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Items: 1 to 20 of 190

1.

Content of communication by pediatric residents after newborn genetic screening.

Farrell MH, La Pean A, Ladouceur L.

Pediatrics. 2005 Dec;116(6):1492-8.

PMID:
16322176
2.

Initially misleading communication of carrier results after newborn genetic screening.

La Pean A, Farrell MH.

Pediatrics. 2005 Dec;116(6):1499-505.

PMID:
16322177
3.

Assessment of parental understanding by pediatric residents during counseling after newborn genetic screening.

Farrell MH, Kuruvilla P.

Arch Pediatr Adolesc Med. 2008 Mar;162(3):199-204. doi: 10.1001/archpediatrics.2007.55.

PMID:
18316655
4.

Genetic counseling and neonatal screening for cystic fibrosis: an assessment of the communication process.

Ciske DJ, Haavisto A, Laxova A, Rock LZ, Farrell PM.

Pediatrics. 2001 Apr;107(4):699-705.

PMID:
11335747
5.

Pediatric residents' use of jargon during counseling about newborn genetic screening results.

Farrell M, Deuster L, Donovan J, Christopher S.

Pediatrics. 2008 Aug;122(2):243-9. doi: 10.1542/peds.2007-2160.

PMID:
18676539
6.
7.

Pediatricians' attitudes toward expanding newborn screening.

Acharya K, Ackerman PD, Ross LF.

Pediatrics. 2005 Oct;116(4):e476-84.

PMID:
16199673
8.

Genetic counseling and risk communication services of newborn screening programs.

Farrell M, Certain L, Farrell P.

Arch Pediatr Adolesc Med. 2001 Feb;155(2):120-6.

PMID:
11177084
9.

Frequency of high-quality communication behaviors used by primary care providers of heterozygous infants after newborn screening.

Farrell MH, Christopher SA.

Patient Educ Couns. 2013 Feb;90(2):226-32. doi: 10.1016/j.pec.2012.10.024. Epub 2012 Nov 26.

10.

A pilot study to evaluate knowledge and attitudes of Illinois pediatricians toward newborn screening for sickle cell disease and cystic fibrosis.

Stark AP, Lang CW, Ross LF.

Am J Perinatol. 2011 Mar;28(3):169-76. doi: 10.1055/s-0030-1265828. Epub 2010 Sep 9.

PMID:
20830657
11.

A systematic review of the effects of disclosing carrier results generated through newborn screening.

Hayeems RZ, Bytautas JP, Miller FA.

J Genet Couns. 2008 Dec;17(6):538-49. doi: 10.1007/s10897-008-9180-1. Epub 2008 Oct 28. Review.

PMID:
18956236
12.

Disclosing to parents newborn carrier status identified by routine blood spot screening.

Oliver S, Dezateux C, Kavanagh J, Lempert T, Stewart R.

Cochrane Database Syst Rev. 2004 Oct 18;(4):CD003859. Review.

PMID:
15495068
13.

Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.

Bailey DB Jr, Skinner D, Davis AM, Whitmarsh I, Powell C.

Pediatrics. 2008 Mar;121(3):e693-704. doi: 10.1542/peds.2007-0820. Review.

PMID:
18310190
14.

Improving the quality of physician communication with rapid-throughput analysis and report cards.

Farrell MH, Christopher SA, La Pean Kirschner A, Roedl SJ, O'Tool FO, Ahmad NY, Farrell PM.

Patient Educ Couns. 2014 Nov;97(2):248-55. doi: 10.1016/j.pec.2014.07.028. Epub 2014 Aug 28.

15.

Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening.

Ulph F, Cullinan T, Qureshi N, Kai J.

Eur J Hum Genet. 2015 Apr;23(4):459-65. doi: 10.1038/ejhg.2014.126. Epub 2014 Jul 9.

16.

Information flow after a positive newborn screening for cystic fibrosis.

Dillard JP, Tluczek A.

J Pediatr. 2005 Sep;147(3 Suppl):S94-7. Review.

PMID:
16202792
17.

Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?

Scotet V, Audrézet MP, Roussey M, Rault G, Dirou-Prigent A, Journel H, Moisan-Petit V, Storni V, Férec C.

Pediatrics. 2006 Nov;118(5):e1523-9. Epub 2006 Oct 2.

PMID:
17015492
18.

Genetic counseling following the detection of hemoglobinopathy trait on the newborn screen is well received, improves knowledge, and relieves anxiety.

Kladny B, Williams A, Gupta A, Gettig EA, Krishnamurti L.

Genet Med. 2011 Jul;13(7):658-61. doi: 10.1097/GIM.0b013e31821435f7.

PMID:
21546841
19.

Improving communication between doctors and parents after newborn screening.

Farrell MH, Christopher SA, Tluczek A, Kennedy-Parker K, La Pean A, Eskra K, Collins J, Hoffman G, Panepinto J, Farrell PM.

WMJ. 2011 Oct;110(5):221-7.

20.

Infant hearing screening: stakeholder recommendations for parent-centered communication.

Arnold CL, Davis TC, Humiston SG, Bocchini JA Jr, Bass PF 3rd, Bocchini A, Kennen EM, White K, Forsman I.

Pediatrics. 2006 May;117(5 Pt 2):S341-54.

PMID:
16735261

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