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Items: 1 to 20 of 98

1.

Speech and language in bilateral perisylvian polymicrogyria: a systematic review.

Braden RO, Leventer RJ, Jansen A, Scheffer IE, Morgan AT.

Dev Med Child Neurol. 2019 Jan 25. doi: 10.1111/dmcn.14153. [Epub ahead of print] Review.

PMID:
30680716
2.

[Characterization of the linguistic profile of a family with Perisylvian Syndrome].

de Oliveira EP, Guerreiro MM, Guimarães CA, Brandão-Almeida IL, Montenegro MA, Cendes F, Hage SR.

Pro Fono. 2005 Apr-Dec;17(3):393-402. Portuguese.

PMID:
16389796
3.

Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study.

Mirzaa GM, Conti V, Timms AE, Smyser CD, Ahmed S, Carter M, Barnett S, Hufnagel RB, Goldstein A, Narumi-Kishimoto Y, Olds C, Collins S, Johnston K, Deleuze JF, Nitschké P, Friend K, Harris C, Goetsch A, Martin B, Boyle EA, Parrini E, Mei D, Tattini L, Slavotinek A, Blair E, Barnett C, Shendure J, Chelly J, Dobyns WB, Guerrini R.

Lancet Neurol. 2015 Dec;14(12):1182-95. doi: 10.1016/S1474-4422(15)00278-1. Epub 2015 Oct 29.

4.

Bilateral posterior parietal polymicrogyria: a mild form of congenital bilateral perisylvian syndrome?

Montenegro MA, Guerreiro MM, Lopes-Cendes I, Cendes F.

Epilepsia. 2001 Jul;42(7):845-9.

5.

Cognitive functioning in bilateral perisylvian polymicrogyria (BPP): clinical and radiological correlations.

Jansen AC, Leonard G, Bastos AC, Esposito-Festen JE, Tampieri D, Watkins K, Andermann F, Andermann E.

Epilepsy Behav. 2005 May;6(3):393-404.

PMID:
15820349
6.

The syndrome of perisylvian polymicrogyria with congenital arthrogryposis.

Poduri A, Chitsazzadeh V, D'Arrigo S, Fedrizzi E, Pantaleoni C, Riva D, Busse C, Küster H, Duplessis A, Gaitanis J, Sahin M, Garganta C, Topcu M, Dies KA, Barry BJ, Partlow J, Barkovich AJ, Walsh CA, Chang BS.

Brain Dev. 2010 Aug;32(7):550-5. doi: 10.1016/j.braindev.2009.08.005. Epub 2009 Sep 13.

7.

Verbal and gestural communication in children with bilateral perisylvian polymicrogyria.

Saletti V, Bulgheroni S, D'Incerti L, Franceschetti S, Molteni B, Airaghi G, Pantaleoni C, D'Arrigo S, Riva D.

J Child Neurol. 2007 Sep;22(9):1090-8.

PMID:
17890406
8.

FOXP2-Related Speech and Language Disorders.

Morgan A, Fisher SE, Scheffer I, Hildebrand M.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2016 Jun 23 [updated 2017 Feb 2].

9.

Congenital perisylvian dysfunction - is it a spectrum?

Clark M, Chong WK, Cox T, Neville BG.

Dev Med Child Neurol. 2010 Jan;52(1):33-9. doi: 10.1111/j.1469-8749.2009.03348.x. Epub 2009 Jun 22.

10.

Interventions for childhood apraxia of speech.

Morgan AT, Murray E, Liégeois FJ.

Cochrane Database Syst Rev. 2018 May 30;5:CD006278. doi: 10.1002/14651858.CD006278.pub3. Review.

PMID:
29845607
11.

Screening for speech and language delay in preschool children: systematic evidence review for the US Preventive Services Task Force.

Nelson HD, Nygren P, Walker M, Panoscha R.

Pediatrics. 2006 Feb;117(2):e298-319. Review. Erratum in: Pediatrics. 2006 Jun;117(6):2336-7.

PMID:
16452337
12.

Communication interventions for autism spectrum disorder in minimally verbal children.

Brignell A, Chenausky KV, Song H, Zhu J, Suo C, Morgan AT.

Cochrane Database Syst Rev. 2018 Nov 5;11:CD012324. doi: 10.1002/14651858.CD012324.pub2.

PMID:
30395694
13.

Speech and language in children with Klinefelter syndrome.

St John M, Ponchard C, van Reyk O, Mei C, Pigdon L, Amor DJ, Morgan AT.

J Commun Disord. 2019 Mar - Apr;78:84-96. doi: 10.1016/j.jcomdis.2019.02.003. Epub 2019 Feb 12.

PMID:
30822601
14.

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.

Eur J Hum Genet. 2018 Jan;26(1):75-84. doi: 10.1038/s41431-017-0035-9. Epub 2017 Dec 11.

16.

Speech and language therapy interventions for children with primary speech and language delay or disorder.

Law J, Garrett Z, Nye C.

Cochrane Database Syst Rev. 2003;(3):CD004110. Review.

PMID:
12918003
17.

Congenital polymicrogyria including the perisylvian region in early childhood.

Takano T, Matsuwake K, Yoshioka S, Takeuchi Y.

Congenit Anom (Kyoto). 2010 Mar;50(1):64-7. doi: 10.1111/j.1741-4520.2009.00253.x.

PMID:
20201970
18.

Treatment for speech disorder in Friedreich ataxia and other hereditary ataxia syndromes.

Vogel AP, Folker J, Poole ML.

Cochrane Database Syst Rev. 2014 Oct 28;(10):CD008953. doi: 10.1002/14651858.CD008953.pub2. Review.

PMID:
25348587
19.

Visual-motor integration performance in children with severe specific language impairment.

Nicola K, Watter P.

Child Care Health Dev. 2016 Sep;42(5):742-9. doi: 10.1111/cch.12365. Epub 2016 Jun 12.

PMID:
27291941
20.

Non-speech oral motor treatment for children with developmental speech sound disorders.

Lee AS, Gibbon FE.

Cochrane Database Syst Rev. 2015 Mar 25;(3):CD009383. doi: 10.1002/14651858.CD009383.pub2. Review.

PMID:
25805060

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