Mei C - Search Results

1

Incidence of mutism, dysarthria and dysphagia associated with childhood posterior fossa tumour.

Mei C, Morgan AT. Mei C, et al. Childs Nerv Syst. 2011 Jul;27(7):1129-36. doi: 10.1007/s00381-011-1433-x. Epub 2011 Mar 26. Childs Nerv Syst. 2011. PMID: 21442268

2

Incidence and clinical presentation of dysarthria and dysphagia in the acute setting following paediatric traumatic brain injury.

Morgan AT, Mageandran SD, Mei C. Morgan AT, et al. Among authors: mei c. Child Care Health Dev. 2010 Jan;36(1):44-53. doi: 10.1111/j.1365-2214.2009.00961.x. Epub 2009 Mar 23. Child Care Health Dev. 2010. PMID: 19320903

3

Motor speech impairment, activity, and participation in children with cerebral palsy.

Mei C, Reilly S, Reddihough D, Mensah F, Morgan A. Mei C, et al. Int J Speech Lang Pathol. 2014 Aug;16(4):427-35. doi: 10.3109/17549507.2014.917439. Epub 2014 Jun 9. Int J Speech Lang Pathol. 2014. PMID: 24910254

4

Activities and participation of children with cerebral palsy: parent perspectives.

Mei C, Reilly S, Reddihough D, Mensah F, Green J, Pennington L, Morgan AT. Mei C, et al. Disabil Rehabil. 2015;37(23):2164-73. doi: 10.3109/09638288.2014.999164. Epub 2015 Jan 14. Disabil Rehabil. 2015. PMID: 25586796

5

Speech and language in a genotyped cohort of individuals with Kabuki syndrome.

Morgan AT, Mei C, Da Costa A, Fifer J, Lederer D, Benoit V, McMillin MJ, Buckingham KJ, Bamshad MJ, Pope K, White SM. Morgan AT, et al. Among authors: mei c. Am J Med Genet A. 2015 Jul;167(7):1483-92. doi: 10.1002/ajmg.a.37026. Epub 2015 Mar 8. Am J Med Genet A. 2015. PMID: 25755104

6

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N. Fedorenko E, et al. Among authors: mei c. Eur J Hum Genet. 2016 Feb;24(2):302-6. doi: 10.1038/ejhg.2015.149. Epub 2015 Jul 15. Eur J Hum Genet. 2016. PMID: 26173965 Free PMC article.

7

Language outcomes of children with cerebral palsy aged 5 years and 6 years: a population-based study.

Mei C, Reilly S, Reddihough D, Mensah F, Pennington L, Morgan A. Mei C, et al. Dev Med Child Neurol. 2016 Jun;58(6):605-11. doi: 10.1111/dmcn.12957. Epub 2015 Nov 14. Dev Med Child Neurol. 2016. PMID: 26566585 Free article.

8

A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.

Fedorenko E, Morgan A, Murray E, Cardinaux A, Mei C, Tager-Flusberg H, Fisher SE, Kanwisher N. Fedorenko E, et al. Among authors: mei c. Eur J Hum Genet. 2016 Feb;24(2):310. doi: 10.1038/ejhg.2015.230. Eur J Hum Genet. 2016. PMID: 26763793 Free PMC article. No abstract available.

9

Who to Refer for Speech Therapy at 4 Years of Age Versus Who to "Watch and Wait"?

Morgan A, Ttofari Eecen K, Pezic A, Brommeyer K, Mei C, Eadie P, Reilly S, Dodd B. Morgan A, et al. Among authors: mei c. J Pediatr. 2017 Jun;185:200-204.e1. doi: 10.1016/j.jpeds.2017.02.059. Epub 2017 Mar 23. J Pediatr. 2017. PMID: 28343655

10

Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia.

Morgan AT, Haaften LV, van Hulst K, Edley C, Mei C, Tan TY, Amor D, Fisher SE, Koolen DA. Morgan AT, et al. Among authors: mei c. Eur J Hum Genet. 2018 Jan;26(1):75-84. doi: 10.1038/s41431-017-0035-9. Epub 2017 Dec 11. Eur J Hum Genet. 2018. PMID: 29225339 Free PMC article.

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