140 related articles for article (PubMed ID: 9228246)
1. Peroxisomal bifunctional enzyme deficiency with associated retinal findings.
Al-Hazzaa SA; Ozand PT
Ophthalmic Genet; 1997 Jun; 18(2):93-9. PubMed ID: 9228246
[TBL] [Abstract][Full Text] [Related]
2. Peroxisomal bifunctional enzyme complex deficiency with associated retinal findings.
Eustis HS; Curry T; Superneau DW
J Pediatr Ophthalmol Strabismus; 1995; 32(2):125-7. PubMed ID: 7629669
[TBL] [Abstract][Full Text] [Related]
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; 466():365-9. PubMed ID: 10709664
[TBL] [Abstract][Full Text] [Related]
4. Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.
Kaufmann WE; Theda C; Naidu S; Watkins PA; Moser AB; Moser HW
Ann Neurol; 1996 Feb; 39(2):268-71. PubMed ID: 8967760
[TBL] [Abstract][Full Text] [Related]
5. 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; 804():750-1. PubMed ID: 8993614
[No Abstract] [Full Text] [Related]
6. 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; 235(1):176-9. PubMed ID: 9196058
[TBL] [Abstract][Full Text] [Related]
7. [Bifunctional enzyme deficiency].
Suzuki Y
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):326-7. PubMed ID: 9645073
[No Abstract] [Full Text] [Related]
8. Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome.
Itoh M; Suzuki Y; Akaboshi S; Zhang Z; Miyabara S; Takashima S
Brain Res; 2000 Mar; 858(1):40-7. PubMed ID: 10700594
[TBL] [Abstract][Full Text] [Related]
9. Peroxisomal bifunctional enzyme deficiency.
Watkins PA; Chen WW; Harris CJ; Hoefler G; Hoefler S; Blake DC; Balfe A; Kelley RI; Moser AB; Beard ME
J Clin Invest; 1989 Mar; 83(3):771-7. PubMed ID: 2921319
[TBL] [Abstract][Full Text] [Related]
10. Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis.
Wanders RJ; van Roermund CW; Brul S; Schutgens RB; Tager JM
J Inherit Metab Dis; 1992; 15(3):385-8. PubMed ID: 1357231
[No Abstract] [Full Text] [Related]
11. 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; 63(2):356-62. PubMed ID: 8725785
[TBL] [Abstract][Full Text] [Related]
12. A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities.
Wanders RJ; van Roermund CW; Schelen A; Schutgens RB; Tager JM; Stephenson JB; Clayton PT
J Inherit Metab Dis; 1990; 13(3):375-9. PubMed ID: 2122104
[No Abstract] [Full Text] [Related]
13. [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; 46(4):445-8. PubMed ID: 19213219
[TBL] [Abstract][Full Text] [Related]
14. Peroxisomal disorders: overview.
Moser HW; Moser AB
Ann N Y Acad Sci; 1996 Dec; 804():427-41. PubMed ID: 8993562
[No Abstract] [Full Text] [Related]
15. Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects.
Paton BC; Sharp PC; Crane DI; Poulos A
J Clin Invest; 1996 Feb; 97(3):681-8. PubMed ID: 8609223
[TBL] [Abstract][Full Text] [Related]
16. Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case.
Akaboshi S; Tomita Y; Suzuki Y; Une M; Sohma O; Takashima S; Takeshita K
Brain Dev; 1997 Jun; 19(4):295-9. PubMed ID: 9187482
[TBL] [Abstract][Full Text] [Related]
17. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.
Suzuki Y; Shimozawa N; Yajima S; Tomatsu S; Kondo N; Nakada Y; Akaboshi S; Lai M; Tanabe Y; Hashimoto T
Am J Hum Genet; 1994 Jan; 54(1):36-43. PubMed ID: 8279468
[TBL] [Abstract][Full Text] [Related]
18. Bifunctional protein deficiency: complementation within the same group suggesting differential enzyme defects and clues to the underlying basis.
Van Grunsven EG; van Berkel E; Lemonde H; Clayton PT; Wanders RJ
J Inherit Metab Dis; 1998 Jun; 21(3):298-301. PubMed ID: 9686380
[No Abstract] [Full Text] [Related]
19. Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
Fukuda S; Suzuki Y; Shimozawa N; Zhang Z; Orii T; Aoyama T; Hashimoto T; Kondo N
J Inherit Metab Dis; 1998 Feb; 21(1):23-8. PubMed ID: 9501266
[TBL] [Abstract][Full Text] [Related]
20. [Peroxisomal disorders--clinical and biochemical studies].
Shimozawa N; Suzuki Y; Yamaguchi S; Shimizu N; Orii T
No To Hattatsu; 1988 Nov; 20(6):480-91. PubMed ID: 3242571
[No Abstract] [Full Text] [Related]
[Next] [New Search]