MRI findings in an atypical case of Kearns-Sayre syndrome: a case report

A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai · Nature · 1990 · 2.1K citations

Biology, Mitochondrial Function, Genetic Disorder +6

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

Carlos T. Moraes, Salvatore DiMauro, Massimo Zeviani et al. · New England Journal of Medicine · 1989 · 1K citations

Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block

Thomas P. Kearns · A M A Archives of Ophthalmology · 1958 · 623 citations

Ocular Disease, Pathology, Diabetic Retinopathy +17

A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1991 · 327 citations

Mitochondrial Myopathy, Lactic Acidosis, Mendelian Disorder +9

Neuroradiologic findings in children with mitochondrial disorders.

Leena Valanne, Leena Ketonen, Anna Majander et al. · PubMed · 1998 · 196 citations · Full text