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

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

Available in full text

Categories
Neurology
Date
Authors
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

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy