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Items: 1 to 20 of 42

1.

Perceptual and acoustic reliability estimates for the Speech Disorders Classification System (SDCS).

Shriberg LD, Fourakis M, Hall SD, Karlsson HB, Lohmeier HL, McSweeny JL, Potter NL, Scheer-Cohen AR, Strand EA, Tilkens CM, Wilson DL.

Clin Linguist Phon. 2010 Oct;24(10):825-46. doi: 10.3109/02699206.2010.503007.

2.

Extensions to the Speech Disorders Classification System (SDCS).

Shriberg LD, Fourakis M, Hall SD, Karlsson HB, Lohmeier HL, McSweeny JL, Potter NL, Scheer-Cohen AR, Strand EA, Tilkens CM, Wilson DL.

Clin Linguist Phon. 2010 Oct;24(10):795-824. doi: 10.3109/02699206.2010.503006.

3.

Long-term speech and language developmental issues among children with Duarte galactosemia.

Powell KK, Van Naarden Braun K, Singh RH, Shapira SK, Olney RS, Yeargin-Allsopp M.

Genet Med. 2009 Dec;11(12):874-9. doi: 10.1097/GIM.0b013e3181c0c38d.

PMID:
19904210
4.

A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT).

Shriberg LD, Lohmeier HL, Campbell TF, Dollaghan CA, Green JR, Moore CA.

J Speech Lang Hear Res. 2009 Oct;52(5):1189-212. doi: 10.1044/1092-4388(2009/08-0047). Epub 2009 Jul 27.

5.

Outcomes of siblings with classical galactosemia.

Hughes J, Ryan S, Lambert D, Geoghegan O, Clark A, Rogers Y, Hendroff U, Monavari A, Twomey E, Treacy EP.

J Pediatr. 2009 May;154(5):721-6. doi: 10.1016/j.jpeds.2008.11.052. Epub 2009 Feb 1.

PMID:
19181333
6.

Treatment of childhood apraxia of speech: clinical decision making in the use of nonspeech oral motor exercises.

McCauley RJ, Strand EA.

Semin Speech Lang. 2008 Nov;29(4):284-93. doi: 10.1055/s-0028-1103392. Epub 2008 Dec 4. Review.

PMID:
19058115
7.

Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS).

Shriberg LD, Jakielski KJ, El-Shanti H.

Am J Med Genet A. 2008 Sep 1;146A(17):2227-33. doi: 10.1002/ajmg.a.32363.

PMID:
18671280
8.

Correlates of language impairment in children with galactosaemia.

Potter NL, Lazarus JA, Johnson JM, Steiner RD, Shriberg LD.

J Inherit Metab Dis. 2008 Aug;31(4):524-32. doi: 10.1007/s10545-008-0877-y. Epub 2008 Jul 12.

9.

The genetic bases of speech sound disorders: evidence from spoken and written language.

Lewis BA, Shriberg LD, Freebairn LA, Hansen AJ, Stein CM, Taylor HG, Iyengar SK.

J Speech Lang Hear Res. 2006 Dec;49(6):1294-312. Review.

PMID:
17197497
10.

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.

Feuk L, Kalervo A, Lipsanen-Nyman M, Skaug J, Nakabayashi K, Finucane B, Hartung D, Innes M, Kerem B, Nowaczyk MJ, Rivlin J, Roberts W, Senman L, Summers A, Szatmari P, Wong V, Vincent JB, Zeesman S, Osborne LR, Cardy JO, Kere J, Scherer SW, Hannula-Jouppi K.

Am J Hum Genet. 2006 Nov;79(5):965-72. Epub 2006 Sep 27.

11.

Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.

Shriberg LD, Ballard KJ, Tomblin JB, Duffy JR, Odell KH, Williams CA.

J Speech Lang Hear Res. 2006 Jun;49(3):500-25.

PMID:
16787893
12.

Speech sound disorder influenced by a locus in 15q14 region.

Stein CM, Millard C, Kluge A, Miscimarra LE, Cartier KC, Freebairn LA, Hansen AJ, Shriberg LD, Taylor HG, Lewis BA, Iyengar SK.

Behav Genet. 2006 Nov;36(6):858-68. Epub 2006 Jun 20.

PMID:
16786424
13.

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

Zeesman S, Nowaczyk MJ, Teshima I, Roberts W, Cardy JO, Brian J, Senman L, Feuk L, Osborne LR, Scherer SW.

Am J Med Genet A. 2006 Mar 1;140(5):509-14.

PMID:
16470794
14.

The eloquent ape: genes, brains and the evolution of language.

Fisher SE, Marcus GF.

Nat Rev Genet. 2006 Jan;7(1):9-20. Review.

PMID:
16369568
15.

Research for newborn screening: developing a national framework.

Botkin JR.

Pediatrics. 2005 Oct;116(4):862-71.

PMID:
16199695
16.

A subtype of speech delay associated with developmental psychosocial involvement.

Hauner KK, Shriberg LD, Kwiatkowski J, Allen CT.

J Speech Lang Hear Res. 2005 Jun;48(3):635-50.

PMID:
16197278
17.

An updated review of the long-term neurological effects of galactosemia.

Ridel KR, Leslie ND, Gilbert DL.

Pediatr Neurol. 2005 Sep;33(3):153-61. Review.

PMID:
16087312
18.

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.

MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE.

Am J Hum Genet. 2005 Jun;76(6):1074-80. Epub 2005 Apr 22.

19.

A diagnostic marker for childhood apraxia of speech: the coefficient of variation ratio.

Shriberg LD, Green JR, Campbell TF, McSweeny JL, Scheer AR.

Clin Linguist Phon. 2003 Oct-Nov;17(7):575-95.

PMID:
14608800
20.

A diagnostic marker for childhood apraxia of speech: the lexical stress ratio.

Shriberg LD, Campbell TF, Karlsson HB, Brown RL, McSweeny JL, Nadler CJ.

Clin Linguist Phon. 2003 Oct-Nov;17(7):549-74.

PMID:
14608799

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