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Neuromuscular Disorders : NMD
|
September 9, 2009
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations
James Collins, Kevin E Bove, David Dimmock, et al.
Neuromuscular Disorders : NMD
|
September 11, 2016
Diagnosis and treatment of obsessive compulsive behavior in a boy with Duchenne muscular dystrophy and autism spectrum disorder: A case report
Jos G M Hendriksen, Sylvia Klinkenberg, Phillipe Collin, et al.
Radiology
|
May 27, 2010
T2 mapping in Duchenne muscular dystrophy: distribution of disease activity and correlation with clinical assessments
Hee Kyung Kim, Tal Laor, Paul S Horn, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 18, 2004
Measurement of reduced and oxidized coenzyme Q9 and coenzyme Q10 levels in mouse tissues by HPLC with coulometric detection
Peter H Tang, Michael V Miles, Lili Miles, et al.
Neuromuscular Disorders : NMD
|
December 21, 2011
Multiple exon skipping strategies to by-pass dystrophin mutations
Carl F Adkin, Penelope L Meloni, Susan Fletcher, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 17, 2022
<i>Tm4sf1</i>-marked Endothelial Subpopulation Is Dysregulated in Pulmonary Arterial Hypertension
Jason Hong, Brenda Wong, Caroline Huynh, et al.
Pediatrics
|
November 7, 2012
Health-related quality of life in children and adolescents with Duchenne muscular dystrophy
Karen Uzark, Eileen King, Linda Cripe, et al.
Annals of Clinical and Translational Neurology
|
August 22, 2018
Placebo-controlled Phase 2 Trial of Drisapersen for Duchenne Muscular Dystrophy
Craig M McDonald, Brenda Wong, Kevin M Flanigan, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
MicroRNA and mRNA Expression Changes in Steroid Naïve and Steroid Treated DMD Patients
Da Zhi Liu, Boryana Stamova, Shengyong Hu, et al.
Human Mutation
|
March 17, 2006
Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome
Leomar Y Ballester, D Woodrow Benson, Brenda Wong, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 6
Neuromuscular Disorders : NMD
|
September 9, 2009
Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations
James Collins, Kevin E Bove, David Dimmock, et al.
Neuromuscular Disorders : NMD
|
September 11, 2016
Diagnosis and treatment of obsessive compulsive behavior in a boy with Duchenne muscular dystrophy and autism spectrum disorder: A case report
Jos G M Hendriksen, Sylvia Klinkenberg, Phillipe Collin, et al.
Radiology
|
May 27, 2010
T2 mapping in Duchenne muscular dystrophy: distribution of disease activity and correlation with clinical assessments
Hee Kyung Kim, Tal Laor, Paul S Horn, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 18, 2004
Measurement of reduced and oxidized coenzyme Q9 and coenzyme Q10 levels in mouse tissues by HPLC with coulometric detection
Peter H Tang, Michael V Miles, Lili Miles, et al.
Neuromuscular Disorders : NMD
|
December 21, 2011
Multiple exon skipping strategies to by-pass dystrophin mutations
Carl F Adkin, Penelope L Meloni, Susan Fletcher, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 17, 2022
<i>Tm4sf1</i>-marked Endothelial Subpopulation Is Dysregulated in Pulmonary Arterial Hypertension
Jason Hong, Brenda Wong, Caroline Huynh, et al.
Pediatrics
|
November 7, 2012
Health-related quality of life in children and adolescents with Duchenne muscular dystrophy
Karen Uzark, Eileen King, Linda Cripe, et al.
Annals of Clinical and Translational Neurology
|
August 22, 2018
Placebo-controlled Phase 2 Trial of Drisapersen for Duchenne Muscular Dystrophy
Craig M McDonald, Brenda Wong, Kevin M Flanigan, et al.
Journal of Neuromuscular Diseases
|
November 19, 2016
MicroRNA and mRNA Expression Changes in Steroid Naïve and Steroid Treated DMD Patients
Da Zhi Liu, Boryana Stamova, Shengyong Hu, et al.
Human Mutation
|
March 17, 2006
Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome
Leomar Y Ballester, D Woodrow Benson, Brenda Wong, et al.
Page
of 6