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3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children.
Gibson KM, Bennett MJ, Naylor EW, Morton DH. Gibson KM, et al. J Pediatr. 1998 Mar;132(3 Pt 1):519-23. doi: 10.1016/s0022-3476(98)70032-0. J Pediatr. 1998. PMID: 9544913
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects.
Gibson KM, Bennett MJ, Mize CE, Jakobs C, Rotig A, Munnich A, Lichter-Konecki U, Trefz FK. Gibson KM, et al. J Pediatr. 1992 Dec;121(6):940-2. doi: 10.1016/s0022-3476(05)80348-8. J Pediatr. 1992. PMID: 1447663
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.
Gibson KM, Lee CF, Wappner RS. Gibson KM, et al. J Inherit Metab Dis. 1992;15(3):363-6. doi: 10.1007/BF02435977. J Inherit Metab Dis. 1992. PMID: 1383605 No abstract available.
Further evaluation of Vigabatrin therapy in 4-hydroxybutyric aciduria.
Jakobs C, Michael T, Jaeger E, Jaeken J, Gibson KM. Jakobs C, et al. Among authors: gibson km. Eur J Pediatr. 1992 Jun;151(6):466. doi: 10.1007/BF01959366. Eur J Pediatr. 1992. PMID: 1628679 No abstract available.
Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria.
Gibson KM, Sherwood WG, Hoffman GF, Stumpf DA, Dianzani I, Schutgens RB, Barth PG, Weismann U, Bachmann C, Schrynemackers-Pitance P, et al. Gibson KM, et al. J Pediatr. 1991 Jun;118(6):885-90. doi: 10.1016/s0022-3476(05)82199-7. J Pediatr. 1991. PMID: 1710267
Succinic semialdehyde dehydrogenase deficiency associated with combined 4-hydroxybutyric and dicarboxylic acidurias: potential for clinical misdiagnosis based on urinary organic acid profiling.
Gibson KM, Goodman SI, Frerman FE, Glasgow AM. Gibson KM, et al. J Pediatr. 1989 Apr;114(4 Pt 1):607-10. doi: 10.1016/s0022-3476(89)80706-1. J Pediatr. 1989. PMID: 2926573 No abstract available.
Clinical and biochemical phenotype in 11 patients with mevalonic aciduria.
Hoffmann GF, Charpentier C, Mayatepek E, Mancini J, Leichsenring M, Gibson KM, Divry P, Hrebicek M, Lehnert W, Sartor K, et al. Hoffmann GF, et al. Among authors: gibson km. Pediatrics. 1993 May;91(5):915-21. Pediatrics. 1993. PMID: 8386351
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.
Ibel H, Endres W, Hadorn HB, Deufel T, Paetzke I, Duran M, Kennaway NG, Gibson KM. Ibel H, et al. Among authors: gibson km. Eur J Pediatr. 1993 Aug;152(8):665-70. doi: 10.1007/BF01955244. Eur J Pediatr. 1993. PMID: 7691603
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts.
Burlina AB, Dionisi-Vici C, Bennett MJ, Gibson KM, Servidei S, Bertini E, Hale DE, Schmidt-Sommerfeld E, Sabetta G, Zacchello F, et al. Burlina AB, et al. Among authors: gibson km. J Pediatr. 1994 Jan;124(1):79-86. doi: 10.1016/s0022-3476(94)70257-8. J Pediatr. 1994. PMID: 8283379
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