Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes syndrome with hypothyroidism and focal segmental glomerulosclerosis in a paediatric patient

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

Life Sciences, Genetics, Molecular Genetics +11

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

Simon Hammans, M G Sweeney, Martin Brockington et al. · The Lancet · 1991 · 182 citations

Life Sciences, Genetics, Molecular Genetics +16

Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation

Osamu Hotta, Chiyoko N. Inoue, Shigeaki Miyabayashi et al. · Kidney International · 2001 · 154 citations · Full text

Medicine, Genetics, Pathology +16

Mechanical stretch induces podocyte hypertrophy in vitro1

Arndt T. Petermann, Jeffrey W. Pippin, Raghu Durvasula et al. · Kidney International · 2004 · 104 citations · Full text

Natural Sciences, Cell Biology, Physiology +12

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

Masashi Tanaka, Hidekazu Ino, Kinji Ohno et al. · Biochemical and Biophysical Research Communications · 1991 · 86 citations

Life Sciences, Genetics, Molecular Genetics +17