18Fluoro-2-deoxyglucose (18FDG) PET scan of the brain in type IV 3-methylglutaconic aciduria: clinical and MRI correlations
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P. Ozand | Z. Patay | J. Powe | S. Bakheet | M. Al-Essa | L. al-Shamsan | L. Al-Shamsan
[1] P. Ozand,et al. CT and MR of the brain in the diagnosis of organic acidemias Experiences from 107 patients , 1994, Brain and Development.
[2] G. Gascon,et al. 3-Methylglutaconic aciduria: ten new cases with a possible new phenotype , 1994, Brain and Development.
[3] R. Kelley. Quantification of 3-methylglutaconic acid in urine, plasma, and amniotic fluid by isotope-dilution gas chromatography/mass spectrometry. , 1993, Clinica chimica acta; international journal of clinical chemistry.
[4] K. Gibson,et al. Multiple syndromes of 3-methylglutaconic aciduria. , 1993, Pediatric neurology.
[5] N. Gadoth,et al. 3‐Methylglutaconic aciduria in “optic atrophy plus” , 1993, Annals of neurology.
[6] A. Munnich,et al. 3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects. , 1992, The Journal of pediatrics.
[7] S. Lindstedt,et al. Mitochondrial ATP-Synthase Deficiency in a Child with 3-Methylglutaconic Aciduria , 1992, Pediatric Research.
[8] O. Elpeleg,et al. Behr's syndrome and 3-methylglutaconic aciduria. , 1992, American journal of ophthalmology.
[9] O. Elpeleg,et al. 3-Methylglutaconic aciduria: a new variant. , 1992, Pediatrics.
[10] B. Clark,et al. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria. , 1991, The Journal of pediatrics.
[11] I. Dianzani,et al. Phenotypic heterogeneity in the syndromes of 3-methylglutaconic aciduria. , 1991, The Journal of pediatrics.
[12] L. Wilkins. Assessment: Positron emission tomography , 1991 .
[13] M. Durán,et al. Deficiency of 3-methylglutaconyl-coenzyme A hydratase in two siblings with 3-methylglutaconic aciduria. , 1986, The Journal of clinical investigation.
[14] H. Rudney,et al. [37] 4-Hydroxybenzoate polyprenyltransferase from rat liver , 1985 .
[15] O. Hjalmarson,et al. 3-Methylglutaconic aciduria in two infants. , 1983, Clinica chimica acta; international journal of clinical chemistry.
[16] M. Durán,et al. Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism. , 1982, The Journal of pediatrics.