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Seminars in Pediatric Neurology
|
November 1, 2011
Child neurology residency training in neuromuscular disorders
Basil T Darras
Neurology
|
February 11, 2012
More can be less: SMN1 gene duplications are associated with sporadic ALS
Basil T Darras
Neurology
|
July 1, 2011
Non-5q spinal muscular atrophies: the alphanumeric soup thickens
Basil T Darras
Pediatric Clinics of North America
|
May 30, 2015
Spinal muscular atrophies
Basil T Darras
Neurology
|
November 28, 2014
Congenital myopathies: Rebuilding the natural history, one gene at a time
Enrico Bertini, Basil T Darras
Neurology
|
September 18, 2013
Predicting hearing loss in facioscapulohumeral muscular dystrophy
Basil T Darras, Rabi Tawil
Pediatric Neurology
|
August 1, 2006
Catecholamine toxicity in aromatic L-amino acid decarboxylase deficiency
Irina A Anselm, Basil T Darras
Neurology
|
January 4, 2013
Making sense of genetic heterogeneity: Emergence of pathways in developmental brain disorders
Alex R Paciorkowski, Basil T Darras
Current Opinion in Pediatrics
|
November 19, 2013
Neuromuscular disorders: from diagnosis to translational research, drug development and clinical trials
Robert C Tasker, Basil T Darras
Neurology
|
August 27, 2017
X-linked myotubular myopathy: Living longer and awaiting treatment
Richard S Finkel, Basil T Darras
Page
of 23
Search research articles
Search
Showing results (1-10 of 222) with videos related to
Sort By:
Page
of 23
Seminars in Pediatric Neurology
|
November 1, 2011
Child neurology residency training in neuromuscular disorders
Basil T Darras
Neurology
|
February 11, 2012
More can be less: SMN1 gene duplications are associated with sporadic ALS
Basil T Darras
Neurology
|
July 1, 2011
Non-5q spinal muscular atrophies: the alphanumeric soup thickens
Basil T Darras
Pediatric Clinics of North America
|
May 30, 2015
Spinal muscular atrophies
Basil T Darras
Neurology
|
November 28, 2014
Congenital myopathies: Rebuilding the natural history, one gene at a time
Enrico Bertini, Basil T Darras
Neurology
|
September 18, 2013
Predicting hearing loss in facioscapulohumeral muscular dystrophy
Basil T Darras, Rabi Tawil
Pediatric Neurology
|
August 1, 2006
Catecholamine toxicity in aromatic L-amino acid decarboxylase deficiency
Irina A Anselm, Basil T Darras
Neurology
|
January 4, 2013
Making sense of genetic heterogeneity: Emergence of pathways in developmental brain disorders
Alex R Paciorkowski, Basil T Darras
Current Opinion in Pediatrics
|
November 19, 2013
Neuromuscular disorders: from diagnosis to translational research, drug development and clinical trials
Robert C Tasker, Basil T Darras
Neurology
|
August 27, 2017
X-linked myotubular myopathy: Living longer and awaiting treatment
Richard S Finkel, Basil T Darras
Page
of 23