159 related articles for article (PubMed ID: 35246049)
1. A case report of mitochondrial myopathy with membranous nephropathy.
Cai M; Yu Q; Bao J
BMC Nephrol; 2022 Mar; 23(1):87. PubMed ID: 35246049
[TBL] [Abstract][Full Text] [Related]
2. Renal Involvement in Neuropathy, Ataxia, Retinitis Pigmentosa (NARP) Syndrome: A Case Report.
Lemoine S; Panaye M; Rabeyrin M; Errazuriz-Cerda E; Mousson de Camaret B; Petiot P; Juillard L; Guebre-Egziabher F
Am J Kidney Dis; 2018 May; 71(5):754-757. PubMed ID: 29224958
[TBL] [Abstract][Full Text] [Related]
3. Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutations.
Tosserams A; Papadopoulos C; Jardel C; Lemière I; Romero NB; De Lonlay P; Wahbi K; Voermans N; Hogrel JY; Laforêt P
Mitochondrion; 2018 Mar; 39():26-29. PubMed ID: 28823815
[TBL] [Abstract][Full Text] [Related]
4. Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.
Hotta O; Inoue CN; Miyabayashi S; Furuta T; Takeuchi A; Taguma Y
Kidney Int; 2001 Apr; 59(4):1236-43. PubMed ID: 11260383
[TBL] [Abstract][Full Text] [Related]
5. [Membranous nephropathy - the most commonly diagnosed glomerulopathy in patients who underwent renal biopsy in the Department of Internal Medicine, Nephrology and Endocrinology St. Queen Jadwiga Clinical District Hospital No. 2 in Rzeszow].
Kołodziej-Kłęk A; Gala-Błądzińska A; Okoń K; Sadowska A; Świder G
Przegl Lek; 2017; 74(2):76-80. PubMed ID: 29694762
[TBL] [Abstract][Full Text] [Related]
6. Posttransplant de novo membranous nephropathy in childhood.
Sebire NJ; Bockenhauer D
Fetal Pediatr Pathol; 2005; 24(2):95-103. PubMed ID: 16243754
[TBL] [Abstract][Full Text] [Related]
7. An 80-year-old mitochondrial disease patient with A3243G tRNA(Leu(UUR)) gene presenting cardiac dysfunction as the main symptom.
Higashikata T; Koyama J; Shimada H; Yazaki M; Owa M; Ikeda S
Intern Med; 2001 May; 40(5):405-8. PubMed ID: 11393411
[TBL] [Abstract][Full Text] [Related]
8. Focal segmental glomerulosclerosis is not a sufficient predictor of renal outcome in patients with membranous nephropathy.
Heeringa SF; Branten AJ; Deegens JK; Steenbergen E; Wetzels JF
Nephrol Dial Transplant; 2007 Aug; 22(8):2201-7. PubMed ID: 17442739
[TBL] [Abstract][Full Text] [Related]
9. Renal function and mitochondrial cytopathy (MC): more questions than answers?
Hall AM; Unwin RJ; Hanna MG; Duchen MR
QJM; 2008 Oct; 101(10):755-66. PubMed ID: 18487272
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial myopathy with predominant respiratory dysfunction in a patient with A3243G mutation in the mitochondrial tRNA(Leu(UUR))gene.
Yang CC; Hwang CC; Pang CY; Wei YH
J Formos Med Assoc; 1998 Oct; 97(10):715-9. PubMed ID: 9830283
[TBL] [Abstract][Full Text] [Related]
11. Focal Segmental Glomerulosclerosis Associated with Chronic Progressive External Ophthalmoplegia and Mitochondrial DNA A3243G Mutation.
Narumi K; Mishima E; Akiyama Y; Matsuhashi T; Nakamichi T; Kisu K; Nishiyama S; Ikenouchi H; Kikuchi A; Izumi R; Miyazaki M; Abe T; Sato H; Ito S
Nephron; 2018; 138(3):243-248. PubMed ID: 29190634
[TBL] [Abstract][Full Text] [Related]
12. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
Zhang XA; Wu HC; Zhang BF; Yu W; Fan QS
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):18-21. PubMed ID: 15696472
[TBL] [Abstract][Full Text] [Related]
13. Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature review.
Damore ME; Speiser PW; Slonim AE; New MI; Shanske S; Xia W; Santorelli FM; DiMauro S
J Pediatr Endocrinol Metab; 1999; 12(2):207-13. PubMed ID: 10392369
[TBL] [Abstract][Full Text] [Related]
14. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
Kärppä M; Herva R; Moslemi AR; Oldfors A; Kakko S; Majamaa K
Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
[TBL] [Abstract][Full Text] [Related]
15. Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation.
Yorifuji T; Kawai M; Momoi T; Sasaki H; Furusho K; Muroi J; Shimizu K; Takahashi Y; Matsumura M; Nambu M; Okuno T
J Med Genet; 1996 Jul; 33(7):621-2. PubMed ID: 8818955
[TBL] [Abstract][Full Text] [Related]
16. Progressive depletion of mtDNA in mitochondrial myopathy.
Durham SE; Brown DT; Turnbull DM; Chinnery PF
Neurology; 2006 Aug; 67(3):502-4. PubMed ID: 16894115
[TBL] [Abstract][Full Text] [Related]
17. A case of membranous nephropathy associated with chronic sinusitis.
Kanazawa I; Yano S; Takase H; Yamane Y; Yamaguchi T; Sugimoto T
J Nephrol; 2009; 22(2):289-94. PubMed ID: 19384848
[TBL] [Abstract][Full Text] [Related]
18. A case of living-related renal transplant from the donor with membranous nephropathy.
Akioka K; Okamoto M; Ushigome H; Nobori S; Suzuki T; Sakai K; Sakamoto S; Urasaki K; Yanagisawa A; Fukatsu A; Yoshimura N
Clin Transplant; 2009 Aug; 23 Suppl 20():62-6. PubMed ID: 19594600
[TBL] [Abstract][Full Text] [Related]
19. [The incidence of renal diseases as diagnosed by biopsy in Hungary].
Sipiczki T; Ondrik Z; Abrahám G; Pokorny G; Túri S; Sonkodi S; Kemény E; Iványi B
Orv Hetil; 2004 Jun; 145(26):1373-9. PubMed ID: 15384747
[TBL] [Abstract][Full Text] [Related]
20. Horseshoe kidney with PLA2R-positive membranous nephropathy.
Shi SS; Yang XZ; Zhang XY; Guo HD; Wang WF; Zhang L; Wu P; Zhang W; Wen WB; Huo XL; Zhang YQ
BMC Nephrol; 2021 Aug; 22(1):277. PubMed ID: 34376183
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
