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Petr Dusek

Showing results (51-60 of 79) with videos related to

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Molecular Genetics and Metabolism|December 15, 2020
White matter alteration and cerebellar atrophy are hallmarks of brain MRI in alpha-mannosidosisJitka Majovska, Igor Nestrasil, Amy Paulson, et al.
Biomedicines|February 25, 2023
A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and TreatmentLouis C Penning, Marina Berenguer, Anna Czlonkowska, et al.
International Journal of Molecular Sciences|June 28, 2023
CSF Markers of Oxidative Stress Are Associated with Brain Atrophy and Iron Accumulation in a 2-Year Longitudinal Cohort of Early MSAndrea Burgetova, Petr Dusek, Tomas Uher, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|June 6, 2025
Colour discrimination deficit in REM sleep behavior disorder: an analysis of dopaminergic depletion, cognition, and brain morphologyFilip Havlik, Christiane Mala, Petr Dusek, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|August 5, 2016
MRI phase changes in multiple sclerosis vs neuromyelitis optica lesions at 7TTim Sinnecker, Sophie Schumacher, Katharina Mueller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 17, 2024
Is speech function lateralised in the basal ganglia? Evidence from de novo Parkinson's diseaseJan Rusz, Petr Dusek, Tereza Tykalova, et al.
European Journal of Radiology|October 15, 2015
Ultrahigh-field MPRAGE Magnetic Resonance Angiography at 7.0 T in patients with cerebrovascular diseaseVince I Madai, Federico C von Samson-Himmelstjerna, Nora Sandow, et al.
Magma (New York, N.Y.)|April 14, 2016
Neuromyelitis optica does not impact periventricular venous density versus healthy controls: a 7.0 Tesla MRI clinical studySophie Schumacher, Florence Pache, Judith Bellmann-Strobl, et al.
American Journal of Medical Genetics. Part A|November 16, 2019
Alu-mediated Xq24 deletion encompassing CUL4B, LAMP2, ATP1B4, TMEM255A, and ZBTB33 genes causes Danon disease in a female patientFilip Majer, Bohdan Kousal, Petr Dusek, et al.
Journal of Sleep Research|January 25, 2019
Fragmentary myoclonus in idiopathic rapid eye movement sleep behaviour disorderJiri Nepozitek, Simona Dostalova, David Kemlink, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Molecular Genetics and Metabolism|December 15, 2020
White matter alteration and cerebellar atrophy are hallmarks of brain MRI in alpha-mannosidosisJitka Majovska, Igor Nestrasil, Amy Paulson, et al.
Biomedicines|February 25, 2023
A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and TreatmentLouis C Penning, Marina Berenguer, Anna Czlonkowska, et al.
International Journal of Molecular Sciences|June 28, 2023
CSF Markers of Oxidative Stress Are Associated with Brain Atrophy and Iron Accumulation in a 2-Year Longitudinal Cohort of Early MSAndrea Burgetova, Petr Dusek, Tomas Uher, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|June 6, 2025
Colour discrimination deficit in REM sleep behavior disorder: an analysis of dopaminergic depletion, cognition, and brain morphologyFilip Havlik, Christiane Mala, Petr Dusek, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|August 5, 2016
MRI phase changes in multiple sclerosis vs neuromyelitis optica lesions at 7TTim Sinnecker, Sophie Schumacher, Katharina Mueller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 17, 2024
Is speech function lateralised in the basal ganglia? Evidence from de novo Parkinson's diseaseJan Rusz, Petr Dusek, Tereza Tykalova, et al.
European Journal of Radiology|October 15, 2015
Ultrahigh-field MPRAGE Magnetic Resonance Angiography at 7.0 T in patients with cerebrovascular diseaseVince I Madai, Federico C von Samson-Himmelstjerna, Nora Sandow, et al.
Magma (New York, N.Y.)|April 14, 2016
Neuromyelitis optica does not impact periventricular venous density versus healthy controls: a 7.0 Tesla MRI clinical studySophie Schumacher, Florence Pache, Judith Bellmann-Strobl, et al.
American Journal of Medical Genetics. Part A|November 16, 2019
Alu-mediated Xq24 deletion encompassing CUL4B, LAMP2, ATP1B4, TMEM255A, and ZBTB33 genes causes Danon disease in a female patientFilip Majer, Bohdan Kousal, Petr Dusek, et al.
Journal of Sleep Research|January 25, 2019
Fragmentary myoclonus in idiopathic rapid eye movement sleep behaviour disorderJiri Nepozitek, Simona Dostalova, David Kemlink, et al.
Pageof 8