Author:
Bertini E.,Dionisi-Vici C.,Garavaglia B.,Burlina A. B.,Sabatelli M.,Rimoldi M.,Bartuli A.,Sabetta G.,DiDonato S.
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference22 articles.
1. Burlina AB (1986) The role of urinary organic acids analysis in the detection and management of inherited metabolic diseases. Ital J Pediatr 12:541–551
2. Deckar K, Crotomny P (1974) Coenzyme A. In: Bergmeyer (ed) Methods of enzymatic analysis, vol 4. Academic Press, New York, pp 2017–2021
3. DiDonato S, Garavaglia B, Strisciuglio P, Borrone C, Andria G (1988) Multisystem triglyceride storage disease is due to a specific defect in the degradation of endocellularly synthesized triglycerides. Neurology 38:1107–1110
4. DiDonato S, Gellera C, Peluchetti D, Uziel G, Antonelli A, Lus G, Rimoldi M (1989) Normalization of short-chain acylcoenzyme A dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme A dehydrogenase-deficient myopathy. Ann Neurol 25:479–484
5. Dubowitz V (1985) Muscle biopsy. A practical approach. Bailleiere-Tindall, London, pp 3–40
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