Results 81 to 90 of about 68,413,542 (286)

Onasemnogene Abeparvovec in Patients With SMA: Interim Results of the RESTORE Registry in Japan

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective There are limited real‐world data regarding the safety and effectiveness of onasemnogene abeparvovec (OA; Zolgensma) infusion, a one‐time gene replacement therapy, for Japanese patients with spinal muscular atrophy (SMA). We aimed to improve understanding of the real‐world outcomes for OA in Japan.
Kayoko Saito, Kamal Benguerba, Ken Tsuchida, Kazushige Yazawa, Isao Tsumiyama, Hiromitsu Kayama, Sandra P. Reyna, Farid Khan, Richard S. Finkel   +8 more
wiley   +1 more source

Clinical and Modifiable Factors Associated With Disability and Relapse in MOGAD: A Multicentre Cohort Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Factors associated with relapse course and disability in myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) remain incompletely understood. Objectives To identify clinical and modifiable factors associated with relapse and disability in MOGAD. Methods In this ambispective multicentre cohort study using data from
Yingtao Wang, Shaoxin Tao, Qiujia Wang, Xiaoyu Xu, Hui Yao, Zheng Liu, Dawei Li, Zhandong Qiu, Jinming Han, Jiangwei Xia, Qi Wang, Jun Sun, Kai Shao, Jiao Li, Shishuang Ruan, Yi Zhong, Jun Guo, Shougang Guo, Yue Huang, Guoliang Chai, Tao Jin, Hongyu Zhou, Junwei Hao, Yinan Zhao   +23 more
wiley   +1 more source

Deep Learning Pose Estimation for Phenotyping of Co‐Occurring Hyperkinetic Movement Disorders

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To explore whether routine outpatient video combined with deep learning‐based pose estimation and clinically interpretable kinematic features can support multi‐label phenotyping of co‐occurring hyperkinetic movement disorders (HMDs).
Laura Cif, Diane Demailly, Gabriella A. Horvàth, Juan Dario Ortigoza Escobar, Nathalie Dorison, Mayté Castro Jiménez, Cécile A. Hubsch, Thomas Wirth, Gun‐Marie Hariz, Sophie Huby, Morgan Dornadic, Zohra Souei, Muhammad Mushhood Ur Rehman, Simone Hemm, Mehdi Boulaymen, Eduardo M. Moraud, Jocelyne Bloch, Xavier Vasques   +17 more
wiley   +1 more source

Section of Children and Youth with Special Health Care Needs: Who We Are and What We Do

This document, printed in Spanish, describes the mission, goals, strategies, and activities of the Section of Children and Youth with Special Health Care ...
South Carolina Department of Public Health, Section of Children and Youth with Special Health Care Needs
core   +3 more sources

Progressive Parkinsonism in PPP2R5D‐Related Neurodevelopmental Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT PPP2R5D‐related neurodevelopmental disorder (Houge–Janssens syndrome type 1) is a rare autosomal dominant condition characterized by macrocephaly, intellectual disability, and epilepsy. Progressive parkinsonism is an emerging adult phenotype that neurologists should be aware of since timely genetic diagnosis opens the door to disease‐modifying
Katerina Bernardi, Enrique Gonzalez Saez‐Diez, Joshua Rong, Beril Ay, Shabbir Merchant, Kathryn Yang, Darius Ebrahimi‐Fakhari   +6 more
wiley   +1 more source

Impact of Age on the Diagnostic Yield of Routine EEG in People With Childhood or Juvenile Absence Epilepsy: A Cross‐Sectional Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background We aimed to identify the proportion of individuals with a confirmed diagnosis of childhood absence epilepsy (CAE) or juvenile absence epilepsy (JAE) who show a negative routine EEG (rEEG), and to determine the main factors associated with this finding.
Francesco Fortunato, Alessia Giugno, Miriam Sturniolo, Enrico Fratto, Pio Zoleo, Francesca Felicia Operto, Ilaria Sammarra, Antonio Gambardella   +7 more
wiley   +1 more source

Comparing the Efficiency of Neuropsychological and Davis Method Interventions on Language Skills (Phonological, Semantic, Syntactic Skills) of Dyslexic Students

Taḥqīqāt-i ̒Ulūm-i Raftārī, 2018
Aim and Background: As one of the most common learning disabilities, dyslexia is associated with a delayed reading ability and characterized by a considerable failure in the development of vocabulary recognition skills and reading comprehension.The ...
Farzaneh Momeni Shahraki, Mokhtar Malekpour, Ahmad Abedi, Salar Faramarzi   +3 more
doaj  

اثربخشی آموزش قصه‌های مبتنی بر دیالوگ بر مهارت‌های زبانی کودکان دختر کم‌توان هوشی آموزش‌پذیر مقطع دبستان

مجله پژوهش در علوم توانبخشی, 2017
مقدمه: از مهم‌ترین مشکلات کودکان کم‌توان هوشی، محدودیت در مهارت‌های زبانی است. یکی از روش‌های پیشنهاد شده جهت ارتقای مهارت‌های زبانی، استفاده از قصه‌گویی به روش دیالوگ می‌باشد. هدف از انجام پژوهش حاضر، بررسی اثربخشی آموزش قصه‌های مبتنی بر دیالوگ بر مهارت‌
Afrooz Makarem-Nasab, Ahmad Yarmohammadian, Amir Ghamarani   +2 more
doaj   +1 more source

Special needs experiences of mothers with children with special needs

Balıkesir Üniversitesi Sosyal Bilimler Enstitüsü Dergisi
In this study, the focus is on the experiences of mothers with children with special needs, the difficulties experienced by these mothers, support needs, and social reactions. The research was designed using a qualitative method and was conducted using more than one qualitative research design.
Davut Açar, Resul Duran, Yusuf Dilbilir, Fırat Keskin, Cumhur Demiralp   +4 more
openaire   +1 more source

Academic attainment and special educational needs in extremely preterm children at 11 years of age : the EPICure Study [PDF]

, 2009
Aim: To assess academic attainment and special educational needs (SEN) in extremely preterm (EP) children in middle childhood. Methods: Of 307 EP (=25 weeks) survivors born in the UK and Ireland in 1995, 219 (71%) were re-assessed at 11 years, with a
Hennessy, Enid M., Wolke, Dieter, Johnson, Samantha J., Smith, R. (Rebecca), Trikic, Rebecca, Marlow, Neil   +5 more
core   +1 more source