Striking improvement of muscle strength under creatine therapy in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyKORENKE, G. C; WANDERS, R. J. A; HANEFELD, F et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 1, pp 67-68, issn 0141-8955, 2 p.Article

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency : a severe fatty acid oxidation disorderSEWELL, A. C; BENDER, S. W; WIRTH, S et al.European journal of pediatrics. 1994, Vol 153, Num 10, pp 745-750, issn 0340-6199Article

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of two new mutationsIJLST, L; OOSTHEIM, W; RUITER, J. P. N et al.Journal of inherited metabolic disease. 1997, Vol 20, Num 3, pp 420-422, issn 0141-8955Conference Paper

Geflügelfleisch: Nachweis von Gefrierverfahren = Poultry meat: determining freezing methodsNIEMANN, C; BENEKE, B; BENTLER, W et al.Fleischwirtschaft (Frankfurt). 1995, Vol 75, Num 3, pp 323-326, issn 0015-363XArticle

Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometryCARPENTER, K. H; WILCKEN, B.Journal of inherited metabolic disease. 1999, Vol 22, Num 7, pp 840-841, issn 0141-8955Article

Effect of freezing on the β-hydroxyacyl-CoA-dehydrogenase(HADH) activity of fish meatPAVLOV, A; DE FERNANDO, G. D. G; DIAZ, O et al.Zeitschrift für Lebensmittel-Untersuchung und -Forschung. 1994, Vol 198, Num 6, pp 465-468, issn 0044-3026Article

Paternal Isodisomy of Chromosome 2 as a Cause of Long Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) DeficiencyBASKIN, Berivan; GERAGHTY, Michael; RAY, Peter N et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 7, pp 1808-1811, issn 1552-4825, 4 p.Article

Néovascularisation choroïdienne au cours d'un déficit en Long-Chain 3-Hydroxyacyl CoA Dehydrogenase (LCHAD) = Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency and choroidal neovascularizationSTOPEK, D; GITTEAU LALA, E; LABARTHE, F et al.Journal français d'ophtalmologie. 2008, Vol 31, Num 10, pp 993-998, issn 0181-5512, 6 p.Article

Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutationTYNI, T; RAPOLA, J; PALOTIE, A et al.The Journal of pediatrics. 1997, Vol 131, Num 5, pp 766-768, issn 0022-3476Article

Mitochondrial fatty acid β-oxidation in the human eye and brain: Implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyTYNI, Tiina; PAETAU, Anders; STRAUSS, Arnold W et al.Pediatric research. 2004, Vol 56, Num 5, pp 744-750, issn 0031-3998, 7 p.Article

Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficienciesLUNDY, C. T; SHIELD, J. P. H; KVITTINGEN, E. A et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 6, pp 537-541, issn 0141-8955, 5 p.Article

What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?LUND, A. M; DIXON, M. A; VREKEN, P et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 4, pp 353-360, issn 0141-8955, 8 p.Article

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency : Neonatal manifestation at the first day of life presenting with tachypnoeaTHIEL, C; BAUDACH, S; SCHNACKENBERG, U et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 7, pp 839-840, issn 0141-8955Article

High aerobic capacities in the skeletal muscles of pinnipeds : adaptations to diving hypoxiaKANATOUS, S. B; DIMICHELE, L. V; COWAN, D. F et al.Journal of applied physiology (1985). 1999, Vol 86, Num 4, pp 1247-1256, issn 8750-7587Article

Use of β-hydroxyacyl-CoA-dehydrogenase (HADH) activity to differentiate frozen from unfrozen fish and shellfishFERNANDEZ, M; MANO, S; GARCIA DE FERNANDO, G. D et al.Zeitschrift fur Lebensmittel-Untersuchung und -Forschung. A, European food research and technology (Print). 1999, Vol 209, Num 3-4, pp 205-208, issn 1431-4630Article

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation : Clinical presentation of thirteen patientsTYNI, T; PALOTIE, A; VIINIKKA, L et al.The Journal of pediatrics. 1997, Vol 130, Num 1, pp 67-76, issn 0022-3476Article

Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screeningSYKUT-CEGIELSKA, Jolanta; GRADOWSKA, Wanda; RADOMYSKA, Barbara et al.Journal of inherited metabolic disease. 2011, Vol 34, Num 1, pp 185-195, issn 0141-8955, 11 p.Article

Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyLUND, A. M; DIXON, M. A; VREKEN, P et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 4, pp 410-412, issn 0141-8955, 3 p.Article

Docosahexaenoic acid and retinal function in children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyHARDING, C. O; GILLINGHAM, M. B; VAN CALCAR, S. C et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 3, pp 276-280, issn 0141-8955Article

Absence of the G1528C (E474Q) mutation in the α-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancyMAITRA, Anirban; DOMIATI-SAAD, Rana; YOST, Nicole et al.Pediatric research. 2002, Vol 51, Num 5, pp 658-661, issn 0031-3998Article

β-Hydroxyacyl-CoA-dehydrogenase (HADH) activity of unfrozen and frozen-thawed frog (Rana esculenta) legsPAVLOV, A; GARCIA DE FERNANDO, G. D; ORDOÑEZ, J. A et al.Journal of the science of food and agriculture. 1994, Vol 64, Num 2, pp 141-143, issn 0022-5142Article

Contribution of energy intake and tissue enzymatic profile to body weight gain in high-fat-fed ratsGAYLES, E. C; PAGLIASSOTTI, M. J; PARCH, P. A et al.American journal of physiology. Regulatory, integrative and comparative physiology. 1997, Vol 41, Num 1, pp R188-R194, issn 0363-6119Article

Calcineurin is not involved in some mitochondrial enzyme adaptations to endurance exercise training in rat skeletal muscleTERADA, Shin; NAKAGAWA, Hisashi; NAKAMURA, Yoshio et al.European journal of applied physiology. 2003, Vol 90, Num 1-2, pp 210-217, 8 p.Article

Determination of total fatty acids in plasma : Cis-5-tetradecenoic acid (C_{14 :} 1ω-9) in the diagnosis of long-chain fatty acid oxidation defectsDIVRY, P; VIANEY-SABAN, C; MATHIEU, M et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 3, pp 286-288, issn 0141-8955Article

Infection à EBV révélatrice à l'âge de 3 ans d'un déficit en 3-hydroxyacyl-CoA déshydrogénase des acides gras à chaîne longue (LCHAD) = EBV infection revealing a long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency in a 3-year-old boyDESBREE, A; HOUDON, L; TOUATI, G et al.Archives de pédiatrie (Paris). 2011, Vol 18, Num 1, pp 18-22, issn 0929-693X, 5 p.Article