Cardiovascular disease in non-classic Pompe disease: A systematic review-Reference-Cited by-同舟云学术

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Cardiovascular disease in non-classic Pompe disease: A systematic review

Published:2021-02 Issue:2 Volume:31 Page:79-90
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

van Kooten H.A.,Roelen C.H.A.,Brusse E.,van der Beek N.A.M.E.,Michels M.,van der Ploeg A.T.,Wagenmakers M.A.E.M.,van Doorn P.A.

Funder

Erasmus MC Vriendenfonds

Publisher

Elsevier BV

Subject

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

Reference104 articles.

1. Pompe's disease;van der Ploeg;Lancet,2008

2. The natural course of infantile Pompe's disease: 20 Original cases compared with 133 cases from the literature;Van den Hout;Pediatrics,2003

3. Pompe disease (glycogen storage disease type II): clinical features and enzyme replacement therapy;Van der Beek NAME;Acta Neurol Belg,2006

4. The emerging phenotype of late-onset Pompe disease: a systematic literature review;Chan;Mol Genet Metab,2017

5. Multisystem late onset Pompe disease (LOPD): an update on clinical aspects;Toscano;Ann Transl Med,2019

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Intracranial vasculopathy: an important organ damage in young adult patients with late-onset Pompe disease;Orphanet Journal of Rare Diseases;2024-07-15

2. Interplay between mitochondrial dysfunction and lysosomal storage: challenges in genetic metabolic muscle diseases with a focus on infantile onset Pompe disease;Frontiers in Cardiovascular Medicine;2024-02-20

3. Cardiomyopathies – Inherited subtypes and phenocopies;Genomic and Molecular Cardiovascular Medicine;2024

4. Long-term benefits of physical activity in adult patients with late onset Pompe disease: a retrospective cohort study with 10 years of follow-up;Orphanet Journal of Rare Diseases;2023-10-11

5. Variant Classification for Pompe disease; ACMG/AMP specifications from the ClinGen Lysosomal Diseases Variant Curation Expert Panel;Molecular Genetics and Metabolism;2023-09

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