Lewis P. Rowland

Amyotrophic Lateral Sclerosis

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

Inclusion body myositis and myopathies

Deletions of mitochondrial DNA in Kearns‐Sayre syndrome

Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface

Peripheral Neuropathy

Hashimoto Encephalopathy

MELAS: Clinical features, biochemistry, and molecular genetics

MELAS: An original case and clinical criteria for diagnosis

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)

Myasthenic crisis