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Pediatrics
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October 3, 2018
Rehabilitation Management of the Patient With Duchenne Muscular Dystrophy
Laura E Case, Susan D Apkon, Michelle Eagle, et al.
Molecular Genetics and Metabolism
|
September 21, 2011
The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe Registry
Mark Roberts, Priya S Kishnani, Ans T van der Ploeg, et al.
Molecular Genetics and Metabolism
|
October 15, 2021
Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literature
Anna Paschall, Aleena A Khan, Syed Faaiz Enam, et al.
Molecular Genetics and Metabolism
|
July 9, 2016
Physical therapy management of infants and children with hypophosphatasia
Dawn Phillips, Laura E Case, Donna Griffin, et al.
Pediatrics
|
October 3, 2018
A Transition Toolkit for Duchenne Muscular Dystrophy
Christina J Trout, Laura E Case, Paula R Clemens, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 21, 2014
Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe disease
Dwight D Koeberl, Stephanie Austin, Laura E Case, et al.
Stem Cells Translational Medicine
|
June 4, 2021
Sibling umbilical cord blood infusion is safe in young children with cerebral palsy
Jessica M Sun, Laura E Case, Mohamad A Mikati, et al.
Developmental Medicine and Child Neurology
|
July 11, 2022
Motor function and safety after allogeneic cord blood and cord tissue-derived mesenchymal stromal cells in cerebral palsy: An open-label, randomized trial
Jessica M Sun, Laura E Case, Colleen McLaughlin, et al.
Molecular Genetics and Metabolism
|
October 16, 2012
Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa
Jeffrey J Horvath, Stephanie L Austin, Harrison N Jones, et al.
Molecular Genetics and Metabolism
|
September 27, 2025
Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe disease
Neelam Makhijani, Myriam Boueri, Bijan Abar, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 57) with videos related to
Sort By:
Page
of 6
Pediatrics
|
October 3, 2018
Rehabilitation Management of the Patient With Duchenne Muscular Dystrophy
Laura E Case, Susan D Apkon, Michelle Eagle, et al.
Molecular Genetics and Metabolism
|
September 21, 2011
The prevalence and impact of scoliosis in Pompe disease: lessons learned from the Pompe Registry
Mark Roberts, Priya S Kishnani, Ans T van der Ploeg, et al.
Molecular Genetics and Metabolism
|
October 15, 2021
Physical therapy assessment and whole-body magnetic resonance imaging findings in children with glycogen storage disease type IIIa: A clinical study and review of the literature
Anna Paschall, Aleena A Khan, Syed Faaiz Enam, et al.
Molecular Genetics and Metabolism
|
July 9, 2016
Physical therapy management of infants and children with hypophosphatasia
Dawn Phillips, Laura E Case, Donna Griffin, et al.
Pediatrics
|
October 3, 2018
A Transition Toolkit for Duchenne Muscular Dystrophy
Christina J Trout, Laura E Case, Paula R Clemens, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
January 21, 2014
Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe disease
Dwight D Koeberl, Stephanie Austin, Laura E Case, et al.
Stem Cells Translational Medicine
|
June 4, 2021
Sibling umbilical cord blood infusion is safe in young children with cerebral palsy
Jessica M Sun, Laura E Case, Mohamad A Mikati, et al.
Developmental Medicine and Child Neurology
|
July 11, 2022
Motor function and safety after allogeneic cord blood and cord tissue-derived mesenchymal stromal cells in cerebral palsy: An open-label, randomized trial
Jessica M Sun, Laura E Case, Colleen McLaughlin, et al.
Molecular Genetics and Metabolism
|
October 16, 2012
Bulbar muscle weakness and fatty lingual infiltration in glycogen storage disorder type IIIa
Jeffrey J Horvath, Stephanie L Austin, Harrison N Jones, et al.
Molecular Genetics and Metabolism
|
September 27, 2025
Quantitative muscle ultrasound as a window into disease progression in infantile-onset Pompe disease
Neelam Makhijani, Myriam Boueri, Bijan Abar, et al.
Page
of 6