Introduction: Spinal muscular atrophy is a progressive degenerative neuromuscular disease. It has several therapeutic approaches to minimize the progression of the disease. The favorable prognosis is highly dependent on the early diagnosis, from the beginning to the treatment with medications and even interventions, among them physiotherapy. Research has shown that physiotherapeutic intervention provides assistance to patient survival in a better quality of life. Objective: to measure, through a review of the literature, the physiotherapeutic interventions implemented in spinal muscular atrophy in the last ten years. Methods: literature review of articles published in the databases of the Virtual Health Library, Scielo, Pubmed, LILACS and P...
Objective: To assess the efficacy of physiotherapy interventions, including exercise therapy, for...
Neurological diseases occur in about one billion people around the world. New technologies are being...
Background: Spinal muscle atrophy (SMA) is a genetic disorder of the motor neurons resulting in musc...
Objective: The aim of the present study was to analyze through an integrative review of the techniqu...
In my bachelor work I look into the problems of the spinal muscular atrophy, assess both the effect ...
La atrofia muscular espinal (AME) es una enfermedad neuromuscular hereditaria, autosómica recesiva. ...
Objective: To assess the role of physiotherapy in approaching neuromuscular disease (NMD), with emph...
Introduction: Currently, there is no cure available for the hereditary neurodegenerative disease pro...
This paper presents a brief review of the Physical Therapy work in Myasthenia Gravis, a progressive ...
As Atrofias Musculares Espinhais (AME) fazem parte de um grupo de síndromes genéticas de herança au...
BACKGROUND AND OBJECTIVES Spinal muscular atrophy (SMA) is a progressive neuromuscular disorder a...
Introduction: Spinal muscular atrophy (SMA) is one of the most common genetically determined causes ...
The purpose of this article was to systematize available literary data and to provide general recomm...
Poleszak Julita, Szabat Przemysław, Szabat Marta, Boreński Grzegorz, Wójcik Magdalena, Milanowska Jo...
peer reviewedIntroduction: Spinal muscular atrophy (SMA) is one of the most common inherited neuromu...
Objective: To assess the efficacy of physiotherapy interventions, including exercise therapy, for...
Neurological diseases occur in about one billion people around the world. New technologies are being...
Background: Spinal muscle atrophy (SMA) is a genetic disorder of the motor neurons resulting in musc...
Objective: The aim of the present study was to analyze through an integrative review of the techniqu...
In my bachelor work I look into the problems of the spinal muscular atrophy, assess both the effect ...
La atrofia muscular espinal (AME) es una enfermedad neuromuscular hereditaria, autosómica recesiva. ...
Objective: To assess the role of physiotherapy in approaching neuromuscular disease (NMD), with emph...
Introduction: Currently, there is no cure available for the hereditary neurodegenerative disease pro...
This paper presents a brief review of the Physical Therapy work in Myasthenia Gravis, a progressive ...
As Atrofias Musculares Espinhais (AME) fazem parte de um grupo de síndromes genéticas de herança au...
BACKGROUND AND OBJECTIVES Spinal muscular atrophy (SMA) is a progressive neuromuscular disorder a...
Introduction: Spinal muscular atrophy (SMA) is one of the most common genetically determined causes ...
The purpose of this article was to systematize available literary data and to provide general recomm...
Poleszak Julita, Szabat Przemysław, Szabat Marta, Boreński Grzegorz, Wójcik Magdalena, Milanowska Jo...
peer reviewedIntroduction: Spinal muscular atrophy (SMA) is one of the most common inherited neuromu...
Objective: To assess the efficacy of physiotherapy interventions, including exercise therapy, for...
Neurological diseases occur in about one billion people around the world. New technologies are being...
Background: Spinal muscle atrophy (SMA) is a genetic disorder of the motor neurons resulting in musc...