Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I

Journal article

Open access

Peer reviewed

K D Mathews, C M Stephan, K Laubenthal, T L Winder, D E Michele, S A Moore and K P Campbell

Neurology, Vol.76(2), pp.194-195

01/11/2011

DOI: 10.1212/WNL.0b013e3182061ad4

PMCID: PMC3030231

PMID: 21220724

Files and links (1)

url

https://europepmc.org/articles/pmc3030231View

Published (Version of record) Open Access

no abstract | clinical/scientific notes

Mutation

Diagnosis, Differential

Muscular Dystrophies, Limb-Girdle - diagnosis

Humans

Muscular Dystrophies, Limb-Girdle - physiopathology

Muscles - physiopathology

Male

Incidence

Myoglobinuria - genetics

Proteins - genetics

Young Adult

Pain - genetics

Muscular Dystrophies, Limb-Girdle - genetics

Pain - physiopathology

Adolescent

Adult

Female

Myoglobinuria - physiopathology

Retrospective Studies

Child

Title: Subtitle: Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I
Creators: K D Mathews - Department of Pediatrics, University of Iowa, Iowa City, IA, USA. katherine-mathews@uiowa.edu
C M Stephan
K Laubenthal
T L Winder
D E Michele
S A Moore
K P Campbell
Resource Type: Journal article
Publication Details: Neurology, Vol.76(2), pp.194-195
DOI: 10.1212/WNL.0b013e3182061ad4
PMID: 21220724
PMCID: PMC3030231
NLM abbreviation: Neurology
ISSN: 0028-3878
eISSN: 1526-632X
Publisher: United States
Grant note: Howard Hughes Medical Institute U54 NS053672 / NINDS NIH HHS UL1 RR024979 / NCRR NIH HHS
Language: English
Date published: 01/11/2011
Academic Unit: Neurology; Molecular Physiology and Biophysics; Stead Family Department of Pediatrics; Pathology; Iowa Neuroscience Institute; Neurology (Pediatrics)
Record Identifier: 9984020649202771

18 Record Views