Results 301 to 310 of about 234,277 (395)

Homozygous DNAJC6 Mutated Juvenile Onset Dystonia‐Parkinsonism Is Responsive to Pallidal Deep Brain Stimulation

Movement Disorders Clinical Practice, Volume 12, Issue 3, Page 392-396, March 2025.
James Manfield, Marko Bogdanovic, Nagaraja Sarangmat, Sangeeta Scotton, Alexander L. Green, James Fitzgerald   +5 more
wiley   +1 more source

Effects of intermittent theta burst stimulation versus repetitive transcranial magnetic stimulation on post-stroke dysphagia in hospitalised patients: study protocol for a prospective, randomised controlled trial. [PDF]

BMJ Open
Chen X, Zhu J, Bai W, Li X, Yang M, Wang J, Yu J, Jian R.   +7 more
europepmc   +1 more source

A quantitative study of videofluorography using a personal computer. Analysis of postoperative dysphagia of oral and oropharyngeal cancer patients.

, 1996
Yasushi Fujimoto, Yasuhisa Hasegawa, Hidehiro Matsuura, Bin Nakayama   +3 more
openalex   +2 more sources

Gut Microbial Metabolites and Future Risk of Parkinson's Disease: A Metabolome‐Wide Association Study

Movement Disorders, Volume 40, Issue 3, Page 556-560, March 2025.
Abstract Background Alterations in gut microbiota are observed in Parkinson's disease (PD). Previous studies on microbiota‐derived metabolites in PD were small‐scale and post‐diagnosis, raising concerns about reverse causality. Objectives Our goal was to prospectively investigate the association between plasma microbial metabolites and PD risk within a
Yujia Zhao, Yunjia Lai, Sirwan K.L. Darweesh, Bastiaan R. Bloem, Lars Forsgren, Johnni Hansen, Verena A. Katzke, Giovanna Masala, Sabina Sieri, Carlotta Sacerdote, Salvatore Panico, Raul Zamora‐Ros, Maria‐Jose Sánchez, José María Huerta, Marcela Guevara, Ana Vinagre‐Aragon, Paolo Vineis, Christina M. Lill, Gary W. Miller, Susan Peters, Roel Vermeulen   +20 more
wiley   +1 more source

Comment on Dashtipour et al. Dysphagia and Muscle Weakness Secondary to Botulinum Toxin Type A Treatment of Cervical Dystonia: A Drug Class Analysis of Prescribing Information. <i>Toxins</i> 2024, <i>16</i>, 442. [PDF]

Toxins (Basel)
Trosch R, Parreirinha D, Proeschel S.
europepmc   +1 more source

Dysphagia lusoria in children

, 1996
Baruch Klin, Z. Tauber, Amir Peer, Efrat Broide, I. Vinograd, A Bass   +5 more
openalex   +1 more source

Phosphatidylethanolamines are the Main Lipid Class Altered in Red Blood Cells from Patients with VPS13A Disease/Chorea‐Acanthocytosis

Movement Disorders, Volume 40, Issue 3, Page 544-549, March 2025.
VPS13A disease has become paradigmatic for a new pathophysiological concept in neurodegeneration: disturbed bulk lipid transfer at membrane contact sites. VPS13A is a bridge‐like lipid transfer protein. Loss of VPS13A function leads to deformed red blood cells (RBCs), acanthocytes.
Kevin Peikert, Adrian Spranger, Gabriel Miltenberger‐Miltenyi, Hannes Glaß, Björn Falkenburger, Christian Klose, Donatienne Tyteca, Andreas Hermann   +7 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

Endoscopic and videofluoroscopic evaluations of swallowing for dysphagia: A systematic review. [PDF]

Braz J Otorhinolaryngol
Ferrari de Castro MA, Dedivitis RA, Luongo de Matos L, Baraúna JC, Kowalski LP, de Carvalho Moura K, Herman Partezani D.   +6 more
europepmc   +1 more source

Patients with Allan‐Herndon‐Dudley Syndrome (MCT8 Deficiency) Display Symptoms of Parkinsonism in Childhood and Respond to Levodopa/Carbidopa Treatment

Movement Disorders, EarlyView.
Abstract Background Patients with mutations in the monocarboxylate transporter 8 (MCT8, SLC16A2) suffer from X‐linked recessive Allan‐Herndon‐Dudley syndrome (AHDS), which is characterized by developmental delay and a severe movement disorder. Current trials using thyroid hormone derivatives to overcome the transporter defect have failed to achieve ...
Nina‐Maria Wilpert, Angela L. Hewitt, Roser Pons, Marie‐Thérèse Henke, Andrea Dell'Orco, Martin Bauer, Christiane Grolik, Stephan Menz, Monika Wahle, Annika Zink, Alessandro Prigione, Christina Reinauer, Catharina Lange, Christian Furth, Knut Brockmann, Sabine Jung‐Klawitter, Stine Christ, Angela M. Kaindl, Anna Tietze, Heiko Krude, Thomas Opladen, Markus Schuelke   +21 more
wiley   +1 more source