Rand CM - Search Results

1

Computer-aided diagnostic screen for Congenital Central Hypoventilation Syndrome with facial phenotype.

Slattery SM, Wilkinson J, Mittal A, Zheng C, Easton N, Singh S, Baker JJ, Rand CM, Khaytin I, Stewart TM, Demeter D, Weese-Mayer DE. Slattery SM, et al. Among authors: rand cm. Pediatr Res. 2024 Jun;95(7):1843-1850. doi: 10.1038/s41390-023-02990-8. Epub 2024 Jan 18. Pediatr Res. 2024. PMID: 38238566

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

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

4

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.

5

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

6

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

7

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

8

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.

9

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.

10

HTR2A variation and sudden infant death syndrome: a case-control analysis.

Rand CM, Berry-Kravis EM, Fan W, Weese-Mayer DE. Rand CM, et al. Acta Paediatr. 2009 Jan;98(1):58-61. doi: 10.1111/j.1651-2227.2008.01018.x. Epub 2008 Sep 2. Acta Paediatr. 2009. PMID: 18771483

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