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Faculty Opinions recommendation of Cardiac defects contribute to the pathology of spinal muscular atrophy models.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.718864639.793502432
◽
2014
◽
Author(s):
Chris Henderson
Keyword(s):
Spinal Muscular Atrophy
◽
Muscular Atrophy
◽
Cardiac Defects
Download Full-text
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Cardiac defects contribute to the pathology of spinal muscular atrophy models
Human Molecular Genetics
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Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice
Human Molecular Genetics
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2010
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pp. 3906-3918
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Cited By ~ 119
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Muscular Atrophy
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Cardiac Defects
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Faculty Opinions recommendation of Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
◽
10.3410/f.718864641.793502433
◽
2014
◽
Author(s):
Chris Henderson
Keyword(s):
Spinal Muscular Atrophy
◽
Muscular Atrophy
◽
Cardiac Defects
Download Full-text
Development of an interest in spinal muscular atrophy and disabilities
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Gene Discovery Opens Door to Further Research in Inherited Neurological Disorders: Charcot-Marie-Tooth and Distal Spinal Muscular Atrophy Gene May Shed Light on Carpal Tunnel Syndrome and Lou Gehrig's Disease
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10.1037/e622342007-001
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Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
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Author(s):
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M Breiting
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A Müller
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...
Keyword(s):
Palliative Care
◽
Duchenne Muscular Dystrophy
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Muscular Dystrophy
◽
Spinal Muscular Atrophy
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Muscular Atrophy
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Neuromuscular Disorders
◽
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◽
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◽
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◽
Life Threatening
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Case Report: Respiratory management of a successful pregnancy in type II spinal muscular atrophy
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pp. S99-S99
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M Valter
◽
K Frank
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Case Report
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Spinal Muscular Atrophy
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Muscular Atrophy
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FV 953. Parents’ Experiences during the Compassionate Use Program (Nusinersen) for Patients with Spinal Muscular Atrophy Type 1—A Qualitative Interview Study
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2018
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Author(s):
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Astrid Pechmann
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Janbernd Kirschner
Keyword(s):
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Muscular Atrophy
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Interview Study
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Compassionate Use
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Spinal Muscular Atrophy Type
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Qualitative Interview Study
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Parents Experiences
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