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3. D-hydroxyacyl-CoA dehydrogenase deficiency. Identification of a new peroxisomal disorder with implications for other disorders of beta-oxidation. van Grunsven EG, van Berkel E, Denis S, Mooijer PA, Wanders RJ. Adv Exp Med Biol; 1999 Feb; 466():365-9. PubMed ID: 10709664 [Abstract] [Full Text] [Related]
4. Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme protein. van Grunsven EG, van Roermund CW, Denis S, Wanders RJ. Biochem Biophys Res Commun; 1997 Jun 09; 235(1):176-9. PubMed ID: 9196058 [Abstract] [Full Text] [Related]
5. Urinary bile acids and peroxisomal bifunctional enzyme deficiency. Natowicz MR, Evans JE, Kelley RI, Moser AB, Watkins PA, Moser HW. Am J Med Genet; 1996 May 17; 63(2):356-62. PubMed ID: 8725785 [Abstract] [Full Text] [Related]
6. Peroxisomal bifunctional enzyme deficiency with associated retinal findings. Al-Hazzaa SA, Ozand PT. Ophthalmic Genet; 1997 Jun 17; 18(2):93-9. PubMed ID: 9228246 [Abstract] [Full Text] [Related]
7. [Peroxisomal disorders]. Suzuki Y, Shimozawa N, Imamura A, Kondo N. Ryoikibetsu Shokogun Shirizu; 2000 Jun 17; (29 Pt 4):452-9. PubMed ID: 11031991 [No Abstract] [Full Text] [Related]
8. Biochemical findings in a series of Australian patients with isolated defects in peroxisomal beta-oxidation. Paton BC, Sharp PC, Poulos A. Ann N Y Acad Sci; 1996 Dec 27; 804():750-1. PubMed ID: 8993614 [No Abstract] [Full Text] [Related]
9. [Peroxisomal D-bifunctional enzyme deficiency. A case report]. Chávez-Torres R, Ruiz-Chávez J, Ruiz-Cruz E, Juárez-Naranjo E, Campos-Campos L, Villanueva-Padrón L, Horta-Martínez A, Montes-Castillo Mde L, Monroy-Hernández V, Hernández-Caballero E. Rev Med Inst Mex Seguro Soc; 2008 Dec 27; 46(4):445-8. PubMed ID: 19213219 [Abstract] [Full Text] [Related]