326 related articles for article (PubMed ID: 3071794)
21. Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts.
Wanders RJ; Schutgens RB; Schrakamp G; Tager JM; Van den Bosch H; Moser AB; Moser HW
J Neurol Sci; 1987 Feb; 77(2-3):331-40. PubMed ID: 3819771
[TBL] [Abstract][Full Text] [Related]
22. Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.
Wilson GN; Holmes RG; Custer J; Lipkowitz JL; Stover J; Datta N; Hajra A
Am J Med Genet; 1986 May; 24(1):69-82. PubMed ID: 3706414
[TBL] [Abstract][Full Text] [Related]
23. [Peroxisomes and peroxisomal diseases].
Petelenz M; Gonciarz Z; Grzybek H; Panz B
Postepy Hig Med Dosw; 1991; 45(1-2):77-99. PubMed ID: 1717967
[TBL] [Abstract][Full Text] [Related]
24. [The contribution of peroxisomes to lipid metabolism].
Kramar R
J Clin Chem Clin Biochem; 1986 Feb; 24(2):109-18. PubMed ID: 3711795
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.
Nguyen T; Bjorkman J; Paton BC; Crane DI
J Cell Sci; 2006 Feb; 119(Pt 4):636-45. PubMed ID: 16449325
[TBL] [Abstract][Full Text] [Related]
27. Cholesterol biosynthesis in dermal fibroblasts from patients with metabolic disorders of peroxisomal origin.
Malle E; Oettl K; Sattler W; Hoefler G; Kostner GM
Eur J Clin Invest; 1995 Jan; 25(1):59-67. PubMed ID: 7705389
[TBL] [Abstract][Full Text] [Related]
28. Clinical approach to inherited peroxisomal disorders: a series of 27 patients.
Baumgartner MR; Poll-The BT; Verhoeven NM; Jakobs C; Espeel M; Roels F; Rabier D; Levade T; Rolland MO; Martinez M; Wanders RJ; Saudubray JM
Ann Neurol; 1998 Nov; 44(5):720-30. PubMed ID: 9818927
[TBL] [Abstract][Full Text] [Related]
29. Peroxisomal abnormality in fibroblasts from involved skin of CHILD syndrome. Case study and review of peroxisomal disorders in relation to skin disease.
Emami S; Rizzo WB; Hanley KP; Taylor JM; Goldyne ME; Williams ML
Arch Dermatol; 1992 Sep; 128(9):1213-22. PubMed ID: 1519936
[TBL] [Abstract][Full Text] [Related]
30. [Liver pathologies due to peroxisome disorders].
Lovisetto P; Raviolo P
Recenti Prog Med; 1994 Feb; 85(2):134-41. PubMed ID: 8184191
[TBL] [Abstract][Full Text] [Related]
31. Analysis of peroxisomes in lymphoblasts: Zellweger syndrome and a patient with a deletion in chromosome 7.
Santos MJ; Moser AB; Drwinga H; Moser HW; Lazarow PB
Pediatr Res; 1993 May; 33(5):441-4. PubMed ID: 8511016
[TBL] [Abstract][Full Text] [Related]
32. Peroxisomal disorders.
Moser HW; Bergin A; Cornblath D
Biochem Cell Biol; 1991 Jul; 69(7):463-74. PubMed ID: 1724376
[TBL] [Abstract][Full Text] [Related]
33. Prenatal and perinatal diagnosis of peroxisomal disorders.
Schutgens RB; Schrakamp G; Wanders RJ; Heymans HS; Tager JM; van den Bosch H
J Inherit Metab Dis; 1989; 12 Suppl 1():118-34. PubMed ID: 2509803
[TBL] [Abstract][Full Text] [Related]
34. [Peroxisomal diseases--a survey].
Theron JJ; van Papendorp DH
S Afr Med J; 1996 Jun; 86(6):685-90. PubMed ID: 8764428
[TBL] [Abstract][Full Text] [Related]
35. Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.
Shimozawa N; Tsukamoto T; Suzuki Y; Orii T; Fujiki Y
J Clin Invest; 1992 Nov; 90(5):1864-70. PubMed ID: 1430210
[TBL] [Abstract][Full Text] [Related]
36. Human peroxisomal disorders.
Depreter M; Espeel M; Roels F
Microsc Res Tech; 2003 Jun; 61(2):203-23. PubMed ID: 12740827
[TBL] [Abstract][Full Text] [Related]
37. [Peroxisomal disorders; newer concept and recent studies].
Kamoshita S
Nihon Rinsho; 1990 Mar; 48(3):629-38. PubMed ID: 2192101
[No Abstract] [Full Text] [Related]
38. Diagnosis of peroxisomal disorders with neurological involvement.
Molzer B
Padiatr Padol; 1993; 28(1):43-8. PubMed ID: 8446428
[TBL] [Abstract][Full Text] [Related]
39. Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
Shimozawa N; Suzuki Y; Tomatsu S; Tsukamoto T; Osumi T; Fujiki Y; Kamijo K; Hashimoto T; Kondo N; Orii T
Pediatr Res; 1996 May; 39(5):812-5. PubMed ID: 8726233
[TBL] [Abstract][Full Text] [Related]
40. Inherited disorders of fatty alcohol metabolism.
Rizzo WB
Mol Genet Metab; 1998 Oct; 65(2):63-73. PubMed ID: 9787098
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
