231 related articles for article (PubMed ID: 3652452)
1. Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders.
Wanders RJ; van Wijland MJ; van Roermund CW; Schutgens RB; van den Bosch H; Tager JM; Nijenhuis A; Tromp A
Clin Chim Acta; 1987 Jun; 165(2-3):303-10. PubMed ID: 3652452
[TBL] [Abstract][Full Text] [Related]
2. Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.
Wanders RJ; van Roermund CW; van Wijland MJ; Heikoop J; Schutgens RB; Schram AW; Tager JM; van den Bosch H; Poll-Thé BT; Saudubray JM
Clin Chim Acta; 1987 Jul; 166(2-3):255-63. PubMed ID: 2441904
[TBL] [Abstract][Full Text] [Related]
3. Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.
Wanders RJ; van Roermund CW; van Wijland MJ; Schutgens RB; Heikoop J; van den Bosch H; Schram AW; Tager JM
J Clin Invest; 1987 Dec; 80(6):1778-83. PubMed ID: 3680527
[TBL] [Abstract][Full Text] [Related]
4. Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids.
Aubourg P; Kremser K; Roland MO; Rocchiccioli F; Singh I
Pediatr Res; 1993 Sep; 34(3):270-6. PubMed ID: 7510868
[TBL] [Abstract][Full Text] [Related]
5. Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts.
Wanders RJ; Denis S; Ruiter JP; Schutgens RB; van Roermund CW; Jacobs BS
J Inherit Metab Dis; 1995; 18 Suppl 1():113-24. PubMed ID: 9053546
[TBL] [Abstract][Full Text] [Related]
6. Peroxisomal beta-oxidation of polyunsaturated long chain fatty acids in human fibroblasts. The polyunsaturated and the saturated long chain fatty acids are retroconverted by the same acyl-CoA oxidase.
Christensen E; Woldseth B; Hagve TA; Poll-The BT; Wanders RJ; Sprecher H; Stokke O; Christophersen BO
Scand J Clin Lab Invest Suppl; 1993; 215():61-74. PubMed ID: 8327852
[TBL] [Abstract][Full Text] [Related]
7. Immunochemical and biochemical studies of fatty acid oxidation in fibroblasts of Zellweger and X-linked adrenoleukodystrophy patients.
Reubsaet FA; Veerkamp JH; Brückwilder ML; Trijbels JM; Hashimoto T; Monnens LA
Biochim Biophys Acta; 1991 Jun; 1083(3):305-9. PubMed ID: 2049396
[TBL] [Abstract][Full Text] [Related]
8. Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy.
Chen WW; Watkins PA; Osumi T; Hashimoto T; Moser HW
Proc Natl Acad Sci U S A; 1987 Mar; 84(5):1425-8. PubMed ID: 3469675
[TBL] [Abstract][Full Text] [Related]
9. X-linked adrenoleukodystrophy: defective peroxisomal oxidation of very long chain fatty acids but not of very long chain fatty acyl-CoA esters.
Wanders RJ; van Roermund CW; van Wijland MJ; Nijenhuis AA; Tromp A; Schutgens RB; Brouwer-Kelder EM; Schram AW; Tager JM; van den Bosch H
Clin Chim Acta; 1987 Jun; 165(2-3):321-9. PubMed ID: 3652454
[TBL] [Abstract][Full Text] [Related]
10. Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies.
Schutgens RB; Wanders RJ; Nijenhuis A; van den Hoek CM; Heymans HS; Schrakamp G; Bleeker-Wagemakers EM; Delleman JW; Schram AW; Tager JM
Enzyme; 1987; 38(1-4):161-76. PubMed ID: 3440444
[TBL] [Abstract][Full Text] [Related]
11. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
Poll-The BT; Roels F; Ogier H; Scotto J; Vamecq J; Schutgens RB; Wanders RJ; van Roermund CW; van Wijland MJ; Schram AW
Am J Hum Genet; 1988 Mar; 42(3):422-34. PubMed ID: 2894756
[TBL] [Abstract][Full Text] [Related]
12. Immunoblot detection of enzyme proteins of peroxisomal beta-oxidation in fibroblasts, amniocytes, and chorionic villous cells. Possible marker for prenatal diagnosis of Zellweger's syndrome.
Shimozawa N; Suzuki Y; Orii T; Hashimoto T
Prenat Diagn; 1988 May; 8(4):287-90. PubMed ID: 3041403
[TBL] [Abstract][Full Text] [Related]
13. The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.
Moser AE; Singh I; Brown FR; Solish GI; Kelley RI; Benke PJ; Moser HW
N Engl J Med; 1984 May; 310(18):1141-6. PubMed ID: 6709009
[TBL] [Abstract][Full Text] [Related]
14. Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation.
Van Maldergem L; Espeel M; Wanders RJ; Roels F; Gerard P; Scalais E; Mannaerts GP; Casteels M; Gillerot Y
Neuromuscul Disord; 1992; 2(3):217-24. PubMed ID: 1483048
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of inborn errors in peroxisomal beta-oxidation.
Wanders RJ; Schutgens RB; van den Bosch H; Tager JM; Kleijer WJ
Prenat Diagn; 1991 Apr; 11(4):253-61. PubMed ID: 1896411
[TBL] [Abstract][Full Text] [Related]
16. Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment.
Schutgens RB; Wanders RJ; Heymans HS; Schram AW; Tager JM; Schrakamp G; van den Bosch H
J Inherit Metab Dis; 1987; 10 Suppl 1():33-45. PubMed ID: 3119940
[TBL] [Abstract][Full Text] [Related]
17. Biochemical abnormalities in rhizomelic chondrodysplasia punctata.
Hoefler G; Hoefler S; Watkins PA; Chen WW; Moser A; Baldwin V; McGillivary B; Charrow J; Friedman JM; Rutledge L
J Pediatr; 1988 May; 112(5):726-33. PubMed ID: 2452243
[TBL] [Abstract][Full Text] [Related]
18. Metabolism of saturated and polyunsaturated very-long-chain fatty acids in fibroblasts from patients with defects in peroxisomal beta-oxidation.
Street JM; Singh H; Poulos A
Biochem J; 1990 Aug; 269(3):671-7. PubMed ID: 2117919
[TBL] [Abstract][Full Text] [Related]
19. Accumulation and defective beta-oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants.
Poulos A; Singh H; Paton B; Sharp P; Derwas N
Clin Genet; 1986 May; 29(5):397-408. PubMed ID: 2427264
[TBL] [Abstract][Full Text] [Related]
20. Peroxisomal beta-oxidation of branched chain fatty acids in human skin fibroblasts.
Singh H; Brogan M; Johnson D; Poulos A
J Lipid Res; 1992 Nov; 33(11):1597-605. PubMed ID: 1464743
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
