Intracranial aneurysm management in patients with late-onset Pompe disease (LOPD)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-020-04819-2.pdf
Reference38 articles.
1. Van der Ploeg AT, Reuser AJJ (2008) Pompe’s disease. Lancet 372:1342–1353
2. Zhang B, Zhao Y, Liu J, Li L, Shan J, Zhao D, Yan C (2016) Late-onset Pompe disease with complicated intracranial aneurysm: a Chinese case report. Neuropsychiatr Dis Treat 12:713–717
3. Papadimas G, Terzis G, Papadopoulos C, Areovimata A, Spengos K, Kavouras S, Manta P (2012) Bone density in patients with late onset Pompe disease. Int J Endocrinol Metab 10(4):599–603
4. Gaeta M, Musumeci O, Mondello S, Ruggeri P, Montagnese F, Cucinotta M, Vinci S, Milardi D, Toscano A (2015) Clinical and pathophysiological clues of respiratory dysfunction in late-onset Pompe disease: new insights from a comparative study by MRI and respiratory function assessment. Neuromuscul Disord 25(11):852–858
5. Karabul N, Skudlarek A, Berndt J et al (2014) Urge incontinence and gastrointestinal symptoms in adult patients with Pompe disease: a cross-sectional survey. JIMD Rep 17:53–61
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1. Early vascular embolization improves neurological function in patients with intracranial aneurysm;American Journal of Translational Research;2024
2. A Comprehensive Update on Late-Onset Pompe Disease;Biomolecules;2023-08-22
3. miR-139-5p Suppresses Proliferation and Angiogenesis of Intracranial Aneurysm via FGB;Journal of Healthcare Engineering;2022-04-16
4. Case Report: Identification of Compound Heterozygous Mutations in a Patient With Late-Onset Glycogen Storage Disease Type II (Pompe Disease);Frontiers in Neurology;2022-03-21
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