A. Mathew

Limb girdle muscular dystrophy due to LAMA2 mutations: Diagnostic difficulties due to associated peripheral neuropathy

F. Muntoni, C. Sewry, A. Foley, 2014, Neuromuscular Disorders.

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

S. Züchner, M. Lek, F. Muntoni, 2013, Brain : a journal of neurology.

Sporadic Hemiplegic Migraine with CACNA1A Mutation Masquerading as Acute Meningoencephalitis

A. A. Mathew, Siddhartha Gajam, R. Peterson, 2022, Annals of Indian Academy of Neurology.

Cardiomyopathy in Duchenne Muscular Dystrophy

Ramya Ramesh, Madhuri Maganthi, Saravanan Palaniappan, 2022, JACC: Asia.

SEPN1-Related Myopathy: The Importance of Diagnosis and Challenges to Management of CMD in Resource Poor Settings

S. Rath, Madhuri Maganthi, Siddhartha Gajam, 2021, Annals of Indian Academy of Neurology.