K. Sivakumar

Glycolysis-enhancing α1-adrenergic antagonists modify cognitive symptoms related to Parkinson’s disease

N. Narayanan, Georgina M. Aldridge, J. Simmering, 2022, npj Parkinson's Disease.

Late‐onset muscle weakness in partial phosphofructokinase deficiency

M. Dalakas, K. Sivakumar, L. Goldfarb, 1996, Neurology.

Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease.

M. Dubnick, J. Nagle, M. Dalakas, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion body myopathy

J. Nagle, M. Dalakas, K. Sivakumar, 1995, Annals of neurology.

Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.

M. Dalakas, Kye-yoon Park, K. Sivakumar, 2000, The New England journal of medicine.

Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic origins

C. Toro, J. Bilbao, M. Dalakas, 2013, BMC Neurology.