Results 321 to 330 of about 121,688 (385)

Analysis of Eye Movements in Adults with Spinal Muscular Atrophy. [PDF]

Medicina (Kaunas)
Krivošík M, Košutzká Z, Šaling M, Boleková V, Brauneckerová R, Gábor M, Valkovič P.   +6 more
europepmc   +1 more source

Operative treatment of severe scoliosis and pelvic obliquity in patients with spinal muscular atrophy: assessment of outcomes and complications. [PDF]

Orphanet J Rare Dis
Sun H, Huang Y, Dong Y, Wang Z, Zhao J, Huang X, Chen W, Shen J.   +7 more
europepmc   +1 more source

Neurodegenerative and Neurodevelopmental Roles for Bulk Lipid Transporters VPS13A and BLTP2

Movement Disorders, EarlyView.
Abstract Background Bridge‐like lipid transfer proteins (BLTPs) mediate bulk lipid transport at membrane contact sites. Mutations in BLTPs are linked to both early‐onset neurodevelopmental and later‐onset neurodegenerative diseases, including movement disorders.
Sarah D. Neuman, Rajan S. Thakur, Scott J. Gratz, Kate M. O'Connor‐Giles, Arash Bashirullah   +4 more
wiley   +1 more source

Bulbar-Onset Amyotrophic Lateral Sclerosis Unmasked by General Anesthesia: A Case Report. [PDF]

Cureus
Bouabdallaoui A, Taouihar S, Yahya N, Adali N, Nassik H.   +4 more
europepmc   +1 more source

Corticospinal Tract Development, Evolution, and Skilled Movements

Movement Disorders, EarlyView.
Abstract The evolution of the corticospinal tract (CST) is closely linked to the development of skilled voluntary movements in mammals. The main evolutionary divergence concerns the position of the CST within the spinal cord white matter and its postsynaptic targets in the grey matter.
Emmanuel Roze, Caroline Dubacq, Quentin Welniarz   +2 more
wiley   +1 more source

Hirayama's Disease: About a Clinical Observation. [PDF]

Cureus
Touiti B, Souirti Z.
europepmc   +1 more source

Rare GNAO1 Variant Presenting with Deep Brain Stimulation‐Responsive Jaw‐Opening Dystonia

Movement Disorders Clinical Practice, EarlyView.
Fabian Maass, Saskia Biskup, Vesna Malinova, Christiane Weinrich, Christoph van Riesen   +4 more
wiley   +1 more source

Genetic Risk Factors in Normal Pressure Hydrocephalus: What We Know and What Is Next

Movement Disorders, EarlyView.
Abstract Knowledge of the genetic factors in normal pressure hydrocephalus (NPH) is rapidly evolving, with significant advances in recent years. We conducted a systematic review examining genetic contributions to NPH risk. Ovid Embase, Ovid Medline, Web of Science, and Cochrane Central were searched from inception through October 14, 2024, for human ...
Camila C. Piccinin, Saar Anis, Jeryl Ritzi T. Yu, Philippe A. Salles, Henry Mauricio Chaparro‐Solano, Avery Kundrick, Shelley Ivary, James Y. Liao, Sean J. Nagel, Ignacio F. Mata   +9 more
wiley   +1 more source

Neurology pioneers in Japan. [PDF]

Arq Neuropsiquiatr
Teive HAG, Coutinho L, Cardoso FEC, Tsuji S.   +3 more
europepmc   +1 more source

Adult‐Onset Dystonia‐Parkinsonism: Do Not Forget SERAC1

Movement Disorders Clinical Practice, EarlyView.
Giulia Scacciatella, Costanza Masetti, Vidal Yahya, Mauro Treddenti, Gaia Oggioni, Tommaso Bocci, Laura Campiglio, Manuela Zardoni, Chiara Rosci, Marta Pengo, Chiara Manfredi, Roberto Del Bo, Edoardo Monfrini, Alessio Di Fonzo, Maurizio Inghilleri, Alberto Priori   +15 more
wiley   +1 more source