Sujatha Gurunathan

The key pathologic change of the muscular dystrophy is the myonecrosis. At an early phase, necrotic fibers appear swollen, homogeneous and deeply eosinophilic. This disease is caused by mutations of dystrophin, the largest known human gene, located on chromosome Xq21.
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Simply Stated: Updates in LAMA2 Muscular Dystrophy

By Sujatha Gurunathan | February 20, 2024
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Research Study Alert: Genome-Wide Association Study in People with MuSK MG

By Sujatha Gurunathan | February 5, 2024
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Research Study Alert: Noninterventional Study in People with DMD and BMD

By Sujatha Gurunathan | January 11, 2024
Color image of a real life young physically impaired ALS patient computer gaming with the help of his electronic wheelchair.
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Simply Stated: Updates in Collagen VI-Related Dystrophy

By Sujatha Gurunathan | January 6, 2024
Mitochondrion in cell cross section
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Simply Stated: Research Updates in Leigh Syndrome

By Sujatha Gurunathan | December 6, 2023
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Clinical Trial Alert: Phase 3 Study of Brepocitinib in Adults with Dermatomyositis

By Sujatha Gurunathan | November 16, 2023
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Clinical Trial Alert: Phase 3 Study of Batoclimab in Adults with MG

By Sujatha Gurunathan | September 29, 2023
Young disabled man in wheelchair doing strength exercises for hands in the rehabilitation clinic. Doctor physiotherapist helping him
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Simply Stated: Research Updates in Periodic Paralysis

By Sujatha Gurunathan | September 25, 2023
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Research Study Alert: Observational Study of Cardiovascular Function in Children with BMD or DMD

By Sujatha Gurunathan | September 22, 2023
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Deconstructing SMA Types and Treatments

By Sujatha Gurunathan | August 23, 2023