Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 22

1.

Congenital central hypoventilation syndrome: inheritance and relation to sudden infant death syndrome.

Weese-Mayer DE, Silvestri JM, Marazita ML, Hoo JJ.

Am J Med Genet. 1993 Sep 1;47(3):360-7. Review.

PMID:
8135282
2.

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.

Respir Physiol Neurobiol. 2008 Dec 10;164(1-2):38-48. doi: 10.1016/j.resp.2008.05.011. Review.

PMID:
18579454
3.

Congenital central hypoventilation syndrome and sudden infant death syndrome: disorders of autonomic regulation.

Rand CM, Patwari PP, Carroll MS, Weese-Mayer DE.

Semin Pediatr Neurol. 2013 Mar;20(1):44-55. doi: 10.1016/j.spen.2013.01.005. Review.

PMID:
23465774
4.

The triple risk hypotheses in sudden infant death syndrome.

Guntheroth WG, Spiers PS.

Pediatrics. 2002 Nov;110(5):e64. Review.

PMID:
12415070
5.

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

Weese-Mayer DE, Berry-Kravis EM, Marazita ML.

Respir Physiol Neurobiol. 2005 Nov 15;149(1-3):73-82. Epub 2005 Jul 28. Review.

PMID:
16054879
6.

Congenital central hypoventilation syndrome and Hirschsprung's disease.

Croaker GD, Shi E, Simpson E, Cartmill T, Cass DT.

Arch Dis Child. 1998 Apr;78(4):316-22. Review.

7.

[Sudden infant death syndrome (SIDS)].

Guffanti S, Grancini F, Scalfaro C, Podestà AF.

Pediatr Med Chir. 2004 Mar-Apr;26(2):96-104. Review. Italian.

PMID:
15700732
8.

Sudden Infant Death Syndrome: review of implicated genetic factors.

Weese-Mayer DE, Ackerman MJ, Marazita ML, Berry-Kravis EM.

Am J Med Genet A. 2007 Apr 15;143A(8):771-88. Review.

PMID:
17340630
9.

Congenital central hypoventilation syndrome and Hirschsprung's disease in half sibs.

Hamilton J, Bodurtha JN.

J Med Genet. 1989 Apr;26(4):272-4. Review.

10.
11.

Congenital hypoventilation syndromes.

Lesser DJ, Ward SL, Kun SS, Keens TG.

Semin Respir Crit Care Med. 2009 Jun;30(3):339-47. doi: 10.1055/s-0029-1222448. Epub 2009 May 18. Review.

PMID:
19452394
12.

How common is repeat sudden infant death syndrome?

Bacon CJ, Hall DB, Stephenson TJ, Campbell MJ.

Arch Dis Child. 2008 Apr;93(4):323-6. Epub 2007 Jun 12. Review.

PMID:
17566052
13.

Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.

Weese-Mayer DE, Rand CM, Berry-Kravis EM, Jennings LJ, Loghmanee DA, Patwari PP, Ceccherini I.

Pediatr Pulmonol. 2009 Jun;44(6):521-35. doi: 10.1002/ppul.21045. Review.

PMID:
19422034
14.

[Sleep disorders in the newborn].

Alfonso I, Luzondo R, Papazian O.

Medicina (B Aires). 2007;67(6 Pt 1):556-60. Review. Spanish.

PMID:
18422081
15.

Genetics and early disturbances of breathing control.

Gaultier C, Amiel J, Dauger S, Trang H, Lyonnet S, Gallego J, Simonneau M.

Pediatr Res. 2004 May;55(5):729-33. Epub 2004 Jan 22. Review.

PMID:
14739359
16.

The role of infection in sudden infant death syndrome.

Blackwell CC, Weir DM.

FEMS Immunol Med Microbiol. 1999 Aug 1;25(1-2):1-6. Review.

17.

Ethnicity, infection and sudden infant death syndrome.

Blackwell CC, Moscovis SM, Gordon AE, Al Madani OM, Hall ST, Gleeson M, Scott RJ, Roberts-Thomson J, Weir DM, Busuttil A.

FEMS Immunol Med Microbiol. 2004 Sep 1;42(1):53-65. Review.

18.

Central congenital hypoventilation syndrome: changing face of a less mysterious but more complex genetic disorder.

Grigg-Damberger M, Wells A.

Semin Respir Crit Care Med. 2009 Jun;30(3):262-74. doi: 10.1055/s-0029-1222440. Epub 2009 May 18. Review.

PMID:
19452387
19.

Mechanisms of pathogenesis in the Sudden Infant Death Syndrome.

Leiter JC, Böhm I.

Respir Physiol Neurobiol. 2007 Nov 15;159(2):127-38. Epub 2007 Jun 8. Review.

PMID:
17644048
20.

Familial diaphragmatic defects: early prenatal diagnosis and evidence for major gene inheritance.

Bocian M, Spence MA, Marazita ML, Walker AP, Weissberg DL.

Am J Med Genet Suppl. 1986;2:163-76. Review.

PMID:
3146286

Supplemental Content

Support Center