Literature DB >> 7807942

A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblasts.

R B Schutgens1, R J Wanders, C Jakobs, M Arslan-Kirchner, K Miller, P Wieacker, D Hunnemann, P Hurter, M von Schutz.   

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Year:  1994        PMID: 7807942     DOI: 10.1007/bf00711818

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


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  9 in total

Review 1.  Biochemistry of peroxisomes.

Authors:  H van den Bosch; R B Schutgens; R J Wanders; J M Tager
Journal:  Annu Rev Biochem       Date:  1992       Impact factor: 23.643

2.  Bile acids in peroxisomal disorders.

Authors:  J R Van Eldere; G G Parmentier; H J Eyssen; R J Wanders; R B Schutgens; J Vamecq; F Van Hoof; B T Poll-The; J M Saudubray
Journal:  Eur J Clin Invest       Date:  1987-10       Impact factor: 4.686

3.  Deficiency of acyl-CoA:dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test.

Authors:  R J Wanders; G van Weringh; G Schrakamp; J M Tager; H van den Bosch; R B Schutgens
Journal:  Clin Chim Acta       Date:  1985-10-15       Impact factor: 3.786

4.  Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals.

Authors:  I Björkhem; L Sisfontes; B Boström; B F Kase; R Blomstrand
Journal:  J Lipid Res       Date:  1986-07       Impact factor: 5.922

Review 5.  Postnatal diagnosis of peroxisomal disorders: a biochemical approach.

Authors:  R J Wanders; R B Schutgens; P G Barth; J M Tager; H van den Bosch
Journal:  Biochimie       Date:  1993       Impact factor: 4.079

6.  Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.

Authors:  G Schrakamp; C G Schalkwijk; R B Schutgens; R J Wanders; J M Tager; H van den Bosch
Journal:  J Lipid Res       Date:  1988-03       Impact factor: 5.922

7.  Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata.

Authors:  R B Schutgens; I W Bouman; A A Nijenhuis; R J Wanders; M E Frumau
Journal:  Clin Chem       Date:  1993-08       Impact factor: 8.327

8.  Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome.

Authors:  E M Bleeker-Wagemakers; J W Oorthuys; R J Wanders; R B Schutgens
Journal:  Clin Genet       Date:  1986-02       Impact factor: 4.438

9.  A milder variant of Zellweger syndrome.

Authors:  P G Barth; R B Schutgens; J A Bakkeren; K P Dingemans; H S Heymans; A C Douwes; J M van der Klei-van Moorsel
Journal:  Eur J Pediatr       Date:  1985-11       Impact factor: 3.183

  9 in total
  4 in total

1.  Immunocytochemical localization of peroxisomal proteins in human liver and kidney.

Authors:  M Espeel; G Van Limbergen
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 2.  Diagnostic work-up of a peroxisomal patient.

Authors:  J G Leroy; M Espeel; J F Gadisseux; H Mandel; M Martinez; B T Poll-The; R J Wanders; F Roels
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

3.  Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients.

Authors:  R J Wanders; C Dekker; R Ofman; R B Schutgens; P Mooijer
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 4.  Clinical approach to inherited peroxisomal disorders.

Authors:  F Poggi-Travert; B Fournier; B T Poll-The; J M Saudubray
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

  4 in total

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