Fouad GT - Search Results

1

Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita.

Zhang J, George AL Jr, Griggs RC, Fouad GT, Roberts J, Kwieciński H, Connolly AM, Ptácek LJ. Zhang J, et al. Among authors: fouad gt. Neurology. 1996 Oct;47(4):993-8. doi: 10.1212/wnl.47.4.993. Neurology. 1996. PMID: 8857733

2

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.

Ptácek LJ, Tawil R, Griggs RC, Engel AG, Layzer RB, Kwieciński H, McManis PG, Santiago L, Moore M, Fouad G, et al. Ptácek LJ, et al. Cell. 1994 Jun 17;77(6):863-8. doi: 10.1016/0092-8674(94)90135-x. Cell. 1994. PMID: 8004673

3

A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q.

Fouad GT, Servidei S, Durcan S, Bertini E, Ptácek LJ. Fouad GT, et al. Am J Hum Genet. 1996 Jul;59(1):135-9. Am J Hum Genet. 1996. PMID: 8659517 Free PMC article.

4

Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis.

Fouad G, Dalakas M, Servidei S, Mendell JR, Van den Bergh P, Angelini C, Alderson K, Griggs RC, Tawil R, Gregg R, Hogan K, Powers PA, Weinberg N, Malonee W, Ptácek LJ. Fouad G, et al. Neuromuscul Disord. 1997 Jan;7(1):33-8. doi: 10.1016/s0960-8966(96)00401-4. Neuromuscul Disord. 1997. PMID: 9132138 Free article.

5

Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects.

Redig JK, Fouad GT, Babcock D, Reshey B, Feingold E, Reeves RH, Maslen CL. Redig JK, et al. Among authors: fouad gt. AIMS Genet. 2014;1(1):1-19. doi: 10.3934/genet.2014.1.1#sthash.jksuJTeC.dpuf. AIMS Genet. 2014. PMID: 25328912 Free PMC article.

6

A randomized, double-blind clinical study on the safety and tolerability of an iron multi-amino acid chelate preparation in premenopausal women.

Fouad GT, Evans M, Sharma P, Baisley J, Crowley D, Guthrie N. Fouad GT, et al. J Diet Suppl. 2013 Mar;10(1):17-28. doi: 10.3109/19390211.2012.758217. Epub 2013 Feb 7. J Diet Suppl. 2013. PMID: 23387416 Clinical Trial.

7

Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins.

Rupp PA, Fouad GT, Egelston CA, Reifsteck CA, Olson SB, Knosp WM, Glanville RW, Thornburg KL, Robinson SW, Maslen CL. Rupp PA, et al. Among authors: fouad gt. Gene. 2002 Jun 26;293(1-2):47-57. doi: 10.1016/s0378-1119(02)00696-0. Gene. 2002. PMID: 12137942

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