Article info
PDFTest yourself
Proximal muscle weakness
- Correspondence to Dr Paloma Gonzalez-Perez, MD, PhD, Department of Neurology, Harvard Medical School, Massachusetts General Hospital, Boston, MA 02114, USA; pgonzalezperez{at}partners.org
Citation
Proximal muscle weakness
Publication history
- Received January 14, 2019
- Revised February 12, 2019
- Accepted February 18, 2019
- First published April 4, 2019.
Online issue publication
June 23, 2020
Article Versions
- Previous version (23 June 2020).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Other content recommended for you
- Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations
- Metabolic myopathies: a practical approach
- Sensory neuropathy as a manifestation of multiple acyl-coenzyme A dehydrogenase deficiency
- Newborn screening for primary carnitine deficiency: who will benefit? – a retrospective cohort study
- Tandem mass spectrometry findings at autopsy for detection of metabolic disease in infant deaths: postmortem changes and confounding factors
- Progressive gait disturbance with head drop
- A diagnostic approach to recurrent myalgia and rhabdomyolysis in children
- Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry
- Do renal and cardiac malformations in the fetus signal carnitine palmitoyltransferase II deficiency? A rare lethal fatty acid oxidation defect
- 2823 MADD muscles: a case report of very-late onset multiple acyl-CoA dehydrogenase deficiency (MADD)