Fowler B - Search Results

1

Hyperhomocysteinemia: an independent risk factor for vascular disease.

Clarke R, Daly L, Robinson K, Naughten E, Cahalane S, Fowler B, Graham I. Clarke R, et al. Among authors: fowler b. N Engl J Med. 1991 Apr 25;324(17):1149-55. doi: 10.1056/NEJM199104253241701. N Engl J Med. 1991. PMID: 2011158

2

Hyperhomocysteinemia in premature arterial disease: examination of cystathionine beta-synthase alleles at the molecular level.

Kozich V, Kraus E, de Franchis R, Fowler B, Boers GH, Graham I, Kraus JP. Kozich V, et al. Among authors: fowler b. Hum Mol Genet. 1995 Apr;4(4):623-9. doi: 10.1093/hmg/4.4.623. Hum Mol Genet. 1995. PMID: 7633411

3

Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease.

Boers GH, Smals AG, Trijbels FJ, Fowler B, Bakkeren JA, Schoonderwaldt HC, Kleijer WJ, Kloppenborg PW. Boers GH, et al. Among authors: fowler b. N Engl J Med. 1985 Sep 19;313(12):709-15. doi: 10.1056/NEJM198509193131201. N Engl J Med. 1985. PMID: 4033695

4

Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosis.

Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, Fowler B, Seligsohn U. Mandel H, et al. Among authors: fowler b. N Engl J Med. 1996 Mar 21;334(12):763-8. doi: 10.1056/NEJM199603213341204. N Engl J Med. 1996. PMID: 8592550

5

Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.

Boers GH, Fowler B, Smals AG, Trijbels FJ, Leermakers AI, Kleijer WJ, Kloppenborg PW. Boers GH, et al. Among authors: fowler b. Hum Genet. 1985;69(2):164-9. doi: 10.1007/BF00293290. Hum Genet. 1985. PMID: 3972418

6

Homocysteine: overview of biochemistry, molecular biology, and role in disease processes.

Fowler B. Fowler B. Semin Vasc Med. 2005 May;5(2):77-86. doi: 10.1055/s-2005-872394. Semin Vasc Med. 2005. PMID: 16047261 Review.

7

An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1.

Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR 2nd, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, Rosenblatt DS, Venditti CP, Shaikh TH. Yu HC, et al. Among authors: fowler b. Am J Hum Genet. 2013 Sep 5;93(3):506-14. doi: 10.1016/j.ajhg.2013.07.022. Am J Hum Genet. 2013. PMID: 24011988 Free PMC article.

8

[Homocystinuria].

Houst'ková H, Zeman J, Hyánek J, Fowler B, Mandys V, Simková M. Houst'ková H, et al. Among authors: fowler b. Cesk Pediatr. 1985 Jul;40(7):389-91. Cesk Pediatr. 1985. PMID: 4028241 Czech. No abstract available.

9

Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism.

Stucki M, Coelho D, Suormala T, Burda P, Fowler B, Baumgartner MR. Stucki M, et al. Among authors: fowler b. Hum Mol Genet. 2012 Mar 15;21(6):1410-8. doi: 10.1093/hmg/ddr579. Epub 2011 Dec 8. Hum Mol Genet. 2012. PMID: 22156578

10

Isolated 3-methylcrotonyl-CoA carboxylase deficiency: evidence for an allele-specific dominant negative effect and responsiveness to biotin therapy.

Baumgartner MR, Dantas MF, Suormala T, Almashanu S, Giunta C, Friebel D, Gebhardt B, Fowler B, Hoffmann GF, Baumgartner ER, Valle D. Baumgartner MR, et al. Among authors: fowler b. Am J Hum Genet. 2004 Nov;75(5):790-800. doi: 10.1086/425181. Epub 2004 Sep 9. Am J Hum Genet. 2004. PMID: 15359379 Free PMC article.

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