Brown GK - Search Results

1

Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: evidence of alpha-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial beta-oxidation.

Brown GK, Cromby CH, Manning NJ, Pollitt RJ. Brown GK, et al. J Inherit Metab Dis. 1987;10(4):367-75. doi: 10.1007/BF01799979. J Inherit Metab Dis. 1987. PMID: 3126356

2

Characterization of the mutations in three patients with pyruvate dehydrogenase E1 alpha deficiency.

Hansen LL, Brown GK, Kirby DM, Dahl HH. Hansen LL, et al. Among authors: brown gk. J Inherit Metab Dis. 1991;14(2):140-51. doi: 10.1007/BF01800586. J Inherit Metab Dis. 1991. PMID: 1909401

3

Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiency.

Brown GK, Scholem RD, Hunt SM, Harrison JR, Pollard AC. Brown GK, et al. J Inherit Metab Dis. 1987;10(4):359-66. doi: 10.1007/BF01799978. J Inherit Metab Dis. 1987. PMID: 3126355

4

X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation.

Dahl HH, Hansen LL, Brown RM, Danks DM, Rogers JG, Brown GK. Dahl HH, et al. Among authors: brown rm, brown gk. J Inherit Metab Dis. 1992;15(6):835-47. doi: 10.1007/BF01800219. J Inherit Metab Dis. 1992. PMID: 1293379

5

Atypical pyroglutamic aciduria: possible role of paracetamol.

Pitt JJ, Brown GK, Clift V, Christodoulou J. Pitt JJ, et al. Among authors: brown gk. J Inherit Metab Dis. 1990;13(5):755-6. doi: 10.1007/BF01799581. J Inherit Metab Dis. 1990. PMID: 2246862 No abstract available.

6

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.

7

Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene.

Dahl HH, Brown GK, Brown RM, Hansen LL, Kerr DS, Wexler ID, Patel MS, De Meirleir L, Lissens W, Chun K, et al. Dahl HH, et al. Among authors: brown rm, brown gk. Hum Mutat. 1992;1(2):97-102. doi: 10.1002/humu.1380010203. Hum Mutat. 1992. PMID: 1301207 Review.

8

Succinic semialdehyde dehydrogenase deficiency--a further case.

Haan EA, Brown GK, Mitchell D, Danks DM. Haan EA, et al. Among authors: brown gk. J Inherit Metab Dis. 1985;8(3):99. doi: 10.1007/BF01819287. J Inherit Metab Dis. 1985. PMID: 2433500 No abstract available.

9

A novel mutation (P316L) in a female with pyruvate dehydrogenase E1 alpha deficiency.

Takakubo F, Thorburn DR, Brown RM, Brown GK, Dahl HH. Takakubo F, et al. Among authors: brown rm, brown gk. Hum Mutat. 1995;6(3):274-5. doi: 10.1002/humu.1380060317. Hum Mutat. 1995. PMID: 8535453 No abstract available.

10

Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).

Hayasaka K, Brown GK, Danks DM, Droste M, Kadenbach B. Hayasaka K, et al. Among authors: brown gk. J Inherit Metab Dis. 1989;12(3):247-56. doi: 10.1007/BF01799214. J Inherit Metab Dis. 1989. PMID: 2559245

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