150 related articles for article (PubMed ID: 36843884)
1. Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases.
Liang R; Chen X; Zhang Y; Law CF; Yu S; Jiao J; Yang Q; Wu D; Zhang G; Chen H; Wang M; Yang H; Wang A
Front Pediatr; 2022; 10():1030191. PubMed ID: 36843884
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. COQ8B glomerular nephropathy: Outcomes after kidney transplantation and analysis of characteristics in Chinese population.
Zeng S; Xu Y; Cheng C; Yu N; Liu L; Mo Y; Chen L; Jiang X
Front Pediatr; 2022; 10():938863. PubMed ID: 36034551
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A case report of adult-onset COQ8B nephropathy presenting focal segmental glomerulosclerosis with granular swollen podocytes.
Maeoka Y; Doi T; Aizawa M; Miyasako K; Hirashio S; Masuda Y; Kishita Y; Okazaki Y; Murayama K; Imasawa T; Hara S; Masaki T
BMC Nephrol; 2020 Aug; 21(1):376. PubMed ID: 32859164
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Drovandi S; Lipska-Ziętkiewicz BS; Ozaltin F; Emma F; Gulhan B; Boyer O; Trautmann A; Xu H; Shen Q; Rao J; Riedhammer KM; Heemann U; Hoefele J; Stenton SL; Tsygin AN; Ng KH; Fomina S; Benetti E; Aurelle M; Prikhodina L; Schreuder MF; Tabatabaeifar M; Jankowski M; Baiko S; Mao J; Feng C; Liu C; Sun S; Deng F; Wang X; Clavé S; Stańczyk M; Bałasz-Chmielewska I; Fila M; Durkan AM; Levart TK; Dursun I; Esfandiar N; Haas D; Bjerre A; Anarat A; Benz MR; Talebi S; Hooman N; Ariceta G; ; ; ; Schaefer F
Kidney Int; 2022 Sep; 102(3):604-612. PubMed ID: 35643375
[TBL] [Abstract][Full Text] [Related]
8. Primary coenzyme Q10 Deficiency-6 (COQ10D6): Two siblings with variable expressivity of the renal phenotype.
Yuruk Yildirim Z; Toksoy G; Uyguner O; Nayir A; Yavuz S; Altunoglu U; Turkkan ON; Sevinc B; Gokcay G; Kurkcu Gunes D; Kiyak A; Yilmaz A
Eur J Med Genet; 2020 Jan; 63(1):103621. PubMed ID: 30682496
[TBL] [Abstract][Full Text] [Related]
9. The role of novel COQ8B mutations in glomerulopathy and related kidney defects.
AbuMaziad AS; Thaker TM; Tomasiak TM; Chong CC; Galindo MK; Hoyme HE
Am J Med Genet A; 2021 Jan; 185(1):60-67. PubMed ID: 33084234
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. COQ8B-Related Steroid-Resistant Nephrotic Syndrome in Saudi Arabia: A Case Report.
Alvi NH; Turkstani BA; Ashi AS; Alzahrani AM; Tawffeq AM
Cureus; 2022 Nov; 14(11):e31922. PubMed ID: 36532926
[TBL] [Abstract][Full Text] [Related]
12. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis.
Park E; Lee C; Kim NKD; Ahn YH; Park YS; Lee JH; Kim SH; Cho MH; Cho H; Yoo KH; Shin JI; Kang HG; Ha IS; Park WY; Cheong HI
J Clin Med; 2020 Jun; 9(6):. PubMed ID: 32604935
[TBL] [Abstract][Full Text] [Related]
13. Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Drovandi S; Lipska-Ziętkiewicz BS; Ozaltin F; Emma F; Gulhan B; Boyer O; Trautmann A; Ziętkiewicz S; Xu H; Shen Q; Rao J; Riedhammer KM; Heemann U; Hoefele J; Stenton SL; Tsygin AN; Ng KH; Fomina S; Benetti E; Aurelle M; Prikhodina L; Schijvens AM; Tabatabaeifar M; Jankowski M; Baiko S; Mao J; Feng C; Deng F; Rousset-Rouviere C; Stańczyk M; Bałasz-Chmielewska I; Fila M; Durkan AM; Levart TK; Dursun I; Esfandiar N; Haas D; Bjerre A; Anarat A; Benz MR; Talebi S; Hooman N; Ariceta G; ; ; ; Schaefer F
Kidney Int; 2022 Sep; 102(3):592-603. PubMed ID: 35483523
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. C1q nephropathy: a variant of focal segmental glomerulosclerosis.
Markowitz GS; Schwimmer JA; Stokes MB; Nasr S; Seigle RL; Valeri AM; D'Agati VD
Kidney Int; 2003 Oct; 64(4):1232-40. PubMed ID: 12969141
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Clinical and pathological features and mutational types of WT1 mutation-associated nephropathy].
Sun LZ; Wang HY; Li M; Lin HR; Wu JL; Tang W; Li YJ; Yue ZH; Liu T; Chen HM; Hu MY
Zhonghua Er Ke Za Zhi; 2018 Oct; 56(10):769-774. PubMed ID: 30293282
[No Abstract] [Full Text] [Related]
18. Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases.
Liang R; Chen X; Zhang Y; Law CF; Yu S; Jiao J; Yang Q; Wu D; Zhang G; Chen H; Wang M; Yang H; Wang A
Front Pediatr; 2023; 11():1183013. PubMed ID: 37063683
[TBL] [Abstract][Full Text] [Related]
19.
Li M; Yue Z; Lin H; Wang H; Chen H; Sun L
Ren Fail; 2021 Dec; 43(1):97-101. PubMed ID: 33397173
[TBL] [Abstract][Full Text] [Related]
20. [Four cases of nephrotic syndrome with TRPC6 gene variations and literature review].
Sun LW; Sun L; Wang P; Kang YL; Wu Y; Zhu GH; Huang WY
Zhonghua Er Ke Za Zhi; 2021 Mar; 59(3):223-227. PubMed ID: 33657698
[No Abstract] [Full Text] [Related]
[Next] [New Search]
