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Muscular dystrophy
This Letter Is for Families with Variant(S) in the Titin Gene, Also
The Myotonic Dystrophies: Diagnosis and Management Chris Turner,1 David Hilton-Jones2
Skeletal Muscle Channelopathies: a Guide to Diagnosis and Management
Evidence-Based Guideline: Evaluation, Diagnosis, and Management Of
Myopathies Infosheet
Clinical Approach to the Floppy Child
Blueprint Genetics Comprehensive Muscular Dystrophy / Myopathy Panel
Duchenne and Becker Muscular Dystrophy
AMERICAN ACADEMY of PEDIATRICS Cardiovascular
Muscular Dystrophies: What the Radiologist Should Know
Myotonic Dystrophy Type 2
Epidemiological Study and Genetic Characterization of Inherited Muscle
The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease
Patients with Genetically Confirmed IBMPFD Were Identified
Myotonic Dystrophy
Cognitive Deficits in Myopathies
Diagnosis of a Centronuclear Myopathy Case in Appalachia 20 Years from Symptom Onset Christopher Burrell BS1, Zachary Wilson DO2, Dominika Lozowska MD Bsc1
Duchenne and Becker Muscular Dystrophy) Policy Number: PG0411 ADVANTAGE | ELITE | HMO Last Review: 07/09/2019
Top View
Skeletal Muscle Channelopathies: Rare Disorders with Common Pediatric Symptoms
Muscular Dystrophy: a Public Health Challenge Muscular Dystrophy Public Health Need
PDF-Document
Muscular Dystrophy N
Muscular Dystrophy Interagency Collaboration
Facioscapulohumeral Muscular Dystrophy
A PDF of the Occupational Therapy Guidelines
Diagnosis and Management of Duchenne Muscular Dystrophy, Part 1
Facts About Myopathies Dear Friends: Hen I Was in My Early Teens, WI Was Having an Ice Cream at the Mall with Some Friends, and Suddenly I Couldn’T Move a Muscle
What Is Becker Muscular Dystrophy?
Differential Diagnosis of Myotonic Disorders
A Guide for Families Family Guide 1 // 64 2 // 64 Family Guide
Clinical and Pathological Study Ofa Case of Congenital Muscular Dystrophy
A Diagnostic Service for Rare Neuromuscular Disorders (All Ages)
Duchenne and Becker Muscular Dystrophy
Basic Information for Midwives
Diagnosis and Treatment of Limb-Girdle Muscular Dystrophy
Miyoshi Myopathy
An Overview of Congenital Myopathies Review Article Copyright © American Academy of Neurology
Facioscapulohumeral Muscular Dystrophy
BECKER MUSCULAR DYSTROPHY Becker Muscular Dystrophy
MUSCULAR DYSTROPHY Date of Publication: Dec
Neuromuscular Disorders
Neurological Channelopathies T D Graves, M G Hanna
Myotonic Dystrophy Type 1 (Steinert's Disease)
Duchenne Muscular Dystrophy and Related Dystrophinopathies: Developing Drugs for Treatment Guidance for Industry
Dystrophinopathies, Including Duchenne and Becker Muscular Dystrophies and X-Linked Dilated Cardiomyopathy
Duchenne Muscular Dystrophy Fact Sheet
Nemaline (Rod) Myopathies
Muscular Dystrophies Sathasivam S
Nemaline Myopathy (NM) Is an Inherited Neuromuscular Disease Characterized by Muscle Weakness And
Facioscapulohumeral Muscular Dystrophy (FSHD) Fact Sheet
Duchenne Muscular Dystrophy
Skeletal Muscle Channelopathies – a Guide to Diagnosis and Management
Skeletal Muscles
Myotubular Centronuclear Myopathy
MDA FSHD Fact Sheet June 2019
Comprehensive List of Neuromuscular Disorders Covered by Muscular Dystrophy Canada
Congenital Myopathy Infosheet 6-10-19
What Is Myotonic Dystrophy?
Facioscapulohumeral Muscular Dystrophy
Adult Onset Myopathies Lecture Series Case Reports Invited Reviews Workshop Handouts Edxsaes/Nmsaes Case Studies Educational CD/Dvds Podcasts Practice Guidelines
Duchenne Muscular Dystrophy (DMD
Hypotonia – Part 1
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Nemaline Myopathies: a Current View
Nemaline Myopathy, NEB-Related
Diagnosis of Duchenne Muscular Dystrophy in a Presymptomatic Infant Using Next-Generation Sequencing and Chromosomal Microarray Analysis: a Case Report
Neuromuscular Guide
X-Linked Myotubular Myopathy And
Neuromuscular Disorders
Molecular Biology of Distal Muscular Dystrophies - Sarcomeric Proteins on Top Bjarne Udd
Anaesthetic Management of Patients with Myopathies
Electrodiagnosis of Myotonic Disorders
Laboratory Abnormalities in Patients with Myotonic Dystrophy Type 2
Duchenne Muscular Dystrophy (DMD)
Physical Therapy
Facioscapulohumeral Muscular Dystrophy