![Physical and MRI findings in a patient with GNE myopathy presenting... | Download Scientific Diagram Physical and MRI findings in a patient with GNE myopathy presenting... | Download Scientific Diagram](https://www.researchgate.net/publication/264546085/figure/fig2/AS:619906714320896@1524808686234/Physical-and-MRI-findings-in-a-patient-with-GNE-myopathy-presenting-with-left-hand.png)
Physical and MRI findings in a patient with GNE myopathy presenting... | Download Scientific Diagram
![The unfolding spectrum of inherited distal myopathies - Milone - 2019 - Muscle & Nerve - Wiley Online Library The unfolding spectrum of inherited distal myopathies - Milone - 2019 - Muscle & Nerve - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b4453995-18ca-4c22-ab6f-af016bd0b95d/mus26332-fig-0001-m.jpg)
The unfolding spectrum of inherited distal myopathies - Milone - 2019 - Muscle & Nerve - Wiley Online Library
![Classical features of common subtypes identified. GNE myopathy (A-C):... | Download Scientific Diagram Classical features of common subtypes identified. GNE myopathy (A-C):... | Download Scientific Diagram](https://www.researchgate.net/publication/346706665/figure/fig2/AS:983475213570053@1611490171871/Classical-features-of-common-subtypes-identified-GNE-myopathy-A-C-Tibialis-anterior.png)
Classical features of common subtypes identified. GNE myopathy (A-C):... | Download Scientific Diagram
![The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews | Neurology The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews | Neurology](https://n.neurology.org/content/neurology/47/4/977/F3.large.jpg)
The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews | Neurology
![Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC - ScienceDirect Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0960896616301687-nmd3261-fig-0001.jpg)
Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC - ScienceDirect
![Markesbery Disease: Autosomal Dominant Late-Onset Distal Myopathy: From Phenotype to ZASP Gene Identification | SpringerLink Markesbery Disease: Autosomal Dominant Late-Onset Distal Myopathy: From Phenotype to ZASP Gene Identification | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12017-010-8134-6/MediaObjects/12017_2010_8134_Fig1_HTML.jpg)
Markesbery Disease: Autosomal Dominant Late-Onset Distal Myopathy: From Phenotype to ZASP Gene Identification | SpringerLink
![Frontiers | Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone Frontiers | Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone](https://www.frontiersin.org/files/Articles/436641/fneur-10-00077-HTML/image_m/fneur-10-00077-g001.jpg)
Frontiers | Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and Amiodarone
![Laing distal myopathy pathologically resembling inclusion body myositis - Roda - 2014 - Annals of Clinical and Translational Neurology - Wiley Online Library Laing distal myopathy pathologically resembling inclusion body myositis - Roda - 2014 - Annals of Clinical and Translational Neurology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/a172f497-220e-43c4-8e35-5b8c8fc5bbbf/acn3140-fig-0001-m.jpg)
Laing distal myopathy pathologically resembling inclusion body myositis - Roda - 2014 - Annals of Clinical and Translational Neurology - Wiley Online Library
![GNE myopathy: from clinics and genetics to pathology and research strategies | Orphanet Journal of Rare Diseases | Full Text GNE myopathy: from clinics and genetics to pathology and research strategies | Orphanet Journal of Rare Diseases | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13023-018-0802-x/MediaObjects/13023_2018_802_Fig1_HTML.gif)