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Bottlenecks and beyond: mitochondrial DNA segregation in health and disease.
Brown GK. Brown GK. J Inherit Metab Dis. 1997 Mar;20(1):2-8. doi: 10.1023/a:1005336903888. J Inherit Metab Dis. 1997. PMID: 9061561 Review. No abstract available.
Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patients.
Matthews PM, Brown RM, Otero LJ, Marchington DR, LeGris M, Howes R, Meadows LS, Shevell M, Scriver CR, Brown GK. Matthews PM, et al. Brain. 1994 Jun;117 ( Pt 3):435-43. doi: 10.1093/brain/117.3.435. Brain. 1994. PMID: 8032855
Prenatal diagnosis of pyruvate dehydrogenase E1 alpha subunit deficiency.
Brown RM, Brown GK. Brown RM, et al. Prenat Diagn. 1994 Jun;14(6):435-41. doi: 10.1002/pd.1970140604. Prenat Diagn. 1994. PMID: 7937579
Atypical pyroglutamic aciduria: possible role of paracetamol.
Pitt JJ, Brown GK, Clift V, Christodoulou J. Pitt JJ, et al. J Inherit Metab Dis. 1990;13(5):755-6. doi: 10.1007/BF01799581. J Inherit Metab Dis. 1990. PMID: 2246862 No abstract available.
Pyruvate dehydrogenase E1 alpha deficiency.
Brown GK. Brown GK. J Inherit Metab Dis. 1992;15(4):625-33. doi: 10.1007/BF01799619. J Inherit Metab Dis. 1992. PMID: 1528021 Review.
A national perspective on prenatal testing for mitochondrial disease.
Nesbitt V, Alston CL, Blakely EL, Fratter C, Feeney CL, Poulton J, Brown GK, Turnbull DM, Taylor RW, McFarland R. Nesbitt V, et al. Eur J Hum Genet. 2014 Nov;22(11):1255-9. doi: 10.1038/ejhg.2014.35. Epub 2014 Mar 19. Eur J Hum Genet. 2014. PMID: 24642831 Free PMC article.
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