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Seminars in Pediatric Neurology
|
June 6, 2003
Hereditary causes of chorea in childhood
Katherine D Mathews
Neurologic Clinics
|
January 28, 2004
Muscular dystrophy overview: genetics and diagnosis
Katherine D Mathews
Archives of Neurology
|
January 21, 2004
Multiminicore myopathy, central core disease, malignant hyperthermia susceptibility, and RYR1 mutations: one disease with many faces?
Katherine D Mathews, Steven A Moore
Current Neurology and Neuroscience Reports
|
January 1, 2003
Limb-girdle muscular dystrophy
Katherine D Mathews, Steven A Moore
Muscle & Nerve
|
October 29, 2020
Combination molecular therapies for spinal muscular atrophy: How much is enough?
Katherine D Mathews, Susan T Iannaccone
JBJS Case Connector
|
March 16, 2022
Effect of Denosumab on Bone Health in Adult Patients with Duchenne/Becker Muscular Dystrophy: A Report of 2 Cases
Chermaine Hung, Katherine D Mathews, Amal Shibli-Rahhal
Clinical Pediatrics
|
September 13, 2013
A 16-week-old infant with failure to thrive and hypotonia
Benton Ng, Katherine D Mathews, Heather L Bartlett
Muscle & Nerve
|
January 25, 2018
Dystrophinopathy muscle biopsies in the genetic testing ERA: One center's data
Courtney R Carlson, Steven A Moore, Katherine D Mathews
Journal of Child Neurology
|
December 1, 2021
Central Nervous System Infections Due to <i>Streptococcus anginosus</i> Group: A Single-Center Case Series
Sujana Madathil, Satsuki Matsumoto, Katherine D Mathews, et al.
Muscle & Nerve
|
January 13, 2019
Use of bone age for evaluating bone density in patients with Duchenne muscular dystrophy: A preliminary report
Asma Al-Zougbi, Katherine D Mathews, Amal Shibli-Rahhal
Page
of 13
Search research articles
Search
Showing results (1-10 of 125) with videos related to
Sort By:
Page
of 13
Seminars in Pediatric Neurology
|
June 6, 2003
Hereditary causes of chorea in childhood
Katherine D Mathews
Neurologic Clinics
|
January 28, 2004
Muscular dystrophy overview: genetics and diagnosis
Katherine D Mathews
Archives of Neurology
|
January 21, 2004
Multiminicore myopathy, central core disease, malignant hyperthermia susceptibility, and RYR1 mutations: one disease with many faces?
Katherine D Mathews, Steven A Moore
Current Neurology and Neuroscience Reports
|
January 1, 2003
Limb-girdle muscular dystrophy
Katherine D Mathews, Steven A Moore
Muscle & Nerve
|
October 29, 2020
Combination molecular therapies for spinal muscular atrophy: How much is enough?
Katherine D Mathews, Susan T Iannaccone
JBJS Case Connector
|
March 16, 2022
Effect of Denosumab on Bone Health in Adult Patients with Duchenne/Becker Muscular Dystrophy: A Report of 2 Cases
Chermaine Hung, Katherine D Mathews, Amal Shibli-Rahhal
Clinical Pediatrics
|
September 13, 2013
A 16-week-old infant with failure to thrive and hypotonia
Benton Ng, Katherine D Mathews, Heather L Bartlett
Muscle & Nerve
|
January 25, 2018
Dystrophinopathy muscle biopsies in the genetic testing ERA: One center's data
Courtney R Carlson, Steven A Moore, Katherine D Mathews
Journal of Child Neurology
|
December 1, 2021
Central Nervous System Infections Due to <i>Streptococcus anginosus</i> Group: A Single-Center Case Series
Sujana Madathil, Satsuki Matsumoto, Katherine D Mathews, et al.
Muscle & Nerve
|
January 13, 2019
Use of bone age for evaluating bone density in patients with Duchenne muscular dystrophy: A preliminary report
Asma Al-Zougbi, Katherine D Mathews, Amal Shibli-Rahhal
Page
of 13