162 related articles for article (PubMed ID: 28298181)
1. Early-onset of ADCK4 glomerulopathy with renal failure: a case report.
Lolin K; Chiodini BD; Hennaut E; Adams B; Dahan K; Ismaili K
BMC Med Genet; 2017 Mar; 18(1):28. PubMed ID: 28298181
[TBL] [Abstract][Full Text] [Related]
2. Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations.
Park E; Kang HG; Choi YH; Lee KB; Moon KC; Jeong HJ; Nagata M; Cheong HI
Pediatr Nephrol; 2017 Sep; 32(9):1547-1554. PubMed ID: 28405841
[TBL] [Abstract][Full Text] [Related]
3. Early-onset COQ8B (ADCK4) glomerulopathy in a child with isolated proteinuria: a case report and literature review.
Zhai SB; Zhang L; Sun BC; Zhang Y; Ma QS
BMC Nephrol; 2020 Sep; 21(1):406. PubMed ID: 32957916
[TBL] [Abstract][Full Text] [Related]
4. Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment.
Atmaca M; Gulhan B; Korkmaz E; Inozu M; Soylemezoglu O; Candan C; Bayazıt AK; Elmacı AM; Parmaksiz G; Duzova A; Besbas N; Topaloglu R; Ozaltin F
Pediatr Nephrol; 2017 Aug; 32(8):1369-1375. PubMed ID: 28337616
[TBL] [Abstract][Full Text] [Related]
5. ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS.
Korkmaz E; Lipska-Ziętkiewicz BS; Boyer O; Gribouval O; Fourrage C; Tabatabaei M; Schnaidt S; Gucer S; Kaymaz F; Arici M; Dinckan A; Mir S; Bayazit AK; Emre S; Balat A; Rees L; Shroff R; Bergmann C; Mourani C; Antignac C; Ozaltin F; Schaefer F;
J Am Soc Nephrol; 2016 Jan; 27(1):63-8. PubMed ID: 25967120
[TBL] [Abstract][Full Text] [Related]
6. A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy.
Yang J; Yang Y; Hu Z
Biochem Biophys Res Commun; 2018 Nov; 506(3):444-449. PubMed ID: 30352687
[TBL] [Abstract][Full Text] [Related]
7. Long-term follow-up results of patients with ADCK4 mutations who have been diagnosed in the asymptomatic period: effects of early initiation of CoQ10 supplementation.
Atmaca M; Gülhan B; Atayar E; Bayazıt AK; Candan C; Arıcı M; Topaloğlu R; Özaltın F
Turk J Pediatr; 2019; 61(5):657-663. PubMed ID: 32104996
[TBL] [Abstract][Full Text] [Related]
8. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.
Ashraf S; Gee HY; Woerner S; Xie LX; Vega-Warner V; Lovric S; Fang H; Song X; Cattran DC; Avila-Casado C; Paterson AD; Nitschké P; Bole-Feysot C; Cochat P; Esteve-Rudd J; Haberberger B; Allen SJ; Zhou W; Airik R; Otto EA; Barua M; Al-Hamed MH; Kari JA; Evans J; Bierzynska A; Saleem MA; Böckenhauer D; Kleta R; El Desoky S; Hacihamdioglu DO; Gok F; Washburn J; Wiggins RC; Choi M; Lifton RP; Levy S; Han Z; Salviati L; Prokisch H; Williams DS; Pollak M; Clarke CF; Pei Y; Antignac C; Hildebrandt F
J Clin Invest; 2013 Dec; 123(12):5179-89. PubMed ID: 24270420
[TBL] [Abstract][Full Text] [Related]
9. Coenzyme Q10 supplementation therapy for 2 children with proteinuria renal disease and ADCK4 mutation: Case reports and literature review.
Feng C; Wang Q; Wang J; Liu F; Shen H; Fu H; Mao J
Medicine (Baltimore); 2017 Nov; 96(47):e8880. PubMed ID: 29382012
[TBL] [Abstract][Full Text] [Related]
10. ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment.
Widmeier E; Yu S; Nag A; Chung YW; Nakayama M; Fernández-Del-Río L; Hugo H; Schapiro D; Buerger F; Choi WI; Helmstädter M; Kim JW; Ryu JH; Lee MG; Clarke CF; Hildebrandt F; Gee HY
J Am Soc Nephrol; 2020 Jun; 31(6):1191-1211. PubMed ID: 32381600
[TBL] [Abstract][Full Text] [Related]
11. COQ8B nephropathy: Early detection and optimal treatment.
Song X; Fang X; Tang X; Cao Q; Zhai Y; Chen J; Liu J; Zhang Z; Xiang T; Qian Y; Wu B; Wang H; Zhou W; Liu C; Shen Q; Xu H; Rao J
Mol Genet Genomic Med; 2020 Aug; 8(8):e1360. PubMed ID: 32543055
[TBL] [Abstract][Full Text] [Related]
12. [Idiopathic collapsing glomerulopathy in children: report of two cases].
Wei RG; Chen SM; Jiang T; Jiang XY; Zeng Y; Mo Y
Zhonghua Er Ke Za Zhi; 2004 Oct; 42(10):731-3. PubMed ID: 16221337
[TBL] [Abstract][Full Text] [Related]
13. Association between Crohn's disease and AarF domain-containing kinase 4 glomerulopathy.
Kakiuchi T; Ohtsuka Y; Sato T; Nakayama A; Jinnouchi K; Oka M; Matsuo M
Clin J Gastroenterol; 2019 Jun; 12(3):263-268. PubMed ID: 30706428
[TBL] [Abstract][Full Text] [Related]
14. [Clinical analysis of one infantile nephrotic syndrome caused by COQ2 gene mutation and literature review].
Xu K; Mao XY; Yao Y; Cheng H; Zhang XJ
Zhonghua Er Ke Za Zhi; 2018 Sep; 56(9):662-666. PubMed ID: 30180404
[No Abstract] [Full Text] [Related]
15. ADCK4 "reenergizes" nephrotic syndrome.
Malaga-Dieguez L; Susztak K
J Clin Invest; 2013 Dec; 123(12):4996-9. PubMed ID: 24270414
[TBL] [Abstract][Full Text] [Related]
16. Idiopathic membranous nephropathy in pediatric patients: presentation, response to therapy, and long-term outcome.
Chen A; Frank R; Vento S; Crosby V; Chandra M; Gauthier B; Valderrama E; Trachtman H
BMC Nephrol; 2007 Aug; 8():11. PubMed ID: 17683621
[TBL] [Abstract][Full Text] [Related]
17. Absence of Long Noncoding RNA H19 Promotes Childhood Nephrotic Syndrome through Inhibiting ADCK4 Signal.
Xu J; Ge T; Zhou H; Zhang L; Zhao L
Med Sci Monit; 2020 Jun; 26():e922090. PubMed ID: 32489187
[TBL] [Abstract][Full Text] [Related]
18. Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.
Büscher AK; Celebi N; Hoyer PF; Klein HG; Weber S; Hoefele J
Pediatr Nephrol; 2018 Mar; 33(3):433-437. PubMed ID: 29038887
[TBL] [Abstract][Full Text] [Related]
19. CoQ10-related sustained remission of proteinuria in a child with COQ6 glomerulopathy-a case report.
Stańczyk M; Bałasz-Chmielewska I; Lipska-Ziętkiewicz B; Tkaczyk M
Pediatr Nephrol; 2018 Dec; 33(12):2383-2387. PubMed ID: 30232548
[TBL] [Abstract][Full Text] [Related]
20. Progression of minimal-change glomerulopathy to focal glomerulosclerosis in a patient with fenoprofen nephropathy.
Artinano M; Etheridge WB; Stroehlein KB; Barcenas CG
Am J Nephrol; 1986; 6(5):353-7. PubMed ID: 3826132
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]