Amanote Research

Amanote Research

    RegisterSign In

Myoglobinuria and Muscle Pain Are Common in Patients With Limb-Girdle Muscular Dystrophy 2I

Neurology - United States
doi 10.1212/wnl.0b013e3182061ad4
Full Text
Open PDF
Abstract

Available in full text

Categories
Neurology
Date

January 10, 2011

Authors
K. D. MathewsC. M. StephanK. LaubenthalT. L. WinderD. E. MicheleS. A. MooreK. P. Campbell
Publisher

Ovid Technologies (Wolters Kluwer Health)


Related search

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2I

2020English

Limb-Girdle Muscular Dystrophy

2020English

Limb Girdle Muscular Dystrophy

2008English

Lung and Respiratory Muscle Function in Limb Girdle Muscular Dystrophy.

Thorax
PulmonaryRespiratory Medicine
1994English

176. AAV-Mediated Gene Therapy in Limb-Girdle Muscular Dystrophy 2I (LGMD2I) Mouse Model

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2012English

Limb Girdle Muscular Dystrophy Type 2I: No Correlation Between Clinical Severity, Histopathology and Glycosylated Α-Dystroglycan Levels in Patients Homozygous for Common FKRP Mutation

Neuromuscular Disorders
Child HealthNeurologyPediatricsPerinatologyGenetics
2017English

Trendelenburg-Like Gait, Instability and Altered Step Patterns in a Mouse Model for Limb Girdle Muscular Dystrophy 2i

PLoS ONE
Multidisciplinary
2016English

Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1A

2020English

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2U

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy