The frequency of late-onset Pompe disease in pediatric patients with limb-girdle muscle weakness and nonspecific hyperCKemia: A multicenter study-Reference-Cited by-同舟云学术

The frequency of late-onset Pompe disease in pediatric patients with limb-girdle muscle weakness and nonspecific hyperCKemia: A multicenter study

Published:2016-11 Issue:11 Volume:26 Page:796-800
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Ünver Olcay,Hacıfazlıoğlu Nilüfer Eldeş,Karatoprak Elif,Güneş Ayfer Sakarya,Sağer Güneş,Kutlubay Büşra,Sözen Gülhan,Saltık Sema,Yılmaz Kutluhan,Kara Bülent,Türkdoğan Dilşad

Funder

Genzyme

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference31 articles.

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3. The natural course of non-classic Pompe's disease; a review of 225 published cases;Winkel;J Neurol,2005

4. Decompensated cor pulmonaleas the first manifestation of adult-onset myopathy;Kurz;Respiration,1998

5. Clinical variability in adult-onset acid maltase deficiency: report of affected sibs and review of the literature;Felice;Medicine (Baltimore),1995

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