Literature DB >> 17190962

Ptosis as a feature of late-onset glycogenosis type II.

W B Groen1, W G Leen, A M C Vos, J R M Cruysberg, P A van Doorn, B G M van Engelen.   

Abstract

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Year:  2006        PMID： 17190962     DOI： 10.1212/01.wnl.0000249183.39952.3e

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  3 in total

1.  Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study.

Authors:  Nadine A M E van der Beek; Juna M de Vries; Marloes L C Hagemans; Wim C J Hop; Marian A Kroos; John H J Wokke; Marianne de Visser; Baziel G M van Engelen; Jan B M Kuks; Anneke J van der Kooi; Nicolette C Notermans; Karin G Faber; Jan J G M Verschuuren; Arnold J J Reuser; Ans T van der Ploeg; Pieter A van Doorn
Journal:  Orphanet J Rare Dis       Date:  2012-11-12       Impact factor: 4.123

2.  Phenotypical variation within 22 families with Pompe disease.

Authors:  Stephan C A Wens; Carin M van Gelder; Michelle E Kruijshaar; Juna M de Vries; Nadine A M E van der Beek; Arnold J J Reuser; Pieter A van Doorn; Ans T van der Ploeg; Esther Brusse
Journal:  Orphanet J Rare Dis       Date:  2013-11-19       Impact factor: 4.123

3.  Childhood Pompe disease: clinical spectrum and genotype in 31 patients.

Authors:  C I van Capelle; J C van der Meijden; J M P van den Hout; J Jaeken; M Baethmann; T Voit; M A Kroos; T G J Derks; M E Rubio-Gozalbo; M A Willemsen; R H Lachmann; E Mengel; H Michelakakis; J C de Jongste; A J J Reuser; A T van der Ploeg
Journal:  Orphanet J Rare Dis       Date:  2016-05-18       Impact factor: 4.123
  3 in total

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