Results 131 to 140 of about 355,304 (389)

Mechanics and Mathematical Modeling of Class III Treatment with Orthodontic Appliances with a Movable Ramp [PDF]

, 2016
Treatment of class III is a current problem in orthodontics that requires constant improvement of its methods, development of new or modifications of known methods and techniques.
Doroshenko, N. (Nataliia), Filonenko, V. (Valeriy), Flis, P. (Petro), Grigorenko, A. (Alexander), Tormakhov, M. (Mykola)   +4 more
core   +2 more sources

Electroacupuncture at HT5 + GB20 produces stronger activation effect on swallowing cortex and muscle than single points

, 2023
Xuefeng Fu, Hao Li, Wen Yang, Xuezheng Li, Lijun Lu, Hua Guo, Zhehao Wu, Kaifeng Guo, Haoming Xu, Zhen Huang   +9 more
openalex   +1 more source

Prevalence of swallowing and speech problems in daily life after chemoradiation for head and neck cancer based on cut-off scores of the patient-reported outcome measures SWAL-QOL and SHI

European Archives of Oto-Rhino-Laryngology, 2015
The objective of this study is to assess swallowing and speech outcome after chemoradiation therapy for head and neck cancer, based on the patient-reported outcome measures Swallowing Quality of Life Questionnaire (SWAL-QOL) and Speech Handicap Index ...
R. Rinkel, I. Verdonck‐de Leeuw, P. Doornaert, J. Buter, R. de Bree, J. Langendijk, Neil K. Aaronson, C. Leemans   +7 more
semanticscholar   +1 more source

Infantile‐Onset Ascending Hereditary Spastic Paraplegia due to a Homozygous ALS2 Exons 24–25 Deletion: Expanding the Genotypic Spectrum

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT We describe a novel homozygous intragenic deletion in the ALS2 gene in an 8‐year‐old boy with Infantile‐onset Ascending Hereditary Spastic Paraplegia (IAHSP) and oculomotor apraxia, thereby contributing to the expanding genetic landscape of ALS2‐related disorders.
Vito Luigi Colona, Maria Gnazzo, Silvia Genovese, Gessica Vasco, Lorena Travaglini, Maurizio Sabbadini, Marina Macchiaiolo, Francesco Nicita, Jacopo Sartorelli, Carmelo Piscopo, Enrico Castelli, Enrico Bertini, Andrea Bartuli, Antonio Novelli, Gessica Della Bella, Davide Vecchio   +15 more
wiley   +1 more source

Long-term functional outcomes and the patient perspective following altered fractionation with concomitant boost for oropharyngeal cancer [PDF]

, 2012
With no long-term data available in published research to date, this study presents details of the swallowing outcomes as well as barriers to and facilitators of oral intake and weight maintenance at 2 years after altered fractionation radiotherapy with ...
A Graeff de, A Graeff de, A Rademaker, A Trotti, AY Chen, B Cartmill, B Maciejewski, BB Mittal, Bena Cartmill, BS Bleier, CJ Semple, CL Lazarus, DF Cella, DI Rosenthal, Dietetics Association of Australia and The Speech Pathology Association of Australia Limited, DL Schwartz, E Hammerlid, E Hammerlid, E Hammerlid, EA Weymuller Jr, EC Ward, Elizabeth Ward, ER Gritz, J Bourhis, J Overgaard, J Ringash, JA Langendijk, JE Terrell, JF Fowler, JJ Caudell, JW Denham, K Bjordal, KH Yu, KK Fu, LA Newman, LB Harrison, LL D’Antonio, LM Nguyen, M Larsson, M McQuestion, MA List, MG Poulsen, MI Saunders, NP Nguyen, Petrea Cornwell, PK Ku, PR Wilson, Sandro Porceddu, TM Mekhail, U Tschiesner, U Tschiesner, W Dörr, Wendy Davidson, World Health Organisation   +53 more
core   +1 more source

Association of sarcopenia with swallowing problems, related to nutrition and activities of daily living of elderly individuals

Journal of Physical Therapy Science, 2015
[Purpose] The purpose of the current study was to clarify problems associated with swallowing, related to nutrition and activities of daily living (ADL), in elderly individuals with sarcopenia.
Hiroyasu Shiozu, M. Higashijima, T. Koga
semanticscholar   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source

Health Factors Associated With Development and Severity of Poststroke Dysphagia: An Epidemiological Investigation

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Dysphagia after stroke is common and can impact morbidity and death. The purpose of this population‐based study was to determine specific epidemiological and health risk factors that impact development of dysphagia after acute stroke.
Brittany N. Krekeler, Heidi J. P. Schieve, Jane Khoury, Lili Ding, Mary Haverbusch, Kathleen Alwell, Opeolu Adeoye, Simona Ferioloi, Jason Mackey, Daniel Woo, Matthew Flaherty, Felipe De Los Rios La Rosa, Stacie Demel, Michael Star, Elisheva Coleman, Kyle Walsh, Sabreena Slavin, Adam Jasne, Eva Mistry, Dawn Kleindorfer, Brett Kissela   +20 more
doaj   +1 more source

Journal Staff [PDF]

, 1994
Bakgrund: Dysfagi innebär avvikelser i den normala sväljningsfunktionen och är en vanlig funktionsnedsättning till följd av stroke. Tidigare studier har påvisat att incidensen av dysfagi i det akuta skedet efter stroke är 41-68 %.
Thomasson, Sofia, Wäppling, Sanna
core   +1 more source

Understanding Youth Assaults of Police Officers in Australia: A Power Threat Meaning Framework Analysis

Australian Journal of Social Issues, EarlyView.
ABSTRACT This study explores youth violence towards police officers in Australia through the Power Threat Meaning Framework (PTMF) to better understand the underlying factors contributing to such violence; focusing on power dynamics, childhood adversity, and trauma.
Dimitra Lattas, Kelly Hine, Catherine Creamer, Kelley Burton, Katelyn Davenport‐Klunder   +4 more
wiley   +1 more source