Results 151 to 160 of about 59,798 (297)
Movement Disorders Clinical Practice, EarlyView.ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan +4 more
wiley +1 more source
Opsoclonus myoclonus syndrome: how long are we going to go on researching?] [PDF]
, 2002 Rev Neurol. 2002 Aug 16-31;35(4):322-5. [Opsoclonus myoclonus syndrome: how long are we going to go on researching?] [Article in Spanish] Ramos S, Temudo T. Interna complementar de Pediatria. Serviço de Pediatria.
Ramos, S., Temudo, T.
core
Fragmentary myoclonus in idiopathic rapid eye movement sleep behaviour disorder [PDF]
, 2019 Jiří Nepožitek +14 more
openalex +1 more source
Palatal myoclonus and hypertrophic olivary degeneration following Wernekinck Commissure Syndrome: a case report [PDF]
, 2022 Qian Zhang +4 more
openalex +1 more source
A Case of Multiple Sclerosis Presenting as Eight and Half Syndrome. [PDF]
, 2013 Multiple sclerosis (MS) is a chronic disease characterized by inflammation, demyelination, gliosis (scarring), and neuronal loss; the course can be relapsing-remitting or progressive.
Kaushik, M +4 more
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Convergence Deficits in Myoclonus‐Dystonia Point to Cerebellar Impairment
Movement Disorders Clinical Practice, EarlyView.Abstract Background Myoclonus‐dystonia (M‐D) is a monogenic movement disorder, with proposed cerebellar dysfunction. Vergence eye movement deficits, characteristics of degenerative cerebellar disease, have not been studied in M‐D. Cerebellar transcranial alternating current stimulation (tACS) is considered a potential therapeutic approach.
Skadi Gerkensmeier +13 more
wiley +1 more source
Integrating Long‐Read Nanopore Sequencing for Precision Resolution of Genomic Variants in Dystonia
Movement Disorders, EarlyView.Abstract Background Although many individuals with dystonia present with features indicative of single‐gene etiologies, obtaining definitive genetic diagnoses can be challenging. Objective We assessed the value of nanopore‐based long‐read sequencing (LRS) in achieving molecular clarification of dystonic syndromes.
Ugo Sorrentino +30 more
wiley +1 more source
Interdisciplinary NeurosurgeryObjects: Lance Adams syndrome (LAS) is a chronic post-hypoxic myoclonus that predominantly arises following successful cardiopulmonary resuscitation; however, there are so rare instances following respiratory failure.
Amir Reza Bahadori +8 more
doaj +1 more source
Rare but Relevant? Assessing Variants in Dystonia‐Linked Genes in Parkinson's Disease
Movement Disorders, EarlyView.Abstract Background Dystonia and Parkinson's disease (PD) exhibit clinical and genetic overlap, but the relevance of dystonia gene variants in PD remains unclear. Objective The aim was to assess the frequency of dystonia‐linked pathogenic variants in PD.
Lara M. Lange +37 more
wiley +1 more source