Northrup H - Search Results

1

Spina bifida and other neural tube defects.

Northrup H, Volcik KA. Northrup H, et al. Curr Probl Pediatr. 2000 Nov-Dec;30(10):313-32. doi: 10.1067/mpp.2000.112052. Curr Probl Pediatr. 2000. PMID: 11147289 Review.

2

Germ-line mutational analysis of the TSC2 gene in 90 tuberous-sclerosis patients.

Au KS, Rodriguez JA, Finch JL, Volcik KA, Roach ES, Delgado MR, Rodriguez E Jr, Northrup H. Au KS, et al. Among authors: northrup h. Am J Hum Genet. 1998 Feb;62(2):286-94. doi: 10.1086/301705. Am J Hum Genet. 1998. PMID: 9463313 Free PMC article.

3

Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics.

Volcik KA, Blanton SH, Tyerman GH, Jong ST, Rott EJ, Page TZ, Romaine NK, Northrup H. Volcik KA, et al. Among authors: northrup h. Am J Med Genet. 2000 Nov 6;95(1):21-7. Am J Med Genet. 2000. PMID: 11074490

4

Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability.

Volcik KA, Blanton SH, Northrup H. Volcik KA, et al. Among authors: northrup h. Am J Hum Genet. 2001 Nov;69(5):1150-3. doi: 10.1086/324066. Am J Hum Genet. 2001. PMID: 11590551 Free PMC article. No abstract available.

5

Testing for genetic associations with the PAX gene family in a spina bifida population.

Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H. Volcik KA, et al. Among authors: northrup h. Am J Med Genet. 2002 Jul 1;110(3):195-202. doi: 10.1002/ajmg.10434. Am J Med Genet. 2002. PMID: 12116225

6

Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects.

Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H. Volcik KA, et al. Among authors: northrup h. Am J Med Genet. 2002 Jul 1;110(3):203-7. doi: 10.1002/ajmg.10435. Am J Med Genet. 2002. PMID: 12116226

7

Spinal lesion level in spina bifida: a source of neural and cognitive heterogeneity.

Fletcher JM, Copeland K, Frederick JA, Blaser SE, Kramer LA, Northrup H, Hannay HJ, Brandt ME, Francis DJ, Villarreal G, Drake JM, Laurent JP, Townsend I, Inwood S, Boudousquie A, Dennis M. Fletcher JM, et al. Among authors: northrup h. J Neurosurg. 2005 Apr;102(3 Suppl):268-79. doi: 10.3171/ped.2005.102.3.0268. J Neurosurg. 2005. PMID: 15881750

8

Promotor genotype of the platelet-derived growth factor receptor-alpha gene shows population stratification but not association with spina bifida meningomyelocele.

Au KS, Northrup H, Kirkpatrick TJ, Volcik KA, Fletcher JM, Townsend IT, Blanton SH, Tyerman GH, Villarreal G, King TM. Au KS, et al. Among authors: northrup h. Am J Med Genet A. 2005 Dec 15;139(3):194-8. doi: 10.1002/ajmg.a.31002. Am J Med Genet A. 2005. PMID: 16283668 Free PMC article.

9

Genes in glucose metabolism and association with spina bifida.

Davidson CM, Northrup H, King TM, Fletcher JM, Townsend I, Tyerman GH, Au KS. Davidson CM, et al. Among authors: northrup h. Reprod Sci. 2008 Jan;15(1):51-8. doi: 10.1177/1933719107309590. Reprod Sci. 2008. PMID: 18212354 Free PMC article.

10

Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals.

Au KS, Tran PX, Tsai CC, O'Byrne MR, Lin JI, Morrison AC, Hampson AW, Cirino P, Fletcher JM, Ostermaier KK, Tyerman GH, Doebel S, Northrup H. Au KS, et al. Among authors: northrup h. Birth Defects Res A Clin Mol Teratol. 2008 Oct;82(10):692-700. doi: 10.1002/bdra.20499. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18937358 Free PMC article.

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