Literature DB >> 2383873

Late-onset globoid cell leukodystrophy. Report on seven new patients.

A Fiumara1, L Pavone, L Siciliano, A Tinè, E Parano, G Innico.   

Abstract

During the past 12 years, ten cases of globoidcell leukodystrophy (GLD) have been followed up: seven of these patients were affected by the late infantile form. The authors point out the clinical aspects and the course of these patients and stress the high frequency of this form of GLD in Sicily.

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Year:  1990        PMID： 2383873     DOI： 10.1007/bf01850970

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN： 0256-7040            Impact factor:   1.475


  4 in total

1.  Late-onset globoid cell leucodystrophy (Krabbe's disease). Clinical and genetic delineation of two forms and their relation to the early-infantile form.

Authors:  M C Loonen; O P Van Diggelen; H C Janse; W J Kleijer; W F Arts
Journal:  Neuropediatrics       Date:  1985-08       Impact factor: 1.947

2.  Infantile and fetal globoid cell leukodystrophy: analysis of galactosylceramide and galactosylsphingosine.

Authors:  T Kobayashi; I Goto; T Yamanaka; Y Suzuki; T Nakano; K Suzuki
Journal:  Ann Neurol       Date:  1988-10       Impact factor: 10.422

3.  Globoid cell leukodystrophy: additional deficiency of psychosine galactosidase.

Authors:  T Miyatake; K Suzuki
Journal:  Biochem Biophys Res Commun       Date:  1972-08-07       Impact factor: 3.575

4.  Hydrolysis of galactosylceramide is catalyzed by two genetically distinct acid beta-galactosidases.

Authors:  T Kobayashi; N Shinnoh; I Goto; Y Kuroiwa
Journal:  J Biol Chem       Date:  1985-12-05       Impact factor: 5.157
  4 in total
  1 in total

Review 1.  The inherited leukodystrophies: a clinical overview.

Authors:  J Aicardi
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982
  1 in total

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