G N THOMPSON
Overview
Explore the profile of G N THOMPSON including associated specialties, affiliations and a list of published articles.
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Articles
87
Citations
436
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Recent Articles
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THOMPSON G, FRIEDMAN S
Bull Los Angel Neuro Soc
. 2010 Mar;
11(3-4):172-7.
PMID: 20285704
No abstract available.
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ROSANOFF W, THOMPSON G
Ann West Med Surg
. 2010 Mar;
1(10):411-5.
PMID: 20272387
No abstract available.
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Bouchard L, Robert M, Vinarov D, Stanley C, THOMPSON G, Morris A, et al.
Pediatr Res
. 2001 Mar;
49(3):326-31.
PMID: 11228257
Hereditary deficiency of mitochondrial HMG-CoA synthase (mHS, OMIM 600234) is a poorly defined, treatable, probably underdiagnosed condition that can cause episodes of severe hypoketotic hypoglycemia. We present clinical follow-up and...
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THOMPSON G, Hsu B, Pitt J, Treacy E, Stanley C
N Engl J Med
. 1997 Oct;
337(17):1203-7.
PMID: 9337379
No abstract available.
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Treacy E, Pitt J, Seller K, THOMPSON G, Ramus S, Cotton R
J Inherit Metab Dis
. 1996 Jan;
19(5):595-602.
PMID: 8892014
Mutation at the phenylalanine hydroxylase (PAH) locus is a cause of hyperphenylalaninaemia. Genotype-phenotype correlation relative to the predicted PAH activity may differ at the metabolite level and at the IQ...
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Michaud J, THOMPSON G, Brody L, Steel G, Obie C, Fontaine G, et al.
Am J Hum Genet
. 1995 Mar;
56(3):616-22.
PMID: 7887415
We discovered the missense mutation, A226V, in the ornithine-delta-aminotransferase (OAT) genes of two unrelated patients with gyrate atrophy of the choroid and retina (GA). One patient, who was a compound...