Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease-Reference-Cited by-同舟云学术

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Causally treatable, hereditary neuropathies in Fabry's disease, transthyretin-related familial amyloidosis, and Pompe's disease

Published:2017-03-12 Issue:6 Volume:136 Page:558-569
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:Acta Neurol Scand

Author:

Finsterer J.¹^ORCID,Wanschitz J.²,Quasthoff S.³,Iglseder S.⁴,Löscher W.²,Grisold W.⁵

Affiliation:

1. Krankenanstalt Rudolfstiftung; Vienna Austria

2. Department of Neurology; Medical University Innsbruck; Innsbruck Austria

3. Department of Neurology; Medical University Graz; Graz Austria

4. Neurological Department; KH Barmherzige Brüder; Linz Austria

5. Neurological Department; Kaiser-Franz Josef Spital; Vienna Austria

Publisher

Wiley

Subject

Clinical Neurology,Neurology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ane.12758/fullpdf

Reference108 articles.

1. Inherited neuropathies: clinical overview and update;Klein;Muscle Nerve,2013

2. Fabry disease;Germain;Orphanet J Rare Dis,2010

3. Acute progression of neuromuscular findings in infantile Pompe disease;Burrow;Pediatr Neurol,2010

4. The diagnostic accuracy of Sudoscan in transthyretin familial amyloid polyneuropathy;Castro;Clin Neurophysiol,2016

5. Fabry's disease: case series and review of literature;Wani;Ann Med Health Sci Res,2016

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4. Clinical examination of patients with late-onset Pompe disease: typical and not typical symptoms and signs;Neuromuscular Diseases;2020-01-10

5. S1-Leitlinie: Diagnostik bei Polyneuropathien;DGNeurologie;2019-07-12

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