Search details
1.
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40.
Brain
; 146(12): 5086-5097, 2023 12 01.
Article
in English
| MEDLINE | ID: mdl-37977818
2.
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2.
J Med Genet
; 60(6): 597-607, 2023 06.
Article
in English
| MEDLINE | ID: mdl-36328423
3.
Does vaping affect the taste and smell perception? An exploratory study with New Zealand young adults.
Appetite
; 195: 107236, 2024 04 01.
Article
in English
| MEDLINE | ID: mdl-38307298
4.
Nurses' use of 'wellness' supplements during the COVID-19 pandemic in the United States.
J Adv Nurs
; 2024 Mar 21.
Article
in English
| MEDLINE | ID: mdl-38515173
5.
Pediatric healthcare professionals' attitudes and beliefs about weight stigma: A descriptive study.
J Pediatr Nurs
; 75: 64-71, 2024.
Article
in English
| MEDLINE | ID: mdl-38103459
6.
Atypical development of Broca's area in a large family with inherited stuttering.
Brain
; 145(3): 1177-1188, 2022 04 29.
Article
in English
| MEDLINE | ID: mdl-35296891
7.
Population-level policy recommendations for the prevention of disordered weight control behaviors: A scoping review.
Int J Eat Disord
; 56(8): 1463-1479, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37096990
8.
Dorsal language stream anomalies in an inherited speech disorder.
Brain
; 142(4): 966-977, 2019 04 01.
Article
in English
| MEDLINE | ID: mdl-30796815
9.
Speech in children with cerebral palsy.
Dev Med Child Neurol
; 62(12): 1374-1382, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32588921
10.
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of Speech.
Folia Phoniatr Logop
; 71(5-6): 203-215, 2019.
Article
in English
| MEDLINE | ID: mdl-31330526
11.
Risk factors associated with unintentional house fire incidents, injuries and deaths in high-income countries: a systematic review.
Inj Prev
; 23(2): 131-137, 2017 04.
Article
in English
| MEDLINE | ID: mdl-28119340
12.
All Wales Injury Surveillance System revised: development of a population-based system to evaluate single-level and multilevel interventions.
Inj Prev
; 22 Suppl 1: i50-5, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26658339
13.
New genes for focal epilepsies with speech and language disorders.
Curr Neurol Neurosci Rep
; 15(6): 35, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25921602
14.
Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants.
Neurol Genet
; 10(2): e200129, 2024 Apr.
Article
in English
| MEDLINE | ID: mdl-38715655
15.
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria.
Am J Med Genet A
; 161A(9): 2321-6, 2013 Sep.
Article
in English
| MEDLINE | ID: mdl-23918746
16.
Clinical genetic study of the epilepsy-aphasia spectrum.
Epilepsia
; 54(2): 280-7, 2013 Feb.
Article
in English
| MEDLINE | ID: mdl-23294109
17.
Modification of the home environment for the reduction of injuries.
Cochrane Database Syst Rev
; (2): CD003600, 2011 Feb 16.
Article
in English
| MEDLINE | ID: mdl-21328262
18.
Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families.
J Med Genet
; 47(3): 211-6, 2010 Mar.
Article
in English
| MEDLINE | ID: mdl-19752159
19.
Erratum to: New Genes for Focal Epilepsies with Speech and Language Disorders.
Curr Neurol Neurosci Rep
; 15(8): 55, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-26096512
20.
Self-harm presentation across healthcare settings by sex in young people: an e-cohort study using routinely collected linked healthcare data in Wales, UK.
Arch Dis Child
; 105(4): 347-354, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31611193