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Calpainopathy
107Th ENMC International Workshop: the Management of Cardiac Involvement in Muscular Dystrophy and Myotonic Dystrophy
The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies Review Article
Clinical Variability in Calpainopathy: What Makes the Difference?
Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations
The Congenital and Limb-Girdle Muscular Dystrophies Sharpening the Focus, Blurring the Boundaries
ACTA MYOLOGICA (Myopathies, Cardiomyopathies and Neuromyopathies)
Noncyclic Chronic Pelvic Pain Therapies for Women: Comparative Effectiveness Comparative Effectiveness Review Number 41
Mutational Spectrum of Autosomal Recessive Limb-Girdle Muscular Dystrophies in a Cohort of 112 Iranian Patients and Reporting Of
Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent
Camptocormia As the Presenting Symptom in Sporadic Late Onset Nemaline Myopathy: a Case Report Matthias Türk1* , Armin M
Molecular and Cellular Basis of Calpainopathy (Limb Girdle Muscular Dystrophy Type 2A) ⁎ Irina Kramerova A, Jacques S
Diagnosis and Treatment of Limb-Girdle Muscular Dystrophy
Approach to Myopathy Introduction
Preliminary Pages.P65
Evaluation and Treatment of Myopathies
Circulating Mir-206 As a Biomarker for Patients Affected by Severe Limb Girdle Muscle Dystrophies
Translational Research Studies in Exercise-Related Muscle Disorders
Neurology Curriculum 2010 (With 2013 Amendments) Item Review Article Case Report Title 1
Top View
Original Article Semi-Quantitative Assessment of Lower Limb MRI in Dystrophinopathy
A Promising Future for Stem-Cell-Based Therapies in Muscular Dystrophies—In Vitro and in Vivo Treatments to Boost Cellular Engraftment
Therapeutic Possibilities in the Autosomal Recessive Limb-Girdle Muscular Dystrophies
Myopathies Crossfires
MYOPATHY Evaluation and Diagnosis- Kirsten Gruis, MD 2010
Muscle Pathology in 31 Patients with Calpain 3 Gene Mutations Zmiany Histopatologiczne W Biopsji Miêœnia U 31 Chorych Z Mutacjami W Genie Koduj¹cym Kalpainê 3
FAQ for Patients and Families
List for Testing Done out of Québec LABORATOIRE CLINIQUES CUSM MUHC CLINICAL LABS
ACTA MYOLOGICA (Myopathies, Cardiomyopathies and Neuromyopathies)
The Relative Frequency of Common Neuromuscular Diagnoses in a Reference Center
Adult Onset Myopathies Lecture Series Case Reports Invited Reviews Workshop Handouts Edxsaes/Nmsaes Case Studies Educational CD/Dvds Podcasts Practice Guidelines
How to Go About Diagnosing and Managing the Limb-Girdle Muscular Dystrophies
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Facial Weakness in Heterozygous Carriers of Calpain3 Mutation
229Th ENMC International Workshop: Limb Girdle Muscular Dystrophies – Nomenclature and Reformed Classification Naarde
ACTA MYOLOGICA (Myopathies, Cardiomyopathies and Neuromyopathies)
A Clinical Approach to Muscle Diseases
Limb Girdle Muscular Dystrophy Type 2A) Irina Kramerova, Jacques S
Myopathy with Contractures