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Journal of Clinical Neuromuscular Disease
|
November 16, 2018
Toxic Myopathy due to Antidopaminergic Medication Without Neuroleptic Malignant Syndrome
Yohei Harada, Tuhin Virmani, Murat Gokden, et al.
Journal of Clinical Neuromuscular Disease
|
May 27, 2020
Pseudometabolic Presentation of Dystrophinopathy in a Family Due to a Rare Nonsense Mutation
Ezgi Saylam, Akilandeswari Aravindhan, Vikki Stefans, et al.
Journal of Clinical Neuromuscular Disease
|
May 27, 2020
BAG3 Myopathy Presenting With Prominent Neuropathic Phenotype and No Cardiac or Respiratory Involvement: A Case Report and Literature Review
Lindsay Malatesta, Kapil Arya, Murat Gokden, et al.
Muscle & Nerve
|
February 21, 2026
Pathologic Variability Associated With Phenotypic Differences in Siblings With ACTA1 Myopathy
Robert Kiss, Steven A Moore, Vikki Stefans, et al.
Neurology
|
September 12, 2020
Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching
Hannah Smashey Lewis, Balaji Subramanian Srinivasa Sekaran, Vikki Stefans, et al.
Child Neurology Open
|
May 13, 2022
Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in <i>FKRP</i> Gene
Erin Willis, Steven A Moore, Mary O Cox, et al.
Archives of Physical Medicine and Rehabilitation
|
January 11, 2005
Experiences from the development of a comprehensive family support program for pediatric trauma and rehabilitation patients
Mary E Aitken, Patricia Korehbandi, Donna Parnell, et al.
Neurology. Genetics
|
February 12, 2020
A novel noncoding <i>FKRP</i> mutation in early onset limb-girdle muscular dystrophy
Ezgi Saylam, Steven A Moore, Akilandeswari Aravindhan, et al.
American Journal of Medical Genetics. Part A
|
April 4, 2019
Constitutive activation of the PI3K-AKT pathway and cardiovascular abnormalities in an individual with Kosaki overgrowth syndrome
Yuri A Zarate, Luigi Boccuto, Sujata Srikanth, et al.
Muscle & Nerve
|
July 26, 2020
Combination molecular therapies for type 1 spinal muscular atrophy
Yohei Harada, Vamshi K Rao, Kapil Arya, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Journal of Clinical Neuromuscular Disease
|
November 16, 2018
Toxic Myopathy due to Antidopaminergic Medication Without Neuroleptic Malignant Syndrome
Yohei Harada, Tuhin Virmani, Murat Gokden, et al.
Journal of Clinical Neuromuscular Disease
|
May 27, 2020
Pseudometabolic Presentation of Dystrophinopathy in a Family Due to a Rare Nonsense Mutation
Ezgi Saylam, Akilandeswari Aravindhan, Vikki Stefans, et al.
Journal of Clinical Neuromuscular Disease
|
May 27, 2020
BAG3 Myopathy Presenting With Prominent Neuropathic Phenotype and No Cardiac or Respiratory Involvement: A Case Report and Literature Review
Lindsay Malatesta, Kapil Arya, Murat Gokden, et al.
Muscle & Nerve
|
February 21, 2026
Pathologic Variability Associated With Phenotypic Differences in Siblings With ACTA1 Myopathy
Robert Kiss, Steven A Moore, Vikki Stefans, et al.
Neurology
|
September 12, 2020
Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching
Hannah Smashey Lewis, Balaji Subramanian Srinivasa Sekaran, Vikki Stefans, et al.
Child Neurology Open
|
May 13, 2022
Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in <i>FKRP</i> Gene
Erin Willis, Steven A Moore, Mary O Cox, et al.
Archives of Physical Medicine and Rehabilitation
|
January 11, 2005
Experiences from the development of a comprehensive family support program for pediatric trauma and rehabilitation patients
Mary E Aitken, Patricia Korehbandi, Donna Parnell, et al.
Neurology. Genetics
|
February 12, 2020
A novel noncoding <i>FKRP</i> mutation in early onset limb-girdle muscular dystrophy
Ezgi Saylam, Steven A Moore, Akilandeswari Aravindhan, et al.
American Journal of Medical Genetics. Part A
|
April 4, 2019
Constitutive activation of the PI3K-AKT pathway and cardiovascular abnormalities in an individual with Kosaki overgrowth syndrome
Yuri A Zarate, Luigi Boccuto, Sujata Srikanth, et al.
Muscle & Nerve
|
July 26, 2020
Combination molecular therapies for type 1 spinal muscular atrophy
Yohei Harada, Vamshi K Rao, Kapil Arya, et al.
Page
of 2