Results 131 to 140 of about 42,432 (196)

Postural balance disorders in sarcopenia based on surface electromyography. [PDF]

Heliyon
Zhang T, Huo Y, Yin W, Xiang J.
europepmc   +1 more source

Parkinsonism and Dystonia Are Prevalent and Concomitant Movement Disorders in a Cohort of Patients with Rett Syndrome

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Rett syndrome (RTT) is a rare neurodevelopmental disorder linked with MECP2 variants, frequently presenting with movement disorders (MDs). Objectives This study examined the frequency, types, and associations of MDs with RTT characteristics and severity.
Silvia Boeri, Giulia Prato, Maria Grazia Calevo, Silvia Casabona, Lino Nobili, Elisa De Grandis   +5 more
wiley   +1 more source

Child and Adolescent Manganese Biomarkers and Adolescent Postural Balance in Marietta CARES Cohort Participants. [PDF]

Environ Health Perspect
McBride DE, Bhattacharya A, Sucharew H, Brunst KJ, Barnas M, Cox C, Altman L, Hilbert TJ, Burkle J, Westneat S, Martin KV, Parsons PJ, Praamsma ML, Palmer CD, Kannan K, Smith DR, Wright R, Amarasiriwardena C, Dietrich KN, Cecil KM, Haynes EN.   +20 more
europepmc   +1 more source

Breaking Boundaries: Chronic Diseases and the Frontiers of Immune Microenvironments

Med Research, EarlyView.
ABSTRACT The immune microenvironment includes immune cells, cytokines, extracellular matrix, vesicles, etc. The interactions between these components form a unique local immune microecology. Although immunity serves as the defense against external pathogens, aberrant immune activation often contributes to disease development.
Guoqing Li, Yuxuan Wan, Alan Jiao, Ke Jiang, Gaoyuan Cui, Jinxin Tang, Simin Yu, Zhengang Hu, Songfeng Zhao, Zhenjie Yi, Lifu Long, Yang Yang, Xuehao Cui, Chunrun Qu   +13 more
wiley   +1 more source

Long‐Term Outcomes on Pallidal Neurostimulation for Dystonia: A Controlled, Prospective 10‐Year Follow‐Up

Movement Disorders, EarlyView.
Abstract Background Pallidal neurostimulation is an effective treatment for severe isolated dystonia, but long‐term data from clinical trials are lacking. Objectives To evaluate long‐term efficacy and safety of pallidal neurostimulation in patients with isolated generalized or segmental dystonia.
Patricia Krause, Philipp Mahlknecht, Inger Marie Skogseid, Frank Steigerwald, Günther Deuschl, Richard Erasmi, Alfons Schnitzler, Tobias Warnecke, Jörg Müller, Werner Poewe, Gerd‐Helge Schneider, Jan Vesper, Nils Warneke, Wilhelm Eisner, Thomas Prokop, Jan‐Uwe Müller, Jens Volkmann, Andrea A. Kühn, for the Deep‐Brain Stimulation for Dystonia Study Group, Maximilian Mehdorn, Patricia Krause, Doreen Gruber, Anatol Kivi, Andreas Kupsch, Bianca Müller, Gerd‐Helge Schneider, Alfons Schnitzler, Volker Sturm, Lars Timmermann, Jürgen Voges, Lars Wojtecki, Guido Nikkah, Markus Pinsker, Thomas Prokop, Jan Vesper, Manja Kloss, Martin Krause, Volker Tronnier, Wilhelm Eisner, Thomas Fiegele, Jörg Müller, Sasha Hering, Werner Poewe, Günther Deuschl, Jan Herzog, Marcus O Pinsker, Monika Pötter‐Nerger, Frank Steigerwald, Hans‐Werner Boothe, Angela Brentrup, Juliane Vollmer‐Haase, Inger Marie Skogseid, Geir Ketil Roeste, Jan‐Uwe Müller, Matthias Wittstock, Alexander Wolters, Joseph Classen, Markus Naumann, Alex Schramm, Jens Volkmann, Andrea A. Kühn   +60 more
wiley   +1 more source

Postural balance in COPD with obstructive sleep apnoea: a cross-sectional study. [PDF]

ERJ Open Res
de Censo CM, Passini VV, Verri BATA, Xavier RF, Carvalho-Pinto RM, Lorenzi-Filho G, Carvalho CRF.   +6 more
europepmc   +1 more source

Novel In‐Frame FGF14 Deletion Causes Spinocerebellar Ataxia Type 27A: Clinical Response to Deep Brain Stimulation and 4‐Aminopyridine

Movement Disorders, EarlyView.
Abstract Background Spinocerebellar ataxia 27A (SCA27A) is a rare neurodegenerative disorder characterized by childhood‐onset tremor and progressive cerebellar dysfunction. SCA27A is usually caused by loss‐of‐function FGF14 variants. Objectives We report the identification of a novel FGF14 variant in a five‐generation family with autosomal dominant ...
Ignacio J. Keller Sarmiento, Roberta Bovenzi, Morgan Kinsinger, Lisa Kinsley, Bernabe I. Bustos, Dimitri Krainc, Niccolò E. Mencacci   +6 more
wiley   +1 more source

Cholinergic System Changes in Dopa‐Unresponsive Freezing of Gait in Parkinson's Disease

Movement Disorders, EarlyView.
Abstract Background Freezing of gait (FoG) is a debilitating mobility disturbance that becomes increasingly resistant to dopaminergic pharmacotherapies with advancing Parkinson's disease (PD). The pathophysiology underlying the response of FoG to dopaminergic treatment is poorly understood.
Kelvin L. Chou, Prabesh Kanel, Miriam van Emde Boas, Stiven Roytman, Giulia Carli, Roger L. Albin, Nicolaas I. Bohnen   +6 more
wiley   +1 more source

Paired Deep Brain Stimuli Elicit Short‐Term Facilitation in Globus Pallidus Interna and Subthalamic Nucleus

Movement Disorders, EarlyView.
Abstract Background Deep brain stimulation (DBS) elicits oscillatory local field potentials in patients with Parkinson's disease (PD) and other movement disorders. Greater knowledge about the fast dynamics of these neural responses could shed light on circuit pathophysiology and inform novel approaches to neuromodulation therapies.
Sarah Brinkerhoff, Arie Nakhmani, Alex Varghese, Cameron Gordon, Christopher L. Gonzalez, J. Nicole Bentley, Marshall T. Holland, Harrison C. Walker   +7 more
wiley   +1 more source

Compressive Cervical Myelopathy Causing Impaired Gait after Deep Brain Stimulation Is Not Rare

Movement Disorders Clinical Practice, EarlyView.
Caroline Weill, Sami Heymann, Roy Dayan, Eduard Linetsky, Hagai Bergman, Zvi Israel, David Arkadir   +6 more
wiley   +1 more source