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X-linked recessive aqueductal stenosis without macrocephaly.
Kelley RI, Mennuti MT, Hickey WF, Zackai EH. Kelley RI, et al. Clin Genet. 1988 May;33(5):390-4. doi: 10.1111/j.1399-0004.1988.tb03467.x. Clin Genet. 1988. PMID: 3378368
Mendelian etiologies of stroke.
Natowicz M, Kelley RI. Natowicz M, et al. Ann Neurol. 1987 Aug;22(2):175-92. doi: 10.1002/ana.410220202. Ann Neurol. 1987. PMID: 3310853 Review.
"If We Don't Produce, Bring Another:" Work Organization and Tomato Worker Health.
Kelley RI, Ivey SL, Silver K, Holmes SM. Kelley RI, et al. J Agromedicine. 2020 Feb 29:1-16. doi: 10.1080/1059924X.2020.1725698. Online ahead of print. J Agromedicine. 2020. PMID: 32116142
A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome.
Wassif CA, Kratz L, Sparks SE, Wheeler C, Bianconi S, Gropman A, Calis KA, Kelley RI, Tierney E, Porter FD. Wassif CA, et al. Among authors: kelley ri. Genet Med. 2017 Mar;19(3):297-305. doi: 10.1038/gim.2016.102. Epub 2016 Aug 11. Genet Med. 2017. PMID: 27513191 Free PMC article. Clinical Trial.
Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain.
Driver AM, Kratz LE, Kelley RI, Stottmann RW. Driver AM, et al. Among authors: kelley ri. Neurobiol Dis. 2016 Jul;91:69-82. doi: 10.1016/j.nbd.2016.02.017. Epub 2016 Feb 24. Neurobiol Dis. 2016. PMID: 26921468 Free PMC article.
Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies.
Wang G, McCain ML, Yang L, He A, Pasqualini FS, Agarwal A, Yuan H, Jiang D, Zhang D, Zangi L, Geva J, Roberts AE, Ma Q, Ding J, Chen J, Wang DZ, Li K, Wang J, Wanders RJ, Kulik W, Vaz FM, Laflamme MA, Murry CE, Chien KR, Kelley RI, Church GM, Parker KK, Pu WT. Wang G, et al. Among authors: kelley ri. Nat Med. 2014 Jun;20(6):616-23. doi: 10.1038/nm.3545. Epub 2014 May 11. Nat Med. 2014. PMID: 24813252 Free PMC article.
Clinical laboratory studies in Barth Syndrome.
Vernon HJ, Sandlers Y, McClellan R, Kelley RI. Vernon HJ, et al. Among authors: kelley ri. Mol Genet Metab. 2014 Jun;112(2):143-7. doi: 10.1016/j.ymgme.2014.03.007. Epub 2014 Mar 30. Mol Genet Metab. 2014. PMID: 24751896 Clinical Trial.
Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup.
Strauss KA, DuBiner L, Simon M, Zaragoza M, Sengupta PP, Li P, Narula N, Dreike S, Platt J, Procaccio V, Ortiz-González XR, Puffenberger EG, Kelley RI, Morton DH, Narula J, Wallace DC. Strauss KA, et al. Among authors: kelley ri. Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3453-8. doi: 10.1073/pnas.1300690110. Epub 2013 Feb 11. Proc Natl Acad Sci U S A. 2013. PMID: 23401503 Free PMC article.
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