Cited by

• Metabolic pigmentary retinopathies: diagnosis and therapeutic attempts.

  Poll-The BT, Billette de Villemeur T, Abitbol M, Dufier JL, Saudubray JM. Poll-The BT, et al. Eur J Pediatr. 1992 Jan;151(1):2-11. doi: 10.1007/BF02073880. Eur J Pediatr. 1992. PMID: 1728538 Review.
• Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency.

  Bertini E, Dionisi-Vici C, Garavaglia B, Burlina AB, Sabatelli M, Rimoldi M, Bartuli A, Sabetta G, DiDonato S. Bertini E, et al. Eur J Pediatr. 1992 Feb;151(2):121-6. doi: 10.1007/BF01958956. Eur J Pediatr. 1992. PMID: 1537353
• Disorders of mitochondrial long-chain fatty acid oxidation.

  Pollitt RJ. Pollitt RJ. J Inherit Metab Dis. 1995;18(4):473-90. doi: 10.1007/BF00710058. J Inherit Metab Dis. 1995. PMID: 7494405 Review.
• 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment.

  Duran M, Wanders RJ, de Jager JP, Dorland L, Bruinvis L, Ketting D, Ijlst L, van Sprang FJ. Duran M, et al. Eur J Pediatr. 1991 Jan;150(3):190-5. doi: 10.1007/BF01963564. Eur J Pediatr. 1991. PMID: 2044590
• Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: different clinical expression in three unrelated patients.

  Wanders RJ, Ijlst L, Duran M, Jakobs C, de Klerk JB, Przyrembel H, Rocchiccioli F, Aubourg P. Wanders RJ, et al. J Inherit Metab Dis. 1991;14(3):325-8. doi: 10.1007/BF01811694. J Inherit Metab Dis. 1991. PMID: 1770784 No abstract available.