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Items: 1 to 20 of 96

1.

Deletion upstream of SALL1 producing Townes-Brocks syndrome.

Stevens CA, May KM.

Am J Med Genet A. 2016 Sep;170(9):2476-8. doi: 10.1002/ajmg.a.37786. Epub 2016 Jun 8. No abstract available.

PMID:
27277004
2.

Assessment of Drug Therapy-Related Issues in an Outpatient Heart Failure Population and the Potential Impact of Pharmacist-Driven Intervention.

Dempsey JT, Matta LS, Carter DM, Stevens CA, Stevenson LW, Desai AS, Cheng JW.

J Pharm Pract. 2016 Apr 13. pii: 0897190016641491. [Epub ahead of print]

PMID:
27080398
3.

Cerebrotendinous Xanthomatosis: A Treatable Genetic Disease Not to Be Missed.

Varman KM, Dunbar K, Usifo K, Stevens CA.

J Clin Rheumatol. 2016 Mar;22(2):92-3. doi: 10.1097/RHU.0000000000000367. No abstract available.

PMID:
26906304
4.

Are you sure the library is that way? Metacognitive monitoring of spatial judgments.

Stevens CA, Carlson RA.

J Exp Psychol Learn Mem Cogn. 2016 Jul;42(7):1034-49. doi: 10.1037/xlm0000229. Epub 2016 Feb 11.

PMID:
26866660
5.

Instance-Based Models of Metacognition in the Prisoner's Dilemma.

Stevens CA, Taatgen NA, Cnossen F.

Top Cogn Sci. 2016 Jan;8(1):322-34. doi: 10.1111/tops.12181. Epub 2016 Jan 8.

PMID:
26748585
6.

Adapting and Integrating Photovoice in a Baccalaureate Community Course to Enhance Clinical Experiential Learning.

Gallagher MR, Stevens CA.

J Nurs Educ. 2015 Nov;54(11):659-62. doi: 10.3928/01484834-20151016-09.

PMID:
26517080
7.

Dendrimer-Linked Antifreeze Proteins Have Superior Activity and Thermal Recovery.

Stevens CA, Drori R, Zalis S, Braslavsky I, Davies PL.

Bioconjug Chem. 2015 Sep 16;26(9):1908-15. doi: 10.1021/acs.bioconjchem.5b00290. Epub 2015 Aug 20.

PMID:
26267368
8.

Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.

Marchegiani S, Davis T, Tessadori F, van Haaften G, Brancati F, Hoischen A, Huang H, Valkanas E, Pusey B, Schanze D, Venselaar H, Vulto-van Silfhout AT, Wolfe LA, Tifft CJ, Zerfas PM, Zambruno G, Kariminejad A, Sabbagh-Kermani F, Lee J, Tsokos MG, Lee CC, Ferraz V, da Silva EM, Stevens CA, Roche N, Bartsch O, Farndon P, Bermejo-Sanchez E, Brooks BP, Maduro V, Dallapiccola B, Ramos FJ, Chung HY, Le Caignec C, Martins F, Jacyk WK, Mazzanti L, Brunner HG, Bakkers J, Lin S, Malicdan MC, Boerkoel CF, Gahl WA, de Vries BB, van Haelst MM, Zenker M, Markello TC.

Am J Hum Genet. 2015 Jul 2;97(1):99-110. doi: 10.1016/j.ajhg.2015.05.017. Epub 2015 Jun 25.

9.

Intestinal malrotation in Rubinstein-Taybi syndrome.

Stevens CA.

Am J Med Genet A. 2015 Oct;167A(10):2399-401. doi: 10.1002/ajmg.a.37167. Epub 2015 Jun 19.

PMID:
26097216
10.

De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay.

Chong JX, McMillin MJ, Shively KM, Beck AE, Marvin CT, Armenteros JR, Buckingham KJ, Nkinsi NT, Boyle EA, Berry MN, Bocian M, Foulds N, Uzielli ML, Haldeman-Englert C, Hennekam RC, Kaplan P, Kline AD, Mercer CL, Nowaczyk MJ, Klein Wassink-Ruiter JS, McPherson EW, Moreno RA, Scheuerle AE, Shashi V, Stevens CA, Carey JC, Monteil A, Lory P, Tabor HK, Smith JD, Shendure J, Nickerson DA; University of Washington Center for Mendelian Genomics, Bamshad MJ.

Am J Hum Genet. 2015 Mar 5;96(3):462-73. doi: 10.1016/j.ajhg.2015.01.003. Epub 2015 Feb 12.

11.

Visuomotor control of neck surface electromyography in Parkinson's disease.

Malloy JR, Valentin JC, Hands GL, Stevens CA, Langmore SE, Noordzij JP, Stepp CE.

NeuroRehabilitation. 2014;35(4):795-803. doi: 10.3233/NRE-141169.

12.

Rubinstein-Taybi Syndrome.

Stevens CA.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2002 Aug 30 [updated 2014 Aug 7].

13.

Attenuated Listeria monocytogenes reprograms M2-polarized tumor-associated macrophages in ovarian cancer leading to iNOS-mediated tumor cell lysis.

Lizotte PH, Baird JR, Stevens CA, Lauer P, Green WR, Brockstedt DG, Fiering SN.

Oncoimmunology. 2014 May 23;3:e28926. eCollection 2014.

14.

Sowing the seeds of change: social justice as praxis in undergraduate nursing education.

Mohammed SA, Cooke CL, Ezeonwu M, Stevens CA.

J Nurs Educ. 2014 Sep;53(9):488-93.

PMID:
25081331
15.

Thiol-yne adsorbates for stable, low-density, self-assembled monolayers on gold.

Stevens CA, Safazadeh L, Berron BJ.

Langmuir. 2014 Mar 4;30(8):1949-56. doi: 10.1021/la404940q. Epub 2014 Feb 19.

PMID:
24512439
16.

Implementation of a dexmedetomidine stewardship program at a tertiary academic medical center.

Blum RM, Stevens CA, Carter DM, Hussey AP, Marquis KA, Torbic H, Southard RA, Szumita PM.

Ann Pharmacother. 2013 Nov;47(11):1400-5. doi: 10.1177/1060028013504086.

PMID:
24285756
17.

Ablepharon macrostomia syndrome: A distinct genetic entity clinically related to the group of FRAS-FREM complex disorders.

Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE, McDonald-McGinn DM, Zackai EH, Wright M, van Lieshout S, Vogel MJ, van Haelst MM, Zenker M.

Am J Med Genet A. 2013 Dec;161A(12):3012-7. doi: 10.1002/ajmg.a.36119. Epub 2013 Sep 24.

PMID:
24115501
18.

Investigation of NRXN1 deletions: clinical and molecular characterization.

Dabell MP, Rosenfeld JA, Bader P, Escobar LF, El-Khechen D, Vallee SE, Dinulos MB, Curry C, Fisher J, Tervo R, Hannibal MC, Siefkas K, Wyatt PR, Hughes L, Smith R, Ellingwood S, Lacassie Y, Stroud T, Farrell SA, Sanchez-Lara PA, Randolph LM, Niyazov D, Stevens CA, Schoonveld C, Skidmore D, MacKay S, Miles JH, Moodley M, Huillet A, Neill NJ, Ellison JW, Ballif BC, Shaffer LG.

Am J Med Genet A. 2013 Apr;161A(4):717-31. doi: 10.1002/ajmg.a.35780. Epub 2013 Mar 12.

PMID:
23495017
19.

Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.

Daoud H, T├ętreault M, Gibson W, Guerrero K, Cohen A, Gburek-Augustat J, Synofzik M, Brais B, Stevens CA, Sanchez-Carpintero R, Goizet C, Naidu S, Vanderver A, Bernard G.

J Med Genet. 2013 Mar;50(3):194-7. doi: 10.1136/jmedgenet-2012-101357. Epub 2013 Jan 25.

PMID:
23355746
20.

Reward circuit connectivity relates to delay discounting in children with attention-deficit/hyperactivity disorder.

Costa Dias TG, Wilson VB, Bathula DR, Iyer SP, Mills KL, Thurlow BL, Stevens CA, Musser ED, Carpenter SD, Grayson DS, Mitchell SH, Nigg JT, Fair DA.

Eur Neuropsychopharmacol. 2013 Jan;23(1):33-45. doi: 10.1016/j.euroneuro.2012.10.015. Epub 2012 Dec 1.

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