Literature DB >> 9053552

Neuropathology of peroxisomal diseases.

J J Martin1.   

Abstract

This paper gives a description of the essential neuropathological techniques applied to the study of metabolic disorders affecting the nervous system. Subsequently, the neuropathological features of a series of peroxisomal disorders are described with special attention being paid to adrenoleukodystrophy.

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Year:  1995        PMID： 9053552     DOI： 10.1007/bf00711426

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


  40 in total

Review 1.  Peroxisomal disorders.

Authors:  H W Moser; A Bergin; D Cornblath
Journal:  Biochem Cell Biol       Date:  1991-07       Impact factor: 3.626

2.  Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase techniques: a comparison between ABC and unlabeled antibody (PAP) procedures.

Authors:  S M Hsu; L Raine; H Fanger
Journal:  J Histochem Cytochem       Date:  1981-04       Impact factor: 2.479

3.  Cortical cytoarchitectural and immunohistochemical studies on Zellweger syndrome.

Authors:  S Takashima; F Chan; L E Becker; S Houdou; Y Suzuki
Journal:  Brain Dev       Date:  1991-05       Impact factor: 1.961

4.  Neurophysiological studies in adrenomyeloneuropathy. A report on five cases.

Authors:  A Vercruyssen; J J Martin; R Mercelis
Journal:  J Neurol Sci       Date:  1982-11       Impact factor: 3.181

5.  A case of pigmentary type of orthochromatic leukodystrophy with early onset and globoid cells.

Authors:  M Taniike; H Fujimura; S Kogaki; H Tsukamoto; K Inui; M Midorikawa; J Nishimoto; S Okada
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

6.  Autopsy findings in two siblings with infantile Refsum disease.

Authors:  C W Chow; A Poulos; A J Fellenberg; J Christodoulou; D M Danks
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

7.  Zellweger syndrome amniocytes: morphological appearance and a simple sedimentation method for prenatal diagnosis.

Authors:  P B Lazarow; G M Small; M Santos; H Shio; A Moser; H Moser; A Esterman; V Black; J Dancis
Journal:  Pediatr Res       Date:  1988-07       Impact factor: 3.756

8.  Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation.

Authors:  L Van Maldergem; M Espeel; R J Wanders; F Roels; P Gerard; E Scalais; G P Mannaerts; M Casteels; Y Gillerot
Journal:  Neuromuscul Disord       Date:  1992       Impact factor: 4.296

9.  The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implications.

Authors:  J M Powers; Y Liu; A B Moser; H W Moser
Journal:  J Neuropathol Exp Neurol       Date:  1992-11       Impact factor: 3.685

10.  Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity.

Authors:  S Naidu; G Hoefler; P A Watkins; W W Chen; A B Moser; S Hoefler; N E Rance; J M Powers; M Beard; W R Green
Journal:  Neurology       Date:  1988-07       Impact factor: 9.910
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  3 in total

Review 1.  On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1997-03       Impact factor: 3.396

2.  A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency.

Authors:  G J Gerwig; E Bause; L K Nuytinck; J F Vliegenthart; W Breuer; J P Kamerling; M F Espeel; J J Martin; N W Chan; G A Dacremont
Journal:  Am J Hum Genet       Date:  2000-04-28       Impact factor: 11.025

Review 3.  Diffusion-weighted MR imaging in leukodystrophies.

Authors:  Zoltan Patay
Journal:  Eur Radiol       Date:  2005-07-15       Impact factor: 5.315
  3 in total

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