Lista de obras - Birgit F Steffensen - Dominio Público Uruguay

206th ENMC International Workshop: Care for a novel group of patients - adults with Duchenne muscular dystrophy Naarden, The Netherlands, 23-25 May 2014.

artículo científico publicado en 2015

A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy.

artículo científico publicado en 2000

Adult life with Duchenne muscular dystrophy: observations among an emerging and unforeseen patient population.

artículo científico publicado en 2005

Change in muscle strength over time in spinal muscular atrophy types II and III. A long-term follow-up study.

artículo científico publicado en 2012

Developing and maintaining of user-defined personal competencies among young adults with congenital physical disability

artículo científico publicado en 2008

Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale.

artículo científico publicado en 2013

Fracture risk in patients with muscular dystrophy and spinal muscular atrophy

scientific article published on 01 July 2001

Functional assessment for people unable to walk due to spinal muscular atrophy and Duchenne muscular dystrophy. Translation and validation of the Egen Klassifikation 2 scale for the Spanish population

artículo científico publicado en 2015

Indicators of need for mechanical ventilation in Duchenne muscular dystrophy and spinal muscular atrophy

artículo científico publicado en 1995

Life quality of patients with muscular failure, using permanent respiratory support, seen from their point of view. 1. Information, choice and quality of life

artículo científico publicado en 1992

Life with home mechanical ventilation for young men with Duchenne muscular dystrophy

artículo científico publicado en 2010

Living with severe physical impairment, Duchenne's muscular dystrophy and home mechanical ventilation

artículo científico publicado en 2010

Physical capacity in non-ambulatory people with Duchenne muscular dystrophy or spinal muscular atrophy: a longitudinal study

artículo científico publicado en 2002

Physical characteristics and applicability of standard assessment methods in a total population of spinal muscular atrophy type II patients

scientific article published on 06 December 2009

Rasch analysis of clinical outcome measures in spinal muscular atrophy.

artículo científico publicado en 2013

The Duchenne muscular dystrophy population in Denmark, 1977-2001: prevalence, incidence and survival in relation to the introduction of ventilator use.

artículo científico publicado en 2003

Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)

Translation and validation of the Egen Klassifikation scale for the Spanish population: functional assessment for non-ambulatory individuals with Duchenne's muscular dystrophy and spinal muscular atrophy

artículo científico publicado el 1 de junio de 2013

Validity of the EK scale: a functional assessment of non-ambulatory individuals with Duchenne muscular dystrophy or spinal muscular atrophy

artículo científico publicado en 2001

[Evolution of functional capacity, assessed with the Egen Klassifikation scale, in the Spanish population with spinal muscular atrophy or Duchenne muscular dystrophy. A three year longitudinal study]

artículo científico publicado en 2015

[Indicators for an impending need of artificial respiration in patients with muscular dystrophy]

artículo científico publicado en 1993

[Life quality of patients with muscular failure, using permanent respiratory support, seen from their point of view. 2. Practical requirements and problems connected with respirator treatment]

artículo científico publicado en 1992

[Muscular dystrophy and exercise]

artículo científico publicado en 1989

Lista de obras de Birgit F Steffensen

206th ENMC International Workshop: Care for a novel group of patients - adults with Duchenne muscular dystrophy Naarden, The Netherlands, 23-25 May 2014.

A randomized comparative study of two methods for controlling Tendo Achilles contracture in Duchenne muscular dystrophy.

Adult life with Duchenne muscular dystrophy: observations among an emerging and unforeseen patient population.

Change in muscle strength over time in spinal muscular atrophy types II and III. A long-term follow-up study.

Developing and maintaining of user-defined personal competencies among young adults with congenital physical disability

Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale.

Fracture risk in patients with muscular dystrophy and spinal muscular atrophy

Functional assessment for people unable to walk due to spinal muscular atrophy and Duchenne muscular dystrophy. Translation and validation of the Egen Klassifikation 2 scale for the Spanish population

Indicators of need for mechanical ventilation in Duchenne muscular dystrophy and spinal muscular atrophy

Life quality of patients with muscular failure, using permanent respiratory support, seen from their point of view. 1. Information, choice and quality of life

Life with home mechanical ventilation for young men with Duchenne muscular dystrophy

Living with severe physical impairment, Duchenne's muscular dystrophy and home mechanical ventilation

Physical capacity in non-ambulatory people with Duchenne muscular dystrophy or spinal muscular atrophy: a longitudinal study

Physical characteristics and applicability of standard assessment methods in a total population of spinal muscular atrophy type II patients

Rasch analysis of clinical outcome measures in spinal muscular atrophy.

The Duchenne muscular dystrophy population in Denmark, 1977-2001: prevalence, incidence and survival in relation to the introduction of ventilator use.

Transition from childhood to adulthood in Duchenne muscular dystrophy (DMD)

Translation and validation of the Egen Klassifikation scale for the Spanish population: functional assessment for non-ambulatory individuals with Duchenne's muscular dystrophy and spinal muscular atrophy

Validity of the EK scale: a functional assessment of non-ambulatory individuals with Duchenne muscular dystrophy or spinal muscular atrophy

[Evolution of functional capacity, assessed with the Egen Klassifikation scale, in the Spanish population with spinal muscular atrophy or Duchenne muscular dystrophy. A three year longitudinal study]

[Indicators for an impending need of artificial respiration in patients with muscular dystrophy]

[Life quality of patients with muscular failure, using permanent respiratory support, seen from their point of view. 2. Practical requirements and problems connected with respirator treatment]

[Muscular dystrophy and exercise]