Barshop BA - Search Results

1

Chronic treatment of mitochondrial disease patients with dichloroacetate.

Barshop BA, Naviaux RK, McGowan KA, Levine F, Nyhan WL, Loupis-Geller A, Haas RH. Barshop BA, et al. Mol Genet Metab. 2004 Sep-Oct;83(1-2):138-49. doi: 10.1016/j.ymgme.2004.06.009. Mol Genet Metab. 2004. PMID: 15464428 Clinical Trial.

2

Transcobalamin II deficiency presenting with methylmalonic aciduria and homocystinuria and abnormal absorption of cobalamin.

Barshop BA, Wolff J, Nyhan WL, Yu A, Prodanos C, Jones G, Sweetman L, Leslie J, Holm J, Green R, et al. Barshop BA, et al. Am J Med Genet. 1990 Feb;35(2):222-8. doi: 10.1002/ajmg.1320350216. Am J Med Genet. 1990. PMID: 2309761

3

Excretion of hippuric acid during sodium benzoate therapy in patients with hyperglycinaemia or hyperammonaemia.

Barshop BA, Breuer J, Holm J, Leslie J, Nyhan WL. Barshop BA, et al. J Inherit Metab Dis. 1989;12(1):72-9. doi: 10.1007/BF01805533. J Inherit Metab Dis. 1989. PMID: 2501586

4

Duplication of 16q and deletion of 15q.

Nyhan WL, Mascarello J, Barshop B, Doroski D, Hirschhorn K. Nyhan WL, et al. Am J Med Genet. 1989 Oct;34(2):183-6. doi: 10.1002/ajmg.1320340210. Am J Med Genet. 1989. PMID: 2816995

5

Oxidative metabolism in Rett syndrome: 1. Clinical studies.

Haas RH, Light M, Rice M, Barshop BA. Haas RH, et al. Among authors: barshop ba. Neuropediatrics. 1995 Apr;26(2):90-4. doi: 10.1055/s-2007-979734. Neuropediatrics. 1995. PMID: 7566464

6

Treatment of Lesch-Nyhan syndrome with AICAR.

Page T, Barshop B, Yu AL, Nyhan WL. Page T, et al. Adv Exp Med Biol. 1994;370:353-6. doi: 10.1007/978-1-4615-2584-4_76. Adv Exp Med Biol. 1994. PMID: 7660927 No abstract available.

7

Anabolic effect of human growth hormone: management of inherited disorders of catabolic pathways.

Marsden D, Barshop BA, Capistrano-Estrada S, Rice M, Prodanos C, Sartoris D, Wolff J, Jones KL, Spector S, Nyhan WL. Marsden D, et al. Among authors: barshop ba. Biochem Med Metab Biol. 1994 Aug;52(2):145-54. doi: 10.1006/bmmb.1994.1047. Biochem Med Metab Biol. 1994. PMID: 7993663

8

Diet change in the management of metabolic encephalomyopathies.

Haas RH, Barshop BA. Haas RH, et al. Among authors: barshop ba. Biofactors. 1998;7(3):259-62. doi: 10.1002/biof.5520070323. Biofactors. 1998. PMID: 9568263 No abstract available.

9

Treatment of the acute crisis in maple syrup urine disease.

Nyhan WL, Rice-Kelts M, Klein J, Barshop BA. Nyhan WL, et al. Among authors: barshop ba. Arch Pediatr Adolesc Med. 1998 Jun;152(6):593-8. doi: 10.1001/archpedi.152.6.593. Arch Pediatr Adolesc Med. 1998. PMID: 9641714

10

Mitochondrial DNA polymerase gamma deficiency and mtDNA depletion in a child with Alpers' syndrome.

Naviaux RK, Nyhan WL, Barshop BA, Poulton J, Markusic D, Karpinski NC, Haas RH. Naviaux RK, et al. Among authors: barshop ba. Ann Neurol. 1999 Jan;45(1):54-8. doi: 10.1002/1531-8249(199901)45:1<54::aid-art10>3.0.co;2-b. Ann Neurol. 1999. PMID: 9894877

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