Rand CM - 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

Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology.

Todd ES, Weinberg SM, Berry-Kravis EM, Silvestri JM, Kenny AS, Rand CM, Zhou L, Maher BS, Marazita ML, Weese-Mayer DE. Todd ES, et al. Among authors: rand cm. Pediatr Res. 2006 Jan;59(1):39-45. doi: 10.1203/01.pdr.0000191814.73340.1d. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16327002

3

3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis.

Maher BS, Marazita ML, Rand C, Zhou L, Berry-Kravis EM, Weese-Mayer DE. Maher BS, et al. Am J Med Genet A. 2006 Jul 1;140(13):1453-7. doi: 10.1002/ajmg.a.31261. Am J Med Genet A. 2006. PMID: 16691588 No abstract available.

4

Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome.

Rand CM, Weese-Mayer DE, Maher BS, Zhou L, Marazita ML, Berry-Kravis EM. Rand CM, et al. Am J Med Genet A. 2006 Jul 1;140(13):1447-52. doi: 10.1002/ajmg.a.31306. Am J Med Genet A. 2006. PMID: 16763966

5

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.

Rand CM, Weese-Mayer DE, Zhou L, Maher BS, Cooper ME, Marazita ML, Berry-Kravis EM. Rand CM, et al. Am J Med Genet A. 2006 Aug 1;140(15):1687-91. doi: 10.1002/ajmg.a.31336. Am J Med Genet A. 2006. PMID: 16830328 No abstract available.

6

Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype.

Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer DE. Berry-Kravis EM, et al. Among authors: rand cm. Am J Respir Crit Care Med. 2006 Nov 15;174(10):1139-44. doi: 10.1164/rccm.200602-305OC. Epub 2006 Aug 3. Am J Respir Crit Care Med. 2006. PMID: 16888290

7

Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.

Rand CM, Berry-Kravis EM, Zhou L, Fan W, Weese-Mayer DE. Rand CM, et al. Pediatr Res. 2007 Aug;62(2):180-2. doi: 10.1203/PDR.0b013e3180a725a0. Pediatr Res. 2007. PMID: 17597646

8

Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood.

Ize-Ludlow D, Gray JA, Sperling MA, Berry-Kravis EM, Milunsky JM, Farooqi IS, Rand CM, Weese-Mayer DE. Ize-Ludlow D, et al. Among authors: rand cm. Pediatrics. 2007 Jul;120(1):e179-88. doi: 10.1542/peds.2006-3324. Pediatrics. 2007. PMID: 17606542

9

Genetic variation in the HTR1A gene and sudden infant death syndrome.

Morley ME, Rand CM, Berry-Kravis EM, Zhou L, Fan W, Weese-Mayer DE. Morley ME, et al. Among authors: rand cm. Am J Med Genet A. 2008 Apr 1;146A(7):930-3. doi: 10.1002/ajmg.a.32112. Am J Med Genet A. 2008. PMID: 18286597 No abstract available.

10

Congenital central hypoventilation syndrome (CCHS) and sudden infant death syndrome (SIDS): kindred disorders of autonomic regulation.

Weese-Mayer DE, Berry-Kravis EM, Ceccherini I, Rand CM. Weese-Mayer DE, et al. Among authors: rand cm. Respir Physiol Neurobiol. 2008 Dec 10;164(1-2):38-48. doi: 10.1016/j.resp.2008.05.011. Respir Physiol Neurobiol. 2008. PMID: 18579454 Review.

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