Results 211 to 220 of about 546,155 (300)

Lance-Adams syndrome following suicidal hanging: A rare complication initially misdiagnosed as dissociative motor disorder. [PDF]

Indian J Psychiatry
Aggarwal A, Garg S.
europepmc   +1 more source

Should Paratonia Be Considered a Movement Disorder? Implications for Clinical Management

Movement Disorders Clinical Practice, EarlyView.
Abstract Paratonia is an involuntary and variable resistance to passive movement that emerges with cognitive decline in dementias of different etiologies, with prevalence approaching 90% to 100% in end‐stage disease. It is common in Parkinson disease and the atypical parkinsonisms.
Galit Kleiner, Christos Ganos, Anthony E. Lang   +2 more
wiley   +1 more source

Diagnostic Dilemma in an Infant With Sound-Triggered Motor Events: Reflex Epilepsy Versus Exaggerated Startle-A Case Report. [PDF]

Clin Case Rep
Pandit A, Koirala M, Shahi A, Sharma A, Panta A, Rimal S.   +5 more
europepmc   +1 more source

From Uncertainty to Pathogenicity: Resolving a CSF1R Variant of Uncertain Significance Using Long‐Read Transcriptomics

Movement Disorders, EarlyView.
Abstract Background CSF1R‐related disorder (CSF1R‐RD) is a severe autosomal dominant leukoencephalopathy characterized by progressive cognitive, neuropsychiatric, and motor decline. Although genetic testing is widely available, numerous likely pathogenic variants in CSF1R frequently remain classified as variants of uncertain significance (VUS ...
Charles Wade, Kylie Montgomery, Gabriela E. Jones, Peter Sellars, Akram A. Hosseini, Simon Paine, Henry Houlden, Mina Ryten, David S. Lynch   +8 more
wiley   +1 more source

Recent advances in clinical neurophysiology of myoclonus. [PDF]

Clin Park Relat Disord
Grippe T, Angeloni B, Bhattacharya A, Chen R.   +3 more
europepmc   +1 more source

Early Longitudinal Brain Network Changes in Huntington's Disease Before Clinical Motor Onset

Movement Disorders, EarlyView.
Abstract Background Longitudinal studies of seed‐based functional connectivity (SBFC) in young adult Huntington's disease gene‐expanded (HDGE) individuals are rare, and none, to our knowledge, have examined adult cohorts decades from predicted clinical motor diagnosis.
Michela Leocadi, Nicola Z. Hobbs, Mena Farag, Michael J. Murphy, Kate Fayer, Olivia Thackeray, Harry Knights, James B. Rowe, Trevor W. Robbins, Barbara J. Sahakian, Geraint Rees, Rachael I. Scahill, Sarah J. Tabrizi, Christelle Langley   +13 more
wiley   +1 more source

Long-term neuromuscular alterations during botulinum toxin treatment for chronic migraine. [PDF]

Clin Neurophysiol Pract
Plensäll T, Liik M, Pogosean A, Eriksson A, Garrett M, Olszowy J, Jackmann S, Punga AR.   +7 more
europepmc   +1 more source

Reconsidering the Pathophysiological Interpretation of Polyphasic LSRs in Hemifacial Spasm. [PDF]

Neurol Med Chir (Tokyo)
Choi J.
europepmc   +1 more source

Beyond Analytical Agreement: Integrating Analytical Performance and Algorithm-Assisted Morphological Interpretation in a Comparative Evaluation of the Mindray BC-7800/BC-7900 and Sysmex XN-9100 Hematology Platforms. [PDF]

Diagnostics (Basel)
Ciullini Mannurita S, Romeo D, Bonari A, Russo E, Nardiello P, Becherucci V, Vitali D, Fanelli A, Romano F.   +8 more
europepmc   +1 more source