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1987
2025

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Year Number of Results
1987 1
1989 2
1996 1
1997 1
1998 2
1999 1
2000 2
2001 4
2003 2
2004 1
2012 2
2017 1
2018 1
2024 1
2025 0

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22 results

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Page 1
Peroxisomal leukodystrophy.
Engelen M. Engelen M. Handb Clin Neurol. 2024;204:139-145. doi: 10.1016/B978-0-323-99209-1.00021-1. Handb Clin Neurol. 2024. PMID: 39322376 Review.
Peroxisomal disorders can be classified as single-enzyme deficiencies or peroxisomal biogenesis disorders (characterized by multiple peroxisomal enzyme deficiencies or complete absence of peroxisomes). ...Peroxisomal disorders associated with leukodystrophy are disc …
Peroxisomal disorders can be classified as single-enzyme deficiencies or peroxisomal biogenesis disorders (characterized by multiple …
Neonatal metabolic myopathies.
Tein I. Tein I. Semin Perinatol. 1999 Apr;23(2):125-51. doi: 10.1016/s0146-0005(99)80046-9. Semin Perinatol. 1999. PMID: 10331465 Review.
Disorders of glycogen, lipid, or mitochondrial metabolism may cause three main clinical syndromes in muscle, namely, (1) progressive weakness with hypotonia (e.g., acid maltase, debrancher enzyme, and brancher enzyme deficiencies among the glycogenoses; carnitine uptake an …
Disorders of glycogen, lipid, or mitochondrial metabolism may cause three main clinical syndromes in muscle, namely, (1) progressive weaknes …
Peroxisomal disorders: overview.
Moser HW, Moser AB. Moser HW, et al. Ann N Y Acad Sci. 1996 Dec 27;804:427-41. doi: 10.1111/j.1749-6632.1996.tb18634.x. Ann N Y Acad Sci. 1996. PMID: 8993562 Review. No abstract available.
Clinical and Laboratory Diagnosis of Peroxisomal Disorders.
Wanders RJ, Klouwer FC, Ferdinandusse S, Waterham HR, Poll-Thé BT. Wanders RJ, et al. Methods Mol Biol. 2017;1595:329-342. doi: 10.1007/978-1-4939-6937-1_30. Methods Mol Biol. 2017. PMID: 28409475 Review.
Inborn Errors of Bile Acid Metabolism.
Heubi JE, Setchell KDR, Bove KE. Heubi JE, et al. Clin Liver Dis. 2018 Nov;22(4):671-687. doi: 10.1016/j.cld.2018.06.006. Epub 2018 Aug 22. Clin Liver Dis. 2018. PMID: 30266156 Review.
Clinical consequences of defects in peroxisomal beta-oxidation.
Clayton PT. Clayton PT. Biochem Soc Trans. 2001 May;29(Pt 2):298-305. doi: 10.1042/0300-5127:0290298. Biochem Soc Trans. 2001. PMID: 11356171 Review.
The disorders of peroxisomal beta-oxidation, which have been well characterised at the molecular level, include defects of acyl-CoA oxidase, defects of the D-bifunctional protein (D-BP) (including specific defects of its enoyl-CoA hydratase and D-3-hyd …
The disorders of peroxisomal beta-oxidation, which have been well characterised at the molecular level, include defects of acyl-Co
Peroxisomal beta-oxidation and peroxisome proliferator-activated receptor alpha: an adaptive metabolic system.
Reddy JK, Hashimoto T. Reddy JK, et al. Annu Rev Nutr. 2001;21:193-230. doi: 10.1146/annurev.nutr.21.1.193. Annu Rev Nutr. 2001. PMID: 11375435 Review.
The peroxisomal beta-oxidation system consists of (a) a classical peroxisome proliferator-inducible pathway capable of catalyzing straight-chain acyl-CoAs by fatty acyl-CoA oxidase, L-bifunctional protein, and thiolase, and (b) a second noninducible pa …
The peroxisomal beta-oxidation system consists of (a) a classical peroxisome proliferator-inducible pathway capable of catalyzing straight-c …
Peroxisomal beta-oxidation and steatohepatitis.
Rao MS, Reddy JK. Rao MS, et al. Semin Liver Dis. 2001;21(1):43-55. doi: 10.1055/s-2001-12928. Semin Liver Dis. 2001. PMID: 11296696 Review.
Evidence from mice deficient in PPAR alpha (PPAR alpha-/-), deficient in peroxisomal fatty acyl-CoA oxidase (AOX-/-), the first enzyme of the classical beta-oxidation system, and deficient in both PPAR alpha and AOX (PPAR alpha-/-AOX-/-) …
Evidence from mice deficient in PPAR alpha (PPAR alpha-/-), deficient in peroxisomal fatty acyl-CoA oxidase
Prenatal and perinatal diagnosis of peroxisomal disorders.
Schutgens RB, Schrakamp G, Wanders RJ, Heymans HS, Tager JM, van den Bosch H. Schutgens RB, et al. J Inherit Metab Dis. 1989;12 Suppl 1:118-34. doi: 10.1007/BF01799291. J Inherit Metab Dis. 1989. PMID: 2509803 Review.
Peroxisomal disorders, a group of genetic diseases caused by peroxisomal dysfunction, can be classified into three groups: (1) disorders of peroxisome biogenesis with a generalized loss of peroxisomal functions (Zellweger syndrome, neonatal adrenoleukodystrophy, infantile Refsum …
Peroxisomal disorders, a group of genetic diseases caused by peroxisomal dysfunction, can be classified into three groups: (1) disorders of …
Biogenesis of peroxisomes in fetal liver.
Espeel M, Depreter M, Nardacci R, D'Herde K, Kerckaert I, Stefanini S, Roels F. Espeel M, et al. Microsc Res Tech. 1997 Dec 1;39(5):453-66. doi: 10.1002/(SICI)1097-0029(19971201)39:5<453::AID-JEMT8>3.0.CO;2-H. Microsc Res Tech. 1997. PMID: 9408912 Review.
Cytochemical (catalase and D-aminoacid oxidase activity) and immunocytochemical data in rat and human liver (antigens of catalase, the three peroxisomal beta-oxidation enzymes, alanine: glyoxylate aminotransferase, peroxisomal membrane proteins with molecular weights of 42 …
Cytochemical (catalase and D-aminoacid oxidase activity) and immunocytochemical data in rat and human liver (antigens of catalase, th …
22 results