A motor point stimulation protocol was carried out on the tibialis anterior of myotonic dystrophy (MyD) patients. The surface myoelectric signal was monitored to record average rectified value (ARV), median frequency of power spectrum (MDF), and conduction velocity (CV) parameters. The ARV curve showed a decreasing trend that reveals a reduction in the M-wave amplitude during stimulation. MDF presented a significant decrement in the first seconds of sustained contraction, probably caused by abnormal lengthening of the depolarization zone. CV was significantly lower in patients, suggesting reduced mean fiber size
Patients with autosomal recessive generalized myotonia, or Pecker's disease, often suffer from a pec...
INTRODUCTION Myotonia in myotonic dystrophy types 1 (DM1) and 2 (DM2) is generally attributed to ...
At medium and high force levels, patients with generalized myotonia (GM) cannot produce normal force...
We performed a motor point stimulation protocol on tibialis anterior of MyD patients and recorded fo...
Objectives: To apply surface electromyography (EMG) using low and high stimulation frequencies, to e...
The dimensional changes of the muscle fibres of the active motor units generate a signal, labelled a...
In myotonic dystrophy alteration in membrane excitability characterizes, in addition to the dystroph...
Abstract: Myotonic dystrophy is the most common form of muscular dystrophy in adults. Both subtypes,...
SYNOPSIS Changes in amplitude of the evoked muscle action potential (MAP) have been observed in four...
Patients with autosomal recessive generalized myotonia, or Becker's disease, often suffer from a pec...
Aim: Clinical manifestations of myotonic dystrophy type 1 (DM1) involve myotonia and progressive mus...
The partitioning of the electromechanical delay by an electromyographic (EMG), mechanomyographic (MM...
The electromechanical delay during muscle contraction and relaxation can be partitioned into mainly ...
Objectives: Weakness and fatigue are frequent symptoms in myotonic dystrophy type 1 (DM1), mainly as...
ABSTRACT- In myotonic dystrophy (MD), disease severity has been correlated with expansion of CTG rep...
Patients with autosomal recessive generalized myotonia, or Pecker's disease, often suffer from a pec...
INTRODUCTION Myotonia in myotonic dystrophy types 1 (DM1) and 2 (DM2) is generally attributed to ...
At medium and high force levels, patients with generalized myotonia (GM) cannot produce normal force...
We performed a motor point stimulation protocol on tibialis anterior of MyD patients and recorded fo...
Objectives: To apply surface electromyography (EMG) using low and high stimulation frequencies, to e...
The dimensional changes of the muscle fibres of the active motor units generate a signal, labelled a...
In myotonic dystrophy alteration in membrane excitability characterizes, in addition to the dystroph...
Abstract: Myotonic dystrophy is the most common form of muscular dystrophy in adults. Both subtypes,...
SYNOPSIS Changes in amplitude of the evoked muscle action potential (MAP) have been observed in four...
Patients with autosomal recessive generalized myotonia, or Becker's disease, often suffer from a pec...
Aim: Clinical manifestations of myotonic dystrophy type 1 (DM1) involve myotonia and progressive mus...
The partitioning of the electromechanical delay by an electromyographic (EMG), mechanomyographic (MM...
The electromechanical delay during muscle contraction and relaxation can be partitioned into mainly ...
Objectives: Weakness and fatigue are frequent symptoms in myotonic dystrophy type 1 (DM1), mainly as...
ABSTRACT- In myotonic dystrophy (MD), disease severity has been correlated with expansion of CTG rep...
Patients with autosomal recessive generalized myotonia, or Pecker's disease, often suffer from a pec...
INTRODUCTION Myotonia in myotonic dystrophy types 1 (DM1) and 2 (DM2) is generally attributed to ...
At medium and high force levels, patients with generalized myotonia (GM) cannot produce normal force...