161 related articles for article (PubMed ID: 15654231)
1. Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele.
Sebold CD; Melvin EC; Siegel D; Mehltretter L; Enterline DS; Nye JS; Kessler J; Bassuk A; Speer MC; George TM;
Genet Med; 2005 Jan; 7(1):64-7. PubMed ID: 15654231
[TBL] [Abstract][Full Text] [Related]
2. Precurrence risk of neural tube defects in siblings of infants with lipomyelomeningocele.
Forrester MB; Merz RD
Genet Med; 2005; 7(6):457. PubMed ID: 16024981
[No Abstract] [Full Text] [Related]
3. Transgenerational Inheritance of Familial Lipomyelomeningocele.
Larrew T; Eskandari R; Holden KR; Chen A; Spellicy CJ; Jones JR; Lee JA; Lyons MJ
J Child Neurol; 2017 Dec; 32(14):1118-1122. PubMed ID: 29129155
[TBL] [Abstract][Full Text] [Related]
4. Concepts in the neurosurgical care of patients with spinal neural tube defects: An embryologic approach.
Blount JP; George TM; Koueik J; Iskandar BJ
Birth Defects Res; 2019 Nov; 111(19):1564-1576. PubMed ID: 31576681
[TBL] [Abstract][Full Text] [Related]
5. Neural tube defects--disorders of neurulation and related embryonic processes.
Copp AJ; Greene ND
Wiley Interdiscip Rev Dev Biol; 2013; 2(2):213-27. PubMed ID: 24009034
[TBL] [Abstract][Full Text] [Related]
6. Spina bifida and other neural tube defects.
Northrup H; Volcik KA
Curr Probl Pediatr; 2000; 30(10):313-32. PubMed ID: 11147289
[TBL] [Abstract][Full Text] [Related]
7. Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.
Deak KL; Siegel DG; George TM; Gregory S; Ashley-Koch A; Speer MC;
Birth Defects Res A Clin Mol Teratol; 2008 Oct; 82(10):662-9. PubMed ID: 18937341
[TBL] [Abstract][Full Text] [Related]
8. Methylome analysis for spina bifida shows
Rochtus A; Winand R; Laenen G; Vangeel E; Izzi B; Wittevrongel C; Moreau Y; Verpoorten C; Jansen K; Van Geet C; Freson K
Clin Epigenetics; 2016; 8():108. PubMed ID: 27757173
[TBL] [Abstract][Full Text] [Related]
9. A novel mutation in the gene encoding noggin is not causative in human neural tube defects.
Bauer KA; George TM; Enterline DS; Stottmann RW; Melvin EC; Siegel D; Samal S; Hauser MA; Klingensmith J; Nye JS; Speer MC;
J Neurogenet; 2002; 16(1):65-71. PubMed ID: 12420790
[TBL] [Abstract][Full Text] [Related]
10. Empiric recurrence risk for neural tube defects (NTD) in Krakow region.
Pietrzyk JJ
Acta Anthropogenet; 1983; 7(4):367-72. PubMed ID: 6680315
[TBL] [Abstract][Full Text] [Related]
11. Multisite neural tube closure in humans.
Van Allen MI
Birth Defects Orig Artic Ser; 1996; 30(1):203-25. PubMed ID: 9125329
[TBL] [Abstract][Full Text] [Related]
12. Interaction between maternal periconceptional supplementation of folic acid and reduced folate carrier gene polymorphism of neural tube defects.
Pei LJ; Zhu HP; Li ZW; Zhang W; Ren AG; Zhu JH; Li Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):284-7. PubMed ID: 15952116
[TBL] [Abstract][Full Text] [Related]
13. Association of main folate metabolic pathway gene polymorphisms with neural tube defects in Han population of Northern China.
Fang Y; Zhang R; Zhi X; Zhao L; Cao L; Wang Y; Cai C
Childs Nerv Syst; 2018 Apr; 34(4):725-729. PubMed ID: 29392422
[TBL] [Abstract][Full Text] [Related]
14. Etiologic heterogeneity of neural tube defects. II. Clues from family studies.
Khoury MJ; Erickson JD; James LM
Am J Hum Genet; 1982 Nov; 34(6):980-7. PubMed ID: 7180852
[TBL] [Abstract][Full Text] [Related]
15. Evidence for multi-site closure of the neural tube in humans.
Van Allen MI; Kalousek DK; Chernoff GF; Juriloff D; Harris M; McGillivray BC; Yong SL; Langlois S; MacLeod PM; Chitayat D
Am J Med Genet; 1993 Oct; 47(5):723-43. PubMed ID: 8267004
[TBL] [Abstract][Full Text] [Related]
16. Association of neural tube defects with maternal alterations and genetic polymorphisms in one-carbon metabolic pathway.
Cai CQ; Fang YL; Shu JB; Zhao LS; Zhang RP; Cao LR; Wang YZ; Zhi XF; Cui HL; Shi OY; Liu W
Ital J Pediatr; 2019 Mar; 45(1):37. PubMed ID: 30867013
[TBL] [Abstract][Full Text] [Related]
17. Etiology, pathogenesis and prevention of neural tube defects.
Padmanabhan R
Congenit Anom (Kyoto); 2006 Jun; 46(2):55-67. PubMed ID: 16732763
[TBL] [Abstract][Full Text] [Related]
18. Epidemiology of neural tube defects.
Frey L; Hauser WA
Epilepsia; 2003; 44 Suppl 3():4-13. PubMed ID: 12790881
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of cystathionine beta synthase gene mutation 852Ins68 as a possible risk for neural tube defects in eastern India.
Saxena AK; Gupta J; Pandey S; Gangopadhaya AN; Pandey LK
Genet Mol Res; 2011 Oct; 10(4):2424-9. PubMed ID: 22002135
[TBL] [Abstract][Full Text] [Related]
20. DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects.
Rochtus A; Izzi B; Vangeel E; Louwette S; Wittevrongel C; Lambrechts D; Moreau Y; Winand R; Verpoorten C; Jansen K; Van Geet C; Freson K
Epigenetics; 2015; 10(1):92-101. PubMed ID: 25565354
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
