Results 241 to 250 of about 61,761 (310)
Progranulin Mutation Manifesting as Parkinson Disease: A Case Series from the PADUA‐CESNE Cohort
Movement Disorders Clinical Practice, EarlyView.Abstract Background Mutations in progranulin (GRN) are associated with frontotemporal dementia, although a Parkinson disease (PD) phenotype is uncommon, especially in young patients. Cases We report three subjects from the PADUA‐CESNE cohort, meeting diagnostic criteria for PD, with onset under age 55.
Giulia Bonato +8 more
wiley +1 more source
How do I Know That the Jerks I See Are Tics?
Movement Disorders Clinical Practice, EarlyView.Tics are prevalent hyperkinesias that are most often encountered in the context of a primary tic disorder, as in Tourette syndrome. Although their recognition is typically straightforward, they often share some phenomenological features with other jerky hyperkinesias and may be mislabeled as such.
Talyta Grippe +2 more
wiley +1 more source
[Normal Anatomy of Cranial Nerves III-XII on Magnetic Resonance Imaging]. [PDF]
Taehan Yongsang Uihakhoe Chi, 2020 Kim HJ, Seong M, Kim Y.
europepmc +1 more source
Myoclonic Dystonia: A Common Phenomenology in the Pleomorphic Movements of Angelman Syndrome
Movement Disorders Clinical Practice, EarlyView.Abstract Background Angelman syndrome (AS) is a neurodevelopmental disorder characterized by developmental delay, intellectual disability, a sociable demeanor, and abnormal movements. People with AS often exhibit multiple types of abnormal movements, including nonepileptic myoclonus, tremor, and dystonia, which hamper attempts to identify phenomenology
Robert P. Carson +8 more
wiley +1 more source
The emerging role of cranial nerves in shaping craniofacial development. [PDF]
Genesis, 2019 Sudiwala S, Knox SM.
europepmc +1 more source
Enterovirus A‐71 Associated Parainfectious Movement Disorders in Children
Movement Disorders Clinical Practice, EarlyView.Abstract Background Pediatric movement disorders can be challenging to characterize, given the phenotypic complexity and broad differential diagnosis. While genetic tests are often part of the diagnostic work‐up, it is important to consider acquired causes, which may require specific investigations.
Suus A. M. van Noort +6 more
wiley +1 more source