Literature DB >> 85928

beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome.

J V Leonard, J W Seakins, N K Griffin.   

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Year:  1979        PMID: 85928     DOI: 10.1016/s0140-6736(79)91137-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  14 in total

1.  The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria.

Authors:  G N Thompson; R A Chalmers; D Halliday
Journal:  Eur J Pediatr       Date:  1990-02       Impact factor: 3.183

2.  3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review.

Authors:  S J Wysocki; R Hähnel
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  3-Hydroxy-3-methylglutaryl-CoA lyase deficiency.

Authors:  J H Walter; P T Clayton; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

Review 4.  3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients.

Authors:  K M Gibson; J Breuer; W L Nyhan
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

5.  3-Hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) lyase deficiency in Saudi Arabia.

Authors:  P T Ozand; A al Aqeel; G Gascon; J Brismar; E Thomas; H Gleispach
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

6.  A child with acute pancreatitis and recurrent hypoglycemia due to 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

Authors:  W G Wilson; M B Cass; O Søvik; K M Gibson; L Sweetman
Journal:  Eur J Pediatr       Date:  1984-09       Impact factor: 3.183

7.  CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase.

Authors:  G Lisson; D Leupold; D Bechinger; C Wallesch
Journal:  Neuroradiology       Date:  1981       Impact factor: 2.804

8.  Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.

Authors:  B E Kendall; D P Kingsley; J V Leonard; S Lingam; V G Oberholzer
Journal:  J Neurol Neurosurg Psychiatry       Date:  1983-01       Impact factor: 10.154

9.  3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an infant with macrocephaly and mild metabolic acidosis.

Authors:  D Leupold; M Bojasch; C Jakobs
Journal:  Eur J Pediatr       Date:  1982-02       Impact factor: 3.183

10.  Inherited disorders of 3-methylcrotonyl CoA carboxylation.

Authors:  J V Leonard; J W Seakins; K Bartlett; J Hyde; J Wilson; B Clayton
Journal:  Arch Dis Child       Date:  1981-01       Impact factor: 3.791

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