Comeau AM - Search Results

1

Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation.

Kemper AR, Brosco J, Comeau AM, Green NS, Grosse SD, Jones E, Kwon JM, Lam WK, Ojodu J, Prosser LA, Tanksley S. Kemper AR, et al. Among authors: comeau am. Genet Med. 2017 Jan;19(1):121-126. doi: 10.1038/gim.2016.68. Epub 2016 Jun 23. Genet Med. 2017. PMID: 27337030 Free PMC article.

2

Genetic counseling after implementation of statewide cystic fibrosis newborn screening: Two years' experience in one medical center.

Wheeler PG, Smith R, Dorkin H, Parad RB, Comeau AM, Bianchi DW. Wheeler PG, et al. Among authors: comeau am. Genet Med. 2001 Nov-Dec;3(6):411-5. doi: 10.1097/00125817-200111000-00006. Genet Med. 2001. PMID: 11715005 Free article.

3

Integration of new genetic diseases into statewide newborn screening: New England experience.

Comeau AM, Larson C, Eaton RB. Comeau AM, et al. Am J Med Genet C Semin Med Genet. 2004 Feb 15;125C(1):35-41. doi: 10.1002/ajmg.c.30001. Am J Med Genet C Semin Med Genet. 2004. PMID: 14755432

4

Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs.

Grosse SD, Boyle CA, Botkin JR, Comeau AM, Kharrazi M, Rosenfeld M, Wilfond BS; CDC. Grosse SD, et al. Among authors: comeau am. MMWR Recomm Rep. 2004 Oct 15;53(RR-13):1-36. MMWR Recomm Rep. 2004. PMID: 15483524 Free article. Review.

5

Pilot programs in newborn screening.

Pass K, Green NS, Lorey F, Sherwin J, Comeau AM. Pass K, et al. Among authors: comeau am. Ment Retard Dev Disabil Res Rev. 2006;12(4):293-300. doi: 10.1002/mrdd.20122. Ment Retard Dev Disabil Res Rev. 2006. PMID: 17183570

6

An evidence development process for newborn screening.

Perrin JM, Knapp AA, Browning MF, Comeau AM, Green NS, Lipstein EA, Metterville DR, Prosser L, Queally D, Kemper AR. Perrin JM, et al. Among authors: comeau am. Genet Med. 2010 Mar;12(3):131-4. doi: 10.1097/GIM.0b013e3181d28eb1. Genet Med. 2010. PMID: 20154629 Free article. Review. No abstract available.

7

Weighing the evidence for newborn screening for early-infantile Krabbe disease.

Kemper AR, Knapp AA, Green NS, Comeau AM, Metterville DR, Perrin JM. Kemper AR, et al. Among authors: comeau am. Genet Med. 2010 Sep;12(9):539-43. doi: 10.1097/GIM.0b013e3181e85721. Genet Med. 2010. PMID: 20601893 Free article. Review.

8

Long-term follow-up to ensure quality care of individuals diagnosed with newborn screening conditions: early experience in New England.

Sahai I, Eaton RB, Hale JE, Mulcahy EA, Comeau AM. Sahai I, et al. Among authors: comeau am. Genet Med. 2010 Dec;12(12 Suppl):S220-7. doi: 10.1097/GIM.0b013e3181fe5d37. Genet Med. 2010. PMID: 21150368 Free article.

9

Weighing the evidence for newborn screening for Hemoglobin H disease.

Kemper AR, Knapp AA, Metterville DR, Comeau AM, Green NS, Perrin JM. Kemper AR, et al. Among authors: comeau am. J Pediatr. 2011 May;158(5):780-3. doi: 10.1016/j.jpeds.2010.10.042. Epub 2010 Dec 16. J Pediatr. 2011. PMID: 21167500 Review.

10

A framework for key considerations regarding point-of-care screening of newborns.

Kemper AR, Kus CA, Ostrander RJ, Comeau AM, Boyle CA, Dougherty D, Mann MY, Botkin JR, Green NS; United States Secretary of Health and Human Services Advisory Committee. Kemper AR, et al. Among authors: comeau am. Genet Med. 2012 Dec;14(12):951-4. doi: 10.1038/gim.2012.89. Epub 2012 Aug 16. Genet Med. 2012. PMID: 22899090 Free PMC article.

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