Literature DB >> 19330222

Late-onset hexosaminidase A deficiency mimicking primary lateral sclerosis.

Clecio Godeiro-Junior1, Andre C Felicio, Vinicius Benites, Marco Antonio Chieia, Acary S B Oliveira.   

Abstract

Entities:  

Mesh：

Year:  2009        PMID： 19330222     DOI： 10.1590/s0004-282x2009000100024

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN： 0004-282X            Impact factor:   1.420


× No keyword cloud information.
  6 in total

Review 1.  Differential diagnosis of Mendelian and mitochondrial disorders in patients with suspected multiple sclerosis.

Authors:  James D Weisfeld-Adams; Ilana B Katz Sand; Justin M Honce; Fred D Lublin
Journal:  Brain       Date:  2015-01-29       Impact factor: 13.501

2.  Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease.

Authors:  Jitka Májovská; Anita Hennig; Igor Nestrasil; Susanne A Schneider; Helena Jahnová; Manuela Vaněčková; Martin Magner; Petr Dušek
Journal:  Neurol Sci       Date:  2021-11-20       Impact factor: 3.830

3.  Haematopoietic Stem Cell Transplantation Arrests the Progression of Neurodegenerative Disease in Late-Onset Tay-Sachs Disease.

Authors:  Karolina M Stepien; Su Han Lum; J Edmond Wraith; Christian J Hendriksz; Heather J Church; David Priestman; Frances M Platt; Simon Jones; Ana Jovanovic; Robert Wynn
Journal:  JIMD Rep       Date:  2017-12-07

4.  Atypical presentation of late-onset Tay-Sachs disease.

Authors:  Andres Deik; Rachel Saunders-Pullman
Journal:  Muscle Nerve       Date:  2014-02-24       Impact factor: 3.217

Review 5.  Lysosomal storage diseases.

Authors:  Carlos R Ferreira; William A Gahl
Journal:  Transl Sci Rare Dis       Date:  2017-05-25

6.  Dysarthria and Stutter as Presenting Symptoms of Late-Onset Tay-Sachs Disease in Three Siblings.

Authors:  Kristina K Grim; Gregory D Phillips; David R Renner
Journal:  Mov Disord Clin Pract       Date:  2015-06-30
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.