Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy-Reference-Cited by-同舟云学术

Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

Published:2022-09 Issue:3 Volume:102 Page:592-603
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Drovandi Stefania^ORCID,Lipska-Ziętkiewicz Beata S.^ORCID,Ozaltin Fatih,Emma Francesco,Gulhan Bora,Boyer Olivia,Trautmann Agnes,Ziętkiewicz Szymon,Xu Hong,Shen Qian,Rao Jia,Riedhammer Korbinian M.^ORCID,Heemann Uwe,Hoefele Julia^ORCID,Stenton Sarah L.,Tsygin Alexey N.,Ng Kar-Hui,Fomina Svitlana,Benetti Elisa,Aurelle Manon,Prikhodina Larisa,Schijvens Anne M.,Tabatabaeifar Mansoureh,Jankowski Maciej,Baiko Sergey,Mao Jianhua,Feng Chunyue,Deng Fang,Rousset-Rouviere Caroline,Stańczyk Małgorzata,Bałasz-Chmielewska Irena,Fila Marc,Durkan Anne M.,Levart Tanja Kersnik,Dursun Ismail,Esfandiar Nasrin,Haas Dorothea,Bjerre Anna,Anarat Ali,Benz Marcus R.,Talebi Saeed,Hooman Nakysa,Ariceta Gema,Schaefer Franz,Baiko Sergey,Serna Higuita Lina Maria,Schaefer Franz,Trautmann Agnes,Tabatabaeifar Mansoureh,Gheissari Alaleh,Hooman Nakysa,Benetti Elisa,Emma Francesco,Nigmatullina Nazym,Lipska-Ziętkiewicz Beata S.,Bałasz-Chmielewska Irena,Tkaczyk Marcin,Stańczyk Małgorzata,Borzecka Halina,Tsygin Alexey N.,Prikhodina Larisa,Bogdanovic Radovan,Anarat Ali,Ozaltin Fatih,Mir Sevgi,Fomina Svitlana,Klopstock Thomas,Prokisch Holger,Kornblum Cornelia,Xu Hong,Shen Qian,Rao Jia,Liu Cui-Hua,Sun Shu-Zhen,Deng Fang,Dong Yang,Wang Xiao-Wen,Luan Jiang-Wei

Publisher

Elsevier BV

Subject

Nephrology

Reference21 articles.

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3. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort;Trautmann;Clin J Am Soc Nephrol,2015

4. A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome;Sadowski;J Am Soc Nephrol,2015

5. Mitochondrial disease and the kidney with a special focus on CoQ10 deficiency;Schijvens;Kidney Int Rep,2020

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1. Familial thrombotic microangiopathy in a child with coenzyme Q10 deficiency-associated glomerulopathy;Pediatric Nephrology;2024-09-03

2. Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa;The American Journal of Human Genetics;2024-09

3. Coenzyme Q10 and embryonic development: a potential role in reproductive medicine;Obstetrics, Gynecology and Reproduction;2024-08-13

4. Identification of CUBN variants in triplets with a 20-year history of proteinuria;CEN Case Reports;2024-08-05

5. Glomerular basement membrane ultrastructural changes in a patient with COQ2 glomerulopathy: A case report;Nephrology;2024-06-04