Results 221 to 230 of about 12,086 (333)

Developmental deglutition and intrinsic tongue muscle maturation phenotypes in the Ts65Dn mouse model of Down syndrome. [PDF]

Front Neurol
Glass TJ, Chatwin BA, Fisher EH, Hang KK, Yang Q, Brutto R, Waghray R, Connor NP.   +7 more
europepmc   +1 more source

Validation of Clinical Observations of Mastication in Persons with ALS [PDF]

, 2016

core   +1 more source

A New Phenotype–Genotype Correlation for FIG4 and Parkinson's Disease

Movement Disorders Clinical Practice, EarlyView.
Iro Boura, Panayiotis Mitsias, Sofia Erimaki, Efrosini Papadaki, Cleanthe Spanaki   +4 more
wiley   +1 more source

Stridor Is an Independent Risk Factor for Mortality and Disease Progression in Patients with Multiple System Atrophy

Movement Disorders, EarlyView.
Abstract Background and aim Stridor and sleep apnea syndrome (SAS) are common in multiple system atrophy (MSA). Retrospective cohort studies have yielded conflicting results regarding the consequences of stridor and SAS on the disease course. This study aimed to assess the prognostic significance of stridor and SAS, as well as the potential survival ...
Pauline Dodet, Cecile Proust‐Lima, Federico Sirna, David Bendetowicz, Giulia Lazzeri, Rachel Debs, Anna Delamarre, Margaux Dunoyer, Margherita Fabbri, Claire Georges, Imad Ghorayeb, David Grabli, Cécile Londner, Anne Pavy‐Le Traon, Maxime Patout, Olivier Rascol, Isabelle Arnulf, Alexandra Foubert‐Samier, Wassilios G. Meissner   +18 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

Early Onset Dystonia, Parkinsonism, and Spasticity in Siblings with VAC14‐Associated Neurodegeneration: A Case Report and Literature Review

Movement Disorders Clinical Practice, EarlyView.
Rebecca Lindsay, Sangeetha Yoganathan, Wei Kang Lim, Pradeep Krishnan, Asif Doja, Sunita Venkateswaran, Julie Richer, Sara Breitbart, Nicole S.Y. Liang, Alfonso Fasano, George M. Ibrahim, Carolina Gorodetsky   +11 more
wiley   +1 more source

Analysis of a Modified Version of the Inventory of Non‐Ataxia Signs Over 12 Years in Patients with Friedreich's Ataxia in the EFACTS Study

Movement Disorders, EarlyView.
Abstract Background Friedreich's ataxia is a rare, neurodegenerative, multisystem disorder. While ataxia is a hallmark, non‐ataxia signs, including muscle weakness, spasticity, and dysphagia are equally disabling. The Inventory of Non‐Ataxia Signs (INAS) is a symptom list transformable to a 16‐item count.
Stella Andrea Lischewski, Imis Dogan, Paola Giunti, Michael H. Parkinson, Caterina Mariotti, Alexandra Durr, Claire Ewenczyk, Sylvia Boesch, Wolfgang Nachbauer, Thomas Klopstock, Claudia Stendel, Francisco Javier Rodríguez de Rivera Garrido, Ludger Schöls, Zofia Fleszar, Thomas Klockgether, Marcus Grobe‐Einsler, Ilaria Giordano, Myriam Rai, Massimo Pandolfo, Heike Jacobi, Ralf‐Dieter Hilgers, Jörg B. Schulz, Kathrin Reetz, on behalf of the EFACTS Study Group   +23 more
wiley   +1 more source

Aggressive Mucormycosis with Extensive Craniofacial Involvement: A Case Report of Radical Surgical Management and Prosthetic Rehabilitation. [PDF]

Reports (MDPI)
Marzi Manfroni A, Arcuri F, Spinzia A, Sako M, Bianchi B, Laganà F.   +5 more
europepmc   +1 more source

Motion Correction in High‐Resolution 3D Brain MRSI Without Water and Lipid Suppression

Magnetic Resonance in Medicine, EarlyView.
ABSTRACT Purpose To develop an effective method for correcting head motion in high‐resolution, non‐water‐suppressed MRSI. Methods MRSI scans are susceptible to subject motion due to the long data acquisition time required for sufficient spatial‐spectral encodings.
Ziwen Ke, Yibo Zhao, Rong Guo, Yudu Li, Wen Jin, Huixiang Zhuang, Yao Li, Zhi‐Pei Liang   +7 more
wiley   +1 more source

[Aicardi-Goutières syndrome with atypical presentation: RNASEH2B gene mutation in an infant without microcephaly or intracranial calcifications (a case report)]. [PDF]

Pan Afr Med J
Iddir S, Lounis B, Ouarab M, Guendoud T, Feghoul C, Benarab K, Hamzaoui A, Benssadi N.   +7 more
europepmc   +1 more source