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Journal of Neurology
|
October 27, 2004
Myotonic dystrophy type 2 and related myotonic disorders
Giovanni Meola, Richard T Moxley
Current Treatment Options in Neurology
|
March 13, 2008
Treatment options for Duchenne muscular dystrophy
Emma Ciafaloni, Richard T Moxley
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
March 31, 2007
The nondystrophic myotonias
Chad R Heatwole, Richard T Moxley
Neurology
|
February 3, 2016
Practice guideline update summary: Corticosteroid treatment of Duchenne muscular dystrophy [RETIRED]: Report of the Guideline Development Subcommittee of the American Academy of Neurology
David Gloss, Richard T Moxley, Stephen Ashwal, et al.
Neuromuscular Disorders : NMD
|
August 29, 2009
Scaled-down genetic analysis of myotonic dystrophy type 1 and type 2
Masayuki Nakamori, Krzysztof Sobczak, Richard T Moxley, et al.
Archives of Neurology
|
August 16, 2006
Laboratory abnormalities in ambulatory patients with myotonic dystrophy type 1
Chad R Heatwole, Jill Miller, Bill Martens, et al.
Journal of Child Neurology
|
June 29, 2010
Change in natural history of Duchenne muscular dystrophy with long-term corticosteroid treatment: implications for management
Richard T Moxley, Shree Pandya, Emma Ciafaloni, et al.
Muscle & Nerve
|
June 26, 2007
Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1)
Richard T Moxley, Eric L Logigian, William B Martens, et al.
Human Molecular Genetics
|
October 22, 2004
Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons
Hong Jiang, Ami Mankodi, Maurice S Swanson, et al.
Journal of the American Academy of Dermatology
|
July 26, 2002
Thalidomide therapy for cicatricial pemphigoid
Daihung Jay Duong, Richard T Moxley, Robert M Kellman, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Journal of Neurology
|
October 27, 2004
Myotonic dystrophy type 2 and related myotonic disorders
Giovanni Meola, Richard T Moxley
Current Treatment Options in Neurology
|
March 13, 2008
Treatment options for Duchenne muscular dystrophy
Emma Ciafaloni, Richard T Moxley
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
March 31, 2007
The nondystrophic myotonias
Chad R Heatwole, Richard T Moxley
Neurology
|
February 3, 2016
Practice guideline update summary: Corticosteroid treatment of Duchenne muscular dystrophy [RETIRED]: Report of the Guideline Development Subcommittee of the American Academy of Neurology
David Gloss, Richard T Moxley, Stephen Ashwal, et al.
Neuromuscular Disorders : NMD
|
August 29, 2009
Scaled-down genetic analysis of myotonic dystrophy type 1 and type 2
Masayuki Nakamori, Krzysztof Sobczak, Richard T Moxley, et al.
Archives of Neurology
|
August 16, 2006
Laboratory abnormalities in ambulatory patients with myotonic dystrophy type 1
Chad R Heatwole, Jill Miller, Bill Martens, et al.
Journal of Child Neurology
|
June 29, 2010
Change in natural history of Duchenne muscular dystrophy with long-term corticosteroid treatment: implications for management
Richard T Moxley, Shree Pandya, Emma Ciafaloni, et al.
Muscle & Nerve
|
June 26, 2007
Computerized hand grip myometry reliably measures myotonia and muscle strength in myotonic dystrophy (DM1)
Richard T Moxley, Eric L Logigian, William B Martens, et al.
Human Molecular Genetics
|
October 22, 2004
Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons
Hong Jiang, Ami Mankodi, Maurice S Swanson, et al.
Journal of the American Academy of Dermatology
|
July 26, 2002
Thalidomide therapy for cicatricial pemphigoid
Daihung Jay Duong, Richard T Moxley, Robert M Kellman, et al.
Page
of 5