Assessing disease severity in Pompe disease: The roles of a urinary glucose tetrasaccharide biomarker and imaging techniques
Published 2012 View Full Article
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Title
Assessing disease severity in Pompe disease: The roles of a urinary glucose tetrasaccharide biomarker and imaging techniques
Authors
Keywords
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Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
Volume 160C, Issue 1, Pages 50-58
Publisher
Wiley
Online
2012-01-18
DOI
10.1002/ajmg.c.31320
References
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Related references
Note: Only part of the references are listed.- Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy
- (2011) Daniel Forsha et al. GENETICS IN MEDICINE
- Expanding the clinical spectrum of late-onset Pompe disease: Dilated arteriopathy involving the thoracic aorta, a novel vascular phenotype uncovered
- (2011) Areeg H. El-Gharbawy et al. MOLECULAR GENETICS AND METABOLISM
- Making diagnosis of Pompe disease at a presymptomatic stage: To treat or not to treat?
- (2011) K. Laloui et al. NEUROLOGY
- Whole-body muscle MRI in 20 patients suffering from late onset Pompe disease: Involvement patterns
- (2011) Robert-Yves Carlier et al. NEUROMUSCULAR DISORDERS
- High-density areas on muscle CT in childhood-onset Pompe disease are caused by excess calcium accumulation
- (2010) Keiko Ishigaki et al. ACTA NEUROPATHOLOGICA
- Pilot Study Assessing Differentiation of Steatosis Hepatis, Hepatic Iron Overload, and Combined Disease Using Two-Point Dixon MRI at 3 T: In Vitro and In Vivo Results of a 2D Decomposition Technique
- (2010) Daniel T. Boll et al. AMERICAN JOURNAL OF ROENTGENOLOGY
- Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength response
- (2010) Sabrina Ravaglia et al. JOURNAL OF INHERITED METABOLIC DISEASE
- Use of cardiac magnetic resonance imaging to evaluate cardiac structure, function and fibrosis in children with infantile Pompe disease on enzyme replacement therapy
- (2010) Piers C.A. Barker et al. MOLECULAR GENETICS AND METABOLISM
- Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopy
- (2010) Claire Wary et al. NEUROMUSCULAR DISORDERS
- A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease
- (2010) Ans T. van der Ploeg et al. NEW ENGLAND JOURNAL OF MEDICINE
- Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker
- (2009) Sarah P Young et al. GENETICS IN MEDICINE
- Enzyme replacement therapy in adult-onset glycogenosis II: Is quantitative muscle MRI helpful?
- (2009) A. Pichiecchio et al. MUSCLE & NERVE
- Screening for pompe disease using a rapid dried blood spot method: Experience of a clinical diagnostic laboratory
- (2009) Jennifer L. Goldstein et al. MUSCLE & NERVE
- Enzyme replacement therapy in severe adult-onset glycogen storage disease type II
- (2008) Sabrina Ravaglia et al. ADVANCES IN THERAPY
- Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease)
- (2008) Nomazulu Dlamini et al. NEUROMUSCULAR DISORDERS
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