Weese-Mayer DE - Search Results

1

Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation: analysis of hypothalamic and autonomic candidate genes.

Rand CM, Patwari PP, Rodikova EA, Zhou L, Berry-Kravis EM, Wilson RJ, Bech-Hansen T, Weese-Mayer DE. Rand CM, et al. Pediatr Res. 2011 Oct;70(4):375-8. doi: 10.1203/PDR.0b013e318229474d. Pediatr Res. 2011. PMID: 21691246

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

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

4

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

5

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

6

Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.

Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Silvestri JM, Curran ME, Marazita ML. Weese-Mayer DE, et al. Am J Med Genet A. 2003 Dec 15;123A(3):267-78. doi: 10.1002/ajmg.a.20527. Am J Med Genet A. 2003. PMID: 14608649

7

Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan disease.

Weese-Mayer DE, Berry-Kravis EM. Weese-Mayer DE, et al. Am J Respir Crit Care Med. 2004 Jul 1;170(1):16-21. doi: 10.1164/rccm.200402-245PP. Epub 2004 Apr 22. Am J Respir Crit Care Med. 2004. PMID: 15105164 Review. No abstract available.

8

Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.

Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Curran ME, Silvestri JM, Marazita ML. Weese-Mayer DE, et al. Pediatr Res. 2004 Sep;56(3):391-5. doi: 10.1203/01.PDR.0000136285.91048.4A. Epub 2004 Jul 7. Pediatr Res. 2004. PMID: 15240857

9

Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.

Weese-Mayer DE, Berry-Kravis EM, Zhou L. Weese-Mayer DE, et al. Am J Respir Crit Care Med. 2005 Jan 1;171(1):88. doi: 10.1164/ajrccm.171.1.950. Am J Respir Crit Care Med. 2005. PMID: 15615891 No abstract available.

10

In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome.

Weese-Mayer DE, Berry-Kravis EM, Marazita ML. Weese-Mayer DE, et al. Respir Physiol Neurobiol. 2005 Nov 15;149(1-3):73-82. doi: 10.1016/j.resp.2005.06.010. Epub 2005 Jul 28. Respir Physiol Neurobiol. 2005. PMID: 16054879 Review.

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