Incontinence in Late-Onset Pompe Disease: An Underdiagnosed Treatable Condition-Reference-Cited by-同舟云学术

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Incontinence in Late-Onset Pompe Disease: An Underdiagnosed Treatable Condition

Published:2012 Issue:2 Volume:68 Page:75-78
ISSN:1421-9913
Container-title:European Neurology
language:en
Short-container-title:Eur Neurol

Author:

Remiche Gauthier,Herbaut Anne-Geneviève,Ronchi Dario,Lamperti Costanza,Magri Francesca,Moggio Maurizio,Bresolin Nereo,Comi Giacomo P.

Publisher

S. Karger AG

Subject

Neurology (clinical),Neurology

Reference30 articles.

1. Broad spectrum of Pompe disease in patients with the same c.-32-13T->G haplotype

2. Acid a-Glucosidase Deficiency (Glycogenosis Type II, Pompe Disease)

3. The spectrum and diagnosis of acid maltase deficiency

4. Long-Term Intravenous Treatment of Pompe Disease With Recombinant Human α-Glucosidase From Milk

5. Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease

Cited by 28 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. Diagnostik, Therapie und psychosoziale Aspekte bei late-onset Morbus Pompe;Fortschritte der Neurologie · Psychiatrie;2023-07-12

2. Gut dysmotility in children with neurological impairment: the nutritional management;Frontiers in Neurology;2023-05-05

3. Multisystem presentation of Late Onset Pompe Disease: what every consulting neurologist should know;Neurologia i Neurochirurgia Polska;2023-04-28

4. Prevalence of lower urinary tract symptoms in children with early‐treated infantile‐onset Pompe disease: A single‐centre cross‐sectional study;Neurourology and Urodynamics;2022-04-28

5. New Insights into Gastrointestinal Involvement in Late-Onset Pompe Disease: Lessons Learned from Bench and Bedside;Journal of Clinical Medicine;2021-07-30

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