ExLibris header image
SFX Logo
Title: Quantification of intramuscular fat in patients with late-onset Pompe disease by conventional magnetic resonance imaging for the long-term follow-up of enzyme replacement therapy
Source:

Plos One [1932-6203] Lollert, André yr:2018


Collapse list of basic services Basic
Full text
Full text available via PubMed Central
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Martínez, M. "Infantile-onset Pompe disease with neonatal debut: A case report and literature review." Medicine 96.51 (2017): 9186-. Link to Full Text for this item Link to SFX for this item
2. Burton, Barbara K. "The Initial Evaluation of Patients After Positive Newborn Screening: Recommended Algorithms Leading to a Confirmed Diagnosis of Pompe Disease." Pediatrics 140.Suppl 1 (2017). Link to SFX for this item
3. El Dib, Regina P. "Enzyme replacement therapy for Anderson-Fabry disease." Cochrane Database of Systematic Reviews 2.5 (2013): 11539-. Link to Full Text for this item Link to SFX for this item
4. El Dib, Regina P. "Enzyme replacement therapy for Anderson-Fabry disease." The Cochrane database of systematic reviews 5.5 (2010). Link to Full Text for this item Link to SFX for this item
5. Pfister, E-D D. "[Wilson's disease : What has been confirmed in diagnostic and therapy?]." Der Internist 58.12 (2017): 1233-1241. Link to SFX for this item
6. Varughese, S. "Diagnosis and management of Pompe disease." The South African medical journal 104.4 (2014): 273-274. Link to SFX for this item
7. Laney, Dawn A. "Fabry Disease Practice Guidelines: Recommendations of the National Society of Genetic Counselors." Journal of Genetic Counseling 22.5 (2013): 555-64. Link to SFX for this item
8. Hodson, Elisabeth M. "Antiviral medications for preventing cytomegalovirus disease in solid organ transplant recipients." Cochrane Database of Systematic Reviews 2.2 (2013). Link to Full Text for this item Link to SFX for this item
9. Sermet Gaudelus, I. "Ivacaftor treatment in patients with cystic fibrosis and the G551D-CFTR mutation." European respiratory review 22.127 (2013): 66-71. Link to Full Text for this item Link to SFX for this item
10. Chien, Y. "Algorithm for Pompe disease newborn screening: results from the Taiwan screening program." Molecular genetics and metabolism 106.3 (2012): 281-286. Link to SFX for this item
11. Ries, M. "The early clinical phenotype of Fabry disease: a study on 35 European children and adolescents." European journal of pediatrics 162.11 (2003): 767-772. Link to SFX for this item
12. Capellari, S. "Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis." Acta neuropathologica 121.1 (2010): 21-37. Link to Full Text for this item Link to SFX for this item
13. Rombach, Saskia M. "The value of estimated GFR in comparison to measured GFR for the assessment of renal function in adult patients with Fabry disease." Nephrology, Dialysis, Transplantation 25.8 (2010): 2549-2556. Link to SFX for this item
14. Wilcox, William R R. "Long-term safety and efficacy of enzyme replacement therapy for Fabry disease." American journal of human genetics 75.1 (2004): 65-74. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced