Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nicola Jolleff"'
Autor:
David McCormick, Tara Clarke, Shan Tang, Rajesh Gupta, Steven L. Kugler, Lisa J. Strug, Marisa Pina, Sushma Goyal, Cigdem I. Akman, Caroline Oren, Anna B. Smith, John Trounce, Elaine Hughes, Hannah Cockerill, Steven M Wolf, John Jackman, David E. Mandelbaum, Kumudini Gomez, Colm J. McGinnity, Zaloa Agirre-Arrizubieta, Patricia McGoldrick, Nicola Jolleff, Jacqueline Taylor, Yaiza Hernández Vega, David Scott, Deb K. Pal
Publikováno v:
Epilepsy & Behavior. 53:174-179
Objective The high prevalence and impact of neurodevelopmental comorbidities in childhood epilepsy are now well known, as are the increased risks and familial aggregation of reading disability (RD) and speech sound disorder (SSD) in rolandic epilepsy
Publikováno v:
Developmental Medicine & Child Neurology. 52:27-32
AIM Worster-Drought syndrome (WDS), or congenital suprabulbar paresis, is a permanent movement disorder of the bulbar muscles causing persistent difficulties with swallowing, feeding, speech, and saliva control owing to a non-progressive disturbance
Publikováno v:
Child: Care, Health and Development. 34:223-229
Background The Communication Aids Project (CAP) was a 4-year initiative by the UK Department for Education and Skills to provide communication equipment for students who were unable to speak in order to facilitate their access to education. Each chil
Autor:
Maria Clark, Michelle Downes, Steve White, Rebecca Greenaway, Marios Kaliakatsos, Brian G. R. Neville, Nicola Jolleff, J. Helen Cross, William Harkness, Stewart Boyd
Summary Objective To determine whether multiple subpial transection in the posterior temporal lobe has an impact on long-term outcome in children who have drug-resistant Landau-Kleffner syndrome (LKS) or other “electrical status epilepticus during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10fb5f77923f455409a7553d5826c2a9
Publikováno v:
Advances in Speech Language Pathology. 8:28-33
Angelman syndrome (AS) is a neurogenetic disorder caused by maternal deletions of 15q11-13 (classic deletion), paternal uniparental disomy (UPD), imprinting defects, and point mutations or small deletions in the UBE3A gene. It has been suggested that
Autor:
Nicola Jolleff, Steve White, Rebecca Greenaway, Marios Kaliakatsos, Brian G. R. Neville, J. Helen Cross, Michelle Downes, William Harkness, Stewart Boyd, Maria Clark
Publikováno v:
Epilepsia. 57:674-675
We thank Dr. Kheder and colleagues for their letter and we are grateful for their comments.
Autor:
Neely, Desai, Ronit M, Pressler, Nicola, Jolleff, Maria, Clark, Brian, Neville, Christin, Eltze, William, Harkness, J Helen, Cross
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 10(4)
We report the case of a six-year-old boy who presented in infancy with infantile spasms and left focal seizures. An MR scan at two months was suggestive of a right parietal cortical dysplasia, although this was less apparent on repeat scan at 11 mont
Publikováno v:
Child Language Teaching and Therapy. 6:305-321
Children who are severely physically handicapped and non-speaking may be assessed for recommendation of an augmentative communica tion system. A working model of assessment, developed at the Com munication Aids Centre at The Wolfson Centre, London, i
Publikováno v:
Child: care, health and development. 24(3)
Some children with severe motor disorders have unintelligible speech, and may be recommended augmentative communication systems, such as a symbol chart or a voice output aid. The paper reports the outcome after 15–18 months for 35 children of recom
Publikováno v:
Developmental medicine and child neurology. 34(8)
SUMMARY This paper describes the organisation and procedures of the Communication Aids Centre for children at the Wolfson Centre, London, including a model for assessment and recommendation of appropriate aids, such as symbol charts, switches and spe