Literature DB >> 33417004

Metachromatic leukodystrophy with late adult-onset: diagnostic clues and differences from other genetic leukoencephalopathies with dementia.

Chiara Benzoni1, Marco Moscatelli2, Silvia Fenu3, Anna Venerando4, Ettore Salsano3,5.   

Abstract

Entities:  

Year:  2021        PMID: 33417004     DOI: 10.1007/s00415-020-10374-9

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


× No keyword cloud information.
  7 in total

1.  Late adult-onset metachromatic leukodystrophy. Dementia and polyneuropathy in a 63-year-old man.

Authors:  E P Bosch; M N Hart
Journal:  Arch Neurol       Date:  1978-07

2.  Late-presenting metachromatic leukodystrophy.

Authors:  R F Duyff; H C Weinstein
Journal:  Lancet       Date:  1996-11-16       Impact factor: 79.321

3.  Saposin B deficiency as a cause of adult-onset metachromatic leukodystrophy.

Authors:  Silvia Fenu; Barbara Castellotti; Laura Farina; Tiziana Cavallaro; Daniela Di Bella; Chiara Benzoni; Cinzia Gellera; Davide Pareyson; Franco Taroni; Ettore Salsano
Journal:  Neurology       Date:  2019-07-09       Impact factor: 9.910

Review 4.  Cerebral small vessel diseases: cerebral microangiopathies.

Authors:  E Bernd Ringelstein; Darius G Nabavi
Journal:  Curr Opin Neurol       Date:  2005-04       Impact factor: 5.710

5.  Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype.

Authors:  H Rauschka; B Colsch; N Baumann; R Wevers; M Schmidbauer; M Krammer; J-C Turpin; M Lefevre; C Olivier; S Tardieu; W Krivit; H Moser; A Moser; V Gieselmann; B Zalc; T Cox; U Reuner; A Tylki-Szymanska; F Aboul-Enein; E LeGuern; H Bernheimer; J Berger
Journal:  Neurology       Date:  2006-09-12       Impact factor: 9.910

Review 6.  Metachromatic leukodystrophy: Disease spectrum and approaches for treatment.

Authors:  Diane F van Rappard; Jaap Jan Boelens; Nicole I Wolf
Journal:  Best Pract Res Clin Endocrinol Metab       Date:  2014-10-16       Impact factor: 4.690

7.  Metachromatic leukodystrophy - mutation analysis provides further evidence of genotype-phenotype correlation.

Authors:  A Biffi; M Cesani; F Fumagalli; U Del Carro; C Baldoli; S Canale; S Gerevini; S Amadio; M Falautano; A Rovelli; G Comi; M G Roncarolo; M Sessa
Journal:  Clin Genet       Date:  2008-09-11       Impact factor: 4.438

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.