نتائج البحث - "Townend, Gillian S"

المصدر: Townend , G S , Bartolotta , T E , Urbanowicz , A , Wandin , H & Curfs , L M G 2020 , Rett Syndrome Communication Guidelines : A handbook for therapists, educators and families . Rettsyndrome.org .

مصطلحات موضوعية: Rett syndrome, Consensus-based guidelines, Augmentative and alternative communication (AAC), Assessment, Intervention, Long term management of communication

وصف الملف: application/pdf

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4

دورية أكاديمية

A comparison of formal and informal methods for assessing language and cognition in children with Rett syndrome

المؤلفون: Ward, Callie, Chiat, Shula, Townend, Gillian S

المصدر: Ward , C , Chiat , S & Townend , G S 2021 , ' A comparison of formal and informal methods for assessing language and cognition in children with Rett syndrome ' , Research in Developmental Disabilities , vol. 114 , 103961 . https://doi.org/10.1016/j.ridd.2021.103961Test

مصطلحات موضوعية: ATTENTION, Augmentative and alternative communication, Cognitive assessment, DEVELOPMENTAL LEVEL, EYE-TRACKING, Eye tracking, FEMALES, GIRLS, NEED, Neurodevelopmental disorder, Receptive and expressive language assessment, Rett syndrome

الإتاحة: https://doi.org/10.1016/j.ridd.2021.103961Test
https://cris.maastrichtuniversity.nl/en/publications/5b05164c-3257-4334-b64d-fd878b0f134eTest

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5

دورية أكاديمية

Rett Syndrome as a Rare Disease : A European Perspective

المؤلفون: Townend, Gillian S., van Kranen, Henk J., van der Stel, Rob, van den Berg, Mariëlle, Smeets, Eric, van Waardenburg, Dick, Curfs, Leopold M.G.

المصدر: Public Health Genomics, 2015 Jan 01. 18(4), 233-236.

الوصول الحر: https://www.jstor.org/stable/26778209Test

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دورية أكاديمية

Abnormal Foot Position and Standing and Walking Ability in Rett Syndrome: an Exploratory Study

المؤلفون: Borst, Hanneke E., Townend, Gillian S., van Eck, Mirjam, Smeets, Eric, van den Berg, Mariëlle, Laan, Aleid, Curfs, Leopold M. G.

المصدر: Borst , H E , Townend , G S , van Eck , M , Smeets , E , van den Berg , M , Laan , A & Curfs , L M G 2018 , ' Abnormal Foot Position and Standing and Walking Ability in Rett Syndrome: an Exploratory Study ' , Journal of Developmental and Physical Disabilities , vol. 30 , no. 2 , pp. 281-295 . https://doi.org/10.1007/s10882-017-9585-6Test

العلاقة: https://research.vumc.nl/en/publications/6dadcda3-bf69-474c-af57-c05dac76d877Test

الإتاحة: https://doi.org/10.1007/s10882-017-9585-6Test
https://research.vumc.nl/en/publications/6dadcda3-bf69-474c-af57-c05dac76d877Test
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85039854338&origin=inwardTest
https://www.ncbi.nlm.nih.gov/pubmed/29563764Test

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7

دورية أكاديمية

Early development in Rett syndrome:the benefits and difficulties of a birth cohort approach

المؤلفون: Marschik, Peter B., Lemcke, Sanne, Einspieler, Christa, Zhang, Dajie, Bolte, Sven, Townend, Gillian S., Lauritsen, Marlene B.

المصدر: Marschik , P B , Lemcke , S , Einspieler , C , Zhang , D , Bolte , S , Townend , G S & Lauritsen , M B 2018 , ' Early development in Rett syndrome : the benefits and difficulties of a birth cohort approach ' , Developmental Neurorehabilitation , vol. 21 , no. 1 , pp. 68-72 . https://doi.org/10.1080/17518423.2017.1323970Test

مصطلحات موضوعية: Birth cohort, early development, longitudinal study, parent interviews, prodrome, Rett syndrome, FRAGILE-X-SYNDROME, PRESERVED SPEECH VARIANT, GENOTYPE-PHENOTYPE RELATIONSHIPS, PARENTS CONCERNS, YOUNG GIRLS, AUTISM, DIAGNOSIS, DISORDERS, CHILDREN, AGE

الإتاحة: https://doi.org/10.1080/17518423.2017.1323970Test
https://cris.maastrichtuniversity.nl/en/publications/6f84408e-4235-4aef-931f-b7adabec5d68Test

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8

دورية أكاديمية

MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases

المؤلفون: Townend, Gillian S., Ehrhart, Friederike, van Kranen, Henk J., Wilkinson, Mark, Jacobsen, Annika, Roos, Marco, Willighagen, Egon L., van Enckevort, David, Evelo, Chris T., Curfs, Leopold M. G.

المصدر: Townend , G S , Ehrhart , F , van Kranen , H J , Wilkinson , M , Jacobsen , A , Roos , M , Willighagen , E L , van Enckevort , D , Evelo , C T & Curfs , L M G 2018 , ' MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases ' , Human Mutation , vol. 39 , no. 7 , pp. 914-924 . https://doi.org/10.1002/humu.23542Test

مصطلحات موضوعية: databases, FAIR data, genetic variation, MECP2, phenotype, Rett syndrome, INTELLECTUAL DISABILITY, MUTATION DATABASE, GENOMIC VARIATION, HUMAN-DISEASE, VARIANTS, HUMANS, BIOINFORMATICS, RESOURCES, BIOBANKS, UPDATE