Comeau AM - Search Results

1

Identification of an infant with severe combined immunodeficiency by newborn screening.

Hale JE, Bonilla FA, Pai SY, Gerstel-Thompson JL, Notarangelo LD, Eaton RB, Comeau AM. Hale JE, et al. Among authors: comeau am. J Allergy Clin Immunol. 2010 Nov;126(5):1073-4. doi: 10.1016/j.jaci.2010.08.043. Epub 2010 Oct 8. J Allergy Clin Immunol. 2010. PMID: 20933257 No abstract available.

2

Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.

Zytkovicz TH, Fitzgerald EF, Marsden D, Larson CA, Shih VE, Johnson DM, Strauss AW, Comeau AM, Eaton RB, Grady GF. Zytkovicz TH, et al. Among authors: comeau am. Clin Chem. 2001 Nov;47(11):1945-55. Clin Chem. 2001. PMID: 11673361

3

Successes of newborn screening programs.

Comeau AM, Eaton RB. Comeau AM, et al. Science. 2002 Jan 4;295(5552):44-5. doi: 10.1126/science.295.5552.44c. Science. 2002. PMID: 11780647 No abstract available.

4

Newborn screening: new developments in a proven field.

Eaton RB, Comeau AM, Zytkovicz TH, Larson C. Eaton RB, et al. Among authors: comeau am. Clin Lab Sci. 2002 Fall;15(4):239-44. Clin Lab Sci. 2002. PMID: 12776784 No abstract available.

5

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

6

Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections.

Comeau AM, Parad RB, Dorkin HL, Dovey M, Gerstle R, Haver K, Lapey A, O'Sullivan BP, Waltz DA, Zwerdling RG, Eaton RB. Comeau AM, et al. Pediatrics. 2004 Jun;113(6):1573-81. doi: 10.1542/peds.113.6.1573. Pediatrics. 2004. PMID: 15173476

7

Challenges in implementing a successful newborn cystic fibrosis screening program.

Comeau AM, Parad R, Gerstle R, O'Sullivan BP, Dorkin HL, Dovey M, Haver K, Martin T, Eaton RB. Comeau AM, et al. J Pediatr. 2005 Sep;147(3 Suppl):S89-93. doi: 10.1016/j.jpeds.2005.08.006. J Pediatr. 2005. PMID: 16202791 Review.

8

Communications systems and their models: Massachusetts parent compliance with recommended specialty care after positive cystic fibrosis newborn screening result.

Comeau AM, Parad R, Gerstle R, O'Sullivan BP, Dorkin HL, Dovey M, Haver K, Martin T, Eaton RB. Comeau AM, et al. J Pediatr. 2005 Sep;147(3 Suppl):S98-100. doi: 10.1016/j.jpeds.2005.08.007. J Pediatr. 2005. PMID: 16202793

9

Newborn screening showing decreasing incidence of cystic fibrosis.

Hale JE, Parad RB, Comeau AM. Hale JE, et al. Among authors: comeau am. N Engl J Med. 2008 Feb 28;358(9):973-4. doi: 10.1056/NEJMc0707530. N Engl J Med. 2008. PMID: 18305279 No abstract available.

10

Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening.

Hsu HW, Zytkovicz TH, Comeau AM, Strauss AW, Marsden D, Shih VE, Grady GF, Eaton RB. Hsu HW, et al. Among authors: comeau am. Pediatrics. 2008 May;121(5):e1108-14. doi: 10.1542/peds.2007-1993. Pediatrics. 2008. PMID: 18450854

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