Focal glomerulosclerosis expanding from the glomerular vascular pole in a Japanese male with mitochondrial-DNA mutation [2]

Nephrology Dialysis Transplantation

Volumn 17, Issue 1, 2002, Pages 172-174

  Segawa Takaeda, Chikako ^a   Takeda, Shin Ichi ^a   Ieki, Yasuhiko ^a   Takazakura, Eisuke ^a   Haratake, Joji ^a   Wada, Takashi ^b   Yokoyama, Hitoshi ^b  

^a Kurobe City Hospital   (Japan)

^b KANAZAWA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CREATININE; CYCLOSPORIN; IMMUNOGLOBULIN M; MITOCHONDRIAL DNA; PREDNISOLONE;

ADOLESCENT; CASE REPORT; DIABETES MELLITUS; DIABETIC KETOACIDOSIS; ELECTRON MICROSCOPY; FOCAL GLOMERULOSCLEROSIS; GENE MUTATION; HEMODIALYSIS; HUMAN; IMMUNOHISTOCHEMISTRY; JAPAN; KIDNEY BIOPSY; KIDNEY FAILURE; KIDNEY FUNCTION; LETTER; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEINURIA; TREATMENT FAILURE;

EID: 0036146155     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/17.1.172     Document Type: Letter

References (7)

1. Hereditary mitochondrial myopathy with lactic acidemia, a de-Toni-Debre-Fanconi syndrome and a defective respiratory chain in voluntary striated muscles
2. A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation
3. Focal segmental glomerulosclerosis associated with mitochondrial cytopathy
4. UUR) gene mutation
5. Mitochondrial encephalomyopathies preceded by de-Toni-Debre-Fanconi syndrome or focal segmental glomerulosclerosis
6. Focal segmental glomerular sclerosis in adults: Presentation, course and response to treatment
7. Pathogenesis and significance of nonprimary focal and segmental glomerulosclerosis