Ribes A - Search Results

1

Significance of bound glutarate in the diagnosis of glutaric aciduria type I.

Ribes A, Riudor E, Briones P, Christensen E, Campistol J, Millington DS. Ribes A, et al. J Inherit Metab Dis. 1992;15(3):367-70. doi: 10.1007/BF02435978. J Inherit Metab Dis. 1992. PMID: 1405471 No abstract available.

2

Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Ribes A, Riudor E, Navarro C, Boronat M, Marti M, Hale DE. Ribes A, et al. J Inherit Metab Dis. 1992;15(2):278-9. doi: 10.1007/BF01799642. J Inherit Metab Dis. 1992. PMID: 1527994 No abstract available.

3

Glutaric aciduria type I: unusual biochemical presentation.

Campistol J, Ribes A, Alvarez L, Christensen E, Millington DS. Campistol J, et al. Among authors: ribes a. J Pediatr. 1992 Jul;121(1):83-6. doi: 10.1016/s0022-3476(05)82548-x. J Pediatr. 1992. PMID: 1625098

4

Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase.

Vilaseca MA, Briones P, Ribes A, Carreras E, Llácer A, Querol J. Vilaseca MA, et al. Among authors: ribes a. J Inherit Metab Dis. 1991;14(3):285-8. doi: 10.1007/BF01811683. J Inherit Metab Dis. 1991. PMID: 1663190 No abstract available.

5

Liver transplantation in two children with tyrosinaemia type I: biochemical aspects.

Riudor E, Ribes A, Lloret J, Friden J, Holme E, Jakobs C, Martinez Ibanez V. Riudor E, et al. Among authors: ribes a. J Inherit Metab Dis. 1991;14(3):281-4. doi: 10.1007/BF01811682. J Inherit Metab Dis. 1991. PMID: 1770775 No abstract available.

6

Sudden death in an infant with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

Ribes A, Briones P, Vilaseca MA, Baraibar R, Gairi JM. Ribes A, et al. J Inherit Metab Dis. 1990;13(5):752-3. doi: 10.1007/BF01799579. J Inherit Metab Dis. 1990. PMID: 2246860 No abstract available.

7

Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patient.

Ribes A, Briones P, Vilaseca MA, Lluch M, Rodes M, Maya A, Campistol J, Pascual P, Suormala T, Baumgartner R. Ribes A, et al. Eur J Pediatr. 1990 Mar;149(6):412-5. doi: 10.1007/BF02009662. Eur J Pediatr. 1990. PMID: 2332011

8

A new case of holocarboxylase synthetase deficiency.

Briones P, Ribes A, Vilaseca MA, Rodríguez-Valcárcel G, Thuy LP, Sweetman L. Briones P, et al. Among authors: ribes a. J Inherit Metab Dis. 1989;12(3):329-30. doi: 10.1007/BF01799228. J Inherit Metab Dis. 1989. PMID: 2515377 No abstract available.

9

Requirement of high biotin doses in a case of biotinidase deficiency.

Riudor E, Vilaseca MA, Briones P, Ribes A, Suñé J, Martorell R, Macaya A, Roig M, Ballabriga A. Riudor E, et al. Among authors: ribes a. J Inherit Metab Dis. 1989;12(3):338-9. doi: 10.1007/BF01799233. J Inherit Metab Dis. 1989. PMID: 2515382 No abstract available.

10

[Organic aciduria. Forms of presentation and treatment].

Campistol J, Ribes A. Campistol J, et al. Among authors: ribes a. An Esp Pediatr. 1986 Apr;24(4):232-40. An Esp Pediatr. 1986. PMID: 3729191 Spanish.

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