Weese-Mayer DE - Search Results

1

Crowell DH, Brooks LJ, Corwin M, Davidson-Ward S, Hunt CE, Kapuniai LE, Neuman MR, Silvestri J, Tinsley L, Weese-Mayer DE, Di Fiore J, Peucker M, Grove JS, Pearce JW; CHIME Study Group. Crowell DH, et al. J Clin Neurophysiol. 2004 Jul-Aug;21(4):290-300. doi: 10.1097/01.wnp.0000141754.03598.dc. J Clin Neurophysiol. 2004. PMID: 15509918

2

Idiopathic congenital central hypoventilation syndrome: evaluation of brain-derived neurotrophic factor genomic DNA sequence variation.

Weese-Mayer DE, Bolk S, Silvestri JM, Chakravarti A. Weese-Mayer DE, et al. Am J Med Genet. 2002 Feb 1;107(4):306-10. doi: 10.1002/ajmg.10133. Am J Med Genet. 2002. PMID: 11840487

3

Home monitoring during infancy: what is normal?

Silvestri JM, Weese-Mayer DE, Hunt CE. Silvestri JM, et al. Paediatr Respir Rev. 2002 Mar;3(1):10-7. doi: 10.1053/prrv.2002.0178. Paediatr Respir Rev. 2002. PMID: 12065177

4

An 8-month old infant discovered to be blue and not breathing during sleep.

Silvestri JM, Weese-Mayer DE, Hunt CE. Silvestri JM, et al. Paediatr Respir Rev. 2002 Mar;3(1):91-2, 95. doi: 10.1053/prrv.2002.0196. Paediatr Respir Rev. 2002. PMID: 12123227 No abstract available.

5

Idiopathic congenital central hypoventilation syndrome: the next generation.

Silvestri JM, Chen ML, Weese-Mayer DE, McQuitty JM, Carveth HJ, Nielson DW, Borowitz D, Cerny F. Silvestri JM, et al. Am J Med Genet. 2002 Sep 15;112(1):46-50. doi: 10.1002/ajmg.10819. Am J Med Genet. 2002. PMID: 12239719

6

Infant polysomnography: reliability and validity of infant arousal assessment.

Crowell DH, Kulp TD, Kapuniai LE, Hunt CE, Brooks LJ, Weese-Mayer DE, Silvestri J, Ward SD, Corwin M, Tinsley L, Peucker M; CHIME Study Group. Crowell DH, et al. J Clin Neurophysiol. 2002 Oct;19(5):469-83. doi: 10.1097/00004691-200210000-00010. J Clin Neurophysiol. 2002. PMID: 12477992

7

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.

Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML. Weese-Mayer DE, et al. Am J Med Genet A. 2003 Mar 15;117A(3):268-74. doi: 10.1002/ajmg.a.20005. Am J Med Genet A. 2003. PMID: 12599191

8

Nighttime child care: inadequate sudden infant death syndrome risk factor knowledge, practice, and policies.

Moon RY, Weese-Mayer DE, Silvestri JM. Moon RY, et al. Pediatrics. 2003 Apr;111(4 Pt 1):795-9. doi: 10.1542/peds.111.4.795. Pediatrics. 2003. PMID: 12671114

9

Effect of a sudden infant death syndrome risk reduction education program on risk factor compliance and information sources in primarily black urban communities.

Rasinski KA, Kuby A, Bzdusek SA, Silvestri JM, Weese-Mayer DE. Rasinski KA, et al. Pediatrics. 2003 Apr;111(4 Pt 1):e347-54. doi: 10.1542/peds.111.4.e347. Pediatrics. 2003. PMID: 12671150

10

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.

Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML. Weese-Mayer DE, et al. Am J Med Genet A. 2003 Oct 15;122A(3):238-45. doi: 10.1002/ajmg.a.20427. Am J Med Genet A. 2003. PMID: 12966525

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