DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Myotonia
Myotonia
Spectrum of CLCN1 Mutations in Patients with Myotonia Congenita in Northern Scandinavia
Periodic Paralysis
Neuromyotonia in Hereditary Motor Neuropathy J Neurol Neurosurg Psychiatry: First Published As 10.1136/Jnnp.54.3.230 on 1 March 1991
Correlating-Phenotype-And-Genotype
What Is a Skeletal Muscle Channelopathy?
Myotonia in Centronuclear Myopathy
Clinical Approach to the Floppy Child
Hypokalemic Periodic Paralysis in Graves' Disease
Hypothyroidism with True Myotonia
An Analysis of Myotonia in Paramyotonia Congenital
Muscle Channelopathies
New Territory Opened by Periodic Paralysis Associated with Mitochondrial DNA Mutation
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
Myotonia in DNM2-Related Centronuclear Myopathy
Skeletal Muscle Channelopathies: Rare Disorders with Common Pediatric Symptoms
Channelopathies
Myotonic Disorders: a Review Article
Top View
PDF File for Your Own Personal Use
Hypokalaemic Periodic Paralysis and Myotonia in a Patient With
Differential Diagnosis of Myotonic Disorders
Myotonia Congentia (Becker & Thomsen Disease) What Is
SKELETAL MUSCLE CHANNELOPATHIES Mus7 (1)
An Overview of Congenital Myopathies Review Article Copyright © American Academy of Neurology
The Mechanism Underlying Transient Weakness in Myotonia Congenita
Familial Hyperkalemic Periodic Paralysis Caused by a De Novo Mutation in the Sodium Channel Gene SCN4A
Periodic Paralysis: What Clinician Needs to Know?
Myotonic Disorders
Neurological Channelopathies T D Graves, M G Hanna
Evaluation and Treatment of Myopathies
What Are Other Names for Myotonic Dystrophy?
A Variety of Paramyotonia Congenita by E
A Congenital Myotonic Dystrophy Type 1 Clinical Case
Familial Cramp Due to Potassium-Aggravated Myotonia
Novel Mechanisms Underlying Warm-Up and Percussion Myotonia in Myotonia Congenita
Beckers Disease
Clinical Features and Management of Some Muscular Disorders in Children -A Brief Review
Blakemore (Pdf)
Hyperkalemic Periodic Paralysis
AANEM Monograph
Periodic Paralysis Syndromes: a T3 Thyrotoxicosis Etiology
Adult Onset Myopathies Lecture Series Case Reports Invited Reviews Workshop Handouts Edxsaes/Nmsaes Case Studies Educational CD/Dvds Podcasts Practice Guidelines
Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy
Neuromuscular Guide
Molecular Biology of Distal Muscular Dystrophies - Sarcomeric Proteins on Top Bjarne Udd
Arterial-Venous Differences in Potassium Concentrations in Serum in Paramyotonia
Electrodiagnosis of Myotonic Disorders
Myotonic Disorders
The Eye in Dystrophia Myotonica* with a Report on Electromyography of the Extra-Ocular Muscles by Sidney I
Muscle Diseases.Pdf