T fMRI study in humans.

The Journal of neuroscience : the official journal of the Society for Neuroscience| PubMed ID: 25609637

2015
2015
2015
2016
Cognition in Friedreich's ataxia: a behavioral and multimodal imaging study.

Annals of clinical and translational neurology| PubMed ID: 27606341

2016
2016
2017
2017
2017
2017
2018
2019
2018
2019
Standardized Assessment of Hereditary Ataxia Patients in Clinical Studies.

Movement disorders clinical practice| PubMed ID: 30363623

2016
2019
2019
2019
2019
Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar Ataxia.

Movement disorders : official journal of the Movement Disorder Society| PubMed ID: 31211461

2019
2019
Cerebellum is more concerned about visceral than somatic pain.

Journal of neurology, neurosurgery, and psychiatry| PubMed ID: 31558651

2020
2020
2019
2020
2020
2020
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C.

The Journal of clinical endocrinology and metabolism| PubMed ID: 33005949

2021
2020
2021
2020
2021
2021
Update cerebellum and cognition.

Journal of neurology| PubMed ID: 33656586

2021
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder.

Annals of clinical and translational neurology| PubMed ID: 33739604

2021
2021
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia.

Brain : a journal of neurology| PubMed ID: 33889951

2021
2021
2021
2021
2022
2022
2022
2022
2022
Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3.

Movement disorders : official journal of the Movement Disorder Society| PubMed ID: 35808813

2022
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.

Genetics in medicine : official journal of the American College of Medical Genetics| PubMed ID: 35986737

2022
Bi-Allelic COQ4 Variants Cause Adult-Onset Ataxia-Spasticity Spectrum Disease.

Movement disorders : official journal of the Movement Disorder Society| PubMed ID: 36047608

2022
2022
Progressive Spinal Cord Degeneration in Friedreich's Ataxia: Results from ENIGMA-Ataxia.

Movement disorders : official journal of the Movement Disorder Society| PubMed ID: 36308733

2023
2023
2023
Autosomal Recessive Cerebellar Ataxias in Europe: Frequency, Onset, and Severity in 677 Patients.

Movement disorders : official journal of the Movement Disorder Society| PubMed ID: 37027459

2023
The cerebellum and fear extinction: evidence from rodent and human studies.

Frontiers in systems neuroscience| PubMed ID: 37152612

2023
2024
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.

American journal of human genetics| PubMed ID: 37301203

2023
2024
2023
2023
2024
Neurophysiology of cerebellar ataxias and gait disorders.

Clinical neurophysiology practice| PubMed ID: 37593693

2023
2023
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.

Genetics in medicine : official journal of the American College of Medical Genetics| PubMed ID: 37650884

2023
2024
2024
2024
2024
2024
Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study.

Journal of neurology, neurosurgery, and psychiatry| PubMed ID: 38383154

2024
2024
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): from clinical diagnosis towards genetic testing.

Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V| PubMed ID: 38835435

2021
2024
2024
2024
2024
2024
2024