Results 71 to 80 of about 1,376 (192)
Brazilian Journal of Otorhinolaryngology, 2011 Dystonia is a central motor processing neurological disorder characterized by abnormal, often action-induced, involuntary movements or uncontrolled spasms.
Gustavo Polacow Korn +6 more
doaj +1 more source
Kandidatengenstudien bei Fokaler Idiopathischer Torsionsdystonie (F-ITD) [PDF]
, 2005 Bei der fokalen idiopathischen Torsionsdystonie (F-ITD) handelt es sich um die häufigste Form der Dystonien, wobei die Ätiologie dieser Erkrankung bisher nicht geklärt ist.
Bandmann, Oliver (PD Dr. med.) +1 more
core +1 more source
Severity‐Based and Family‐Centered Approaches to Deep Brain Stimulation in GNAO1‐Related Disorders
Movement Disorders Clinical Practice, EarlyView.
Jana Domínguez‐Carral +1 more
wiley +1 more source
Movement Disorders, Volume 41, Issue 4, Page 856-869, April 2026.Abstract Background Membrane contact sites are crucial for the exchange of ions or lipids and thus are critical for the function and maintenance of organelles. VPS13A is a membrane‐residing, bridge‐like protein connecting two membranes to enable bulk lipid transfer. Loss‐of‐function mutations in the VPS13A gene cause VPS13A disease.
Dajana Grossmann +10 more
wiley +1 more source
Asymmetric Upper Limb Dysfunction Demonstrated at the Bedside: A Phenomenology Video
Movement Disorders Clinical Practice, EarlyView.
Gero Lueg +4 more
wiley +1 more source
International Registry of NKX2‐1‐Related Disorders: Clinical, Genetic, and Imaging Perspectives
Movement Disorders, Volume 41, Issue 4, Page 889-900, April 2026.Abstract Background NKX2‐1–related disorders result from heterozygous variants in NKX2‐1, a gene crucial for brain, lung, and thyroid development. Although movement disorders, hypothyroidism, and neonatal respiratory distress are recognized, the full phenotype and genotype–phenotype relationships remain incompletely defined.
Laia Nou‐Fontanet +47 more
wiley +1 more source
A Short Commentary on Globus Pallidus Internus Deep Brain Stimulation in Primary Meige Syndrome [PDF]
, 2016 Meige syndrome is a type of segmental dystonia that manifests a combination of blepharospasm and oromandibular dystonia and is often associated with other types of craniocervical dystonia.
261538/profile-ja.html +10 more
core
Movement Disorders in Neuromyelitis Optica Spectrum Disorder: A Systematic Review
Movement Disorders Clinical Practice, Volume 13, Issue 3, Page 600-610, March 2026.Abstract Background Several movement disorders (MD) have been reported to occur in neuromyelitis optica spectrum disorder (NMOSD). No extensive review has addressed the whole spectrum of MD in NMOSD. Objective This article aims to review MD in NMOSD, describing its prevalence and features.
Luciana A.F. Bringel +18 more
wiley +1 more source
Historical aspects of studying craniocervical dystonia
Анналы клинической и экспериментальной неврологии, 2019 The study of dystonic hyperkinesias has a thousand-year-old history. Beginning with drawings and sculptures from antiquity and up to the present day, modern ideas gradually developed about the phenomenology, origin, and treatment methods of dystonia ...
Zifa G. Khayatova, Zuleykha A. Zalyalova
doaj +1 more source
Movement Disorders Clinical Practice, Volume 13, Issue 3, Page 774-778, March 2026.Abstract Background Anticholinergic medications and botulinum neurotoxin injections are established treatments for dystonia, yet they carry potential side effects and practical challenges. Deep brain stimulation (DBS) is offered in case of poor response to these approaches.
Marcela A. Montiel +5 more
wiley +1 more source