Results 161 to 170 of about 59,407 (333)

ADCY5‐Mosaic Variants: A Diagnosis Not to Be Missed

Movement Disorders Clinical Practice, EarlyView.
Abstract Background An increasing number of ADCY5‐mosaic patients, seemingly with a milder phenotype, are being identified. However, an in‐depth assessment of their clinical characteristics is lacking. Cases We collected and analyzed data from 12 consecutive ADCY5‐mosaic patients diagnosed at our center and 7 cases from the literature; 63% of the ...
Alice Innocenti, Emmanuel Roze, Florence Riant, Marie‐Céline François‐Heude, Bérénice Lecardonnel, Giacomo Garone, Maxime Colmard, Eline Chauvet‐Piat, Anne‐Cécile Chaux, Marie‐Aude Spitz, Beatrice Desnous, Catherine Sarret, Philippe Damier, Thomas Wirth, Mathieu Anheim, Emilie Retailleau, Estelle Conabady, Caroline Dubacq, Oriane Trouillard, Aurélie Méneret, Agathe Roubertie   +20 more
wiley   +1 more source

Memory guided saccade deficit after caudate nucleus lesion [PDF]

, 1999
A. I. Vermersch, Bertrand Gaymard, Sophie Rivaud-Péchoux, Christoph J. Ploner, Y. Agid, C. Pierrot‐Deseilligny   +5 more
openalex   +1 more source

Long‐Term Benefit of Thalamic Deep Brain Stimulation in POLR3A Mutation‐Associated Action Tremor

Movement Disorders Clinical Practice, EarlyView.
Martina Minnerop, Alisha Reinhardt, Petyo Nikolov, Bahne H. Bahners, Julian Caspers, Julia Gelenar Marae, Christian J. Hartmann, Stefan J. Groiss, Katrin Amunts, Jan Vesper, Alfons Schnitzler   +10 more
wiley   +1 more source

saccades

https://aimc2024.pubpub.org/pub/vftqi55v/release ...
openaire   +2 more sources

Saccadic suppression [PDF]

Current Biology, 2010
openaire   +2 more sources

Repeat Expansions with Small TTTCA Insertions in MARCHF6 Cause Familial Myoclonus without Epilepsy

Movement Disorders, EarlyView.
Abstract Background Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder caused by the same intronic TTTTA/TTTCA repeat expansion in seven distinct genes. TTTTA‐only expansions are benign, whereas those containing TTTCA insertions are pathogenic.
Theresa Kühnel, Elsa Leitão, Renate Lunzer, Fabian Kilpert, Sabine Kaya, Claudia Del Gamba, Kelly Astudillo, Steven Frucht, Marion Simonetta‐Moreau, Eric Bieth, Iris Unterberger, Giulietta Maria Riboldi, Christel Depienne   +12 more
wiley   +1 more source

Application and progress of advanced eye movement examinations in cognitive impairment

Frontiers in Aging Neuroscience
The worldwide incidence of cognitive impairment is escalating, yet no effective solutions for these afflictions have been discovered. Consequently, the importance of early identification and immediate intervention is heightened.
Qi Leng, Bo Deng, Yi Ju, Yi Ju
doaj   +1 more source

Blinks, Saccades, and Fixation Pauses During Vigilance Task Performance: II. Gender and Time of Day [PDF]

, 1996
John A. Stern, David J. Schroeder, Robert M. Touchstone, Nikolai Stoliarov, Donna Boyer   +4 more
openalex   +1 more source

Not So Smooth Sailing: FIG4‐Related Disease Is a Differential Diagnosis of Rapid Onset Dystonia‐Parkinsonism

Movement Disorders Clinical Practice, EarlyView.
Matthew Julian Georgiades, Duncan Wilson, Maria Garcia, Robert Boland‐Freitas, Hugo Morales‐Briceño, Neil Mahant, Victor Shue Chung Fung, Andrew Martin   +7 more
wiley   +1 more source

Nocebo Hypothesis Cognitive Behavioral Therapy for Functional Neurological Symptom Disorder (Motor Type): A Pilot Randomized Controlled Trial

Movement Disorders, EarlyView.
Abstract Background A previous case series showed that Nocebo Hypothesis Cognitive Behavioral Therapy (NH‐CBT) is a promising treatment for Functional Neurological Symptom Disorder (FNSD). Objectives To further evaluate the potential efficacy of NH‐CBT in participants with FNSD (motor type).
Matt Richardson, Maria Kleinstäuber, Dana Wong   +2 more
wiley   +1 more source