Lista de obras - Laura E. Case - Dominio Público Uruguay

Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe disease

artículo científico publicado en 2014

Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa

artículo científico publicado en 2012

Correlation between quantitative whole-body muscle magnetic resonance imaging and clinical muscle weakness in pompe disease

artículo científico publicado en 2015

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

artículo científico publicado en 2009

Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

artículo científico publicado en 2009

Early cognitive development in children with infantile Pompe disease

artículo científico publicado en 2011

Effects of respiratory muscle training (RMT) in children with infantile-onset Pompe disease and respiratory muscle weakness

artículo científico publicado en 2014

Erratum to “Pompe disease: Design, methodology, and early findings from the Pompe Registry” [Mol. Genet. Metabol. 103 (2011) 1–11]

scholarly article published in Molecular Genetics and Metabolism

Exercise and duchenne muscular dystrophy: Where we have been and where we need to go

scientific article published on 01 May 2012

Generating color-coded anatomic muscle maps for correlation of quantitative magnetic resonance imaging analysis with clinical examination in neuromuscular disorders

artículo científico publicado en 2013

Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study

scientific article published on 18 October 2008

Infantile Pompe disease on ERT: update on clinical presentation, musculoskeletal management, and exercise considerations.

artículo científico

Oropharyngeal dysphagia in infants and children with infantile Pompe disease.

artículo científico publicado en 2009

Pompe disease: Design, methodology, and early findings from the Pompe Registry

article by Barry J. Byrne et al published May 2011 in Molecular Genetics and Metabolism

Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease

artículo científico publicado en 2014

Small-fiber neuropathy in pompe disease: first reported cases and prospective screening of a clinic cohort.

artículo científico publicado en 2015

Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease.

artículo científico publicado en 2012

The Effects of Aerobic Exercise on Endurance, Strength, Function and Self-Perception in Adolescents with Spastic Cerebral Palsy: A Report of Three Case Studies

scientific article published on 01 January 2005

The Pompe Registry: Centralized Data Collection to Track the Natural Course of Pompe Disease

The emerging phenotype of long-term survivors with infantile Pompe disease.

artículo científico publicado en 2012

The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe Registry

artículo científico publicado en 2011

Lista de obras de Laura E. Case

Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe disease

Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa

Correlation between quantitative whole-body muscle magnetic resonance imaging and clinical muscle weakness in pompe disease

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care

Early cognitive development in children with infantile Pompe disease

Effects of respiratory muscle training (RMT) in children with infantile-onset Pompe disease and respiratory muscle weakness

Erratum to “Pompe disease: Design, methodology, and early findings from the Pompe Registry” [Mol. Genet. Metabol. 103 (2011) 1–11]

Exercise and duchenne muscular dystrophy: Where we have been and where we need to go

Generating color-coded anatomic muscle maps for correlation of quantitative magnetic resonance imaging analysis with clinical examination in neuromuscular disorders

Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study

Infantile Pompe disease on ERT: update on clinical presentation, musculoskeletal management, and exercise considerations.

Oropharyngeal dysphagia in infants and children with infantile Pompe disease.

Pompe disease: Design, methodology, and early findings from the Pompe Registry

Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease

Small-fiber neuropathy in pompe disease: first reported cases and prospective screening of a clinic cohort.

Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease.

The Effects of Aerobic Exercise on Endurance, Strength, Function and Self-Perception in Adolescents with Spastic Cerebral Palsy: A Report of Three Case Studies

The Pompe Registry: Centralized Data Collection to Track the Natural Course of Pompe Disease

The emerging phenotype of long-term survivors with infantile Pompe disease.

The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe Registry