Variants in genes coding for collagen type IV α-chains are frequent causes of persistent, isolated hematuria during childhood-Reference-Cited by-同舟云学术

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Variants in genes coding for collagen type IV α-chains are frequent causes of persistent, isolated hematuria during childhood

Published:2022-06-27 Issue:3 Volume:38 Page:687-695
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Alge Joseph L.,Bekheirnia Nasim,Willcockson Alexandra R.,Qin Xiang,Scherer Steven E.,Braun Michael C.,Bekheirnia Mir Reza

Funder

Baylor College of Medicine

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00467-022-05627-w.pdf

Reference43 articles.

1. Vehaskari VM, Rapola J, Koskimies O, Savilahti E, Vilska J, Hallman N (1979) Microscopic hematuria in school children: epidemiology and clinicopathologic evaluation. J Pediatr 95:676–684

2. Vivante A, Afek A, Frenkel-Nir Y, Tzur D, Farfel A, Golan E, Chaiter Y, Shohat T, Skorecki K, Calderon-Margalit R (2011) Persistent asymptomatic isolated microscopic hematuria in Israeli adolescents and young adults and risk for end-stage renal disease. JAMA 306:729–736. https://doi.org/10.1001/jama.2011.1141

3. Moreno JA, Yuste C, Gutiérrez E, Sevillano ÁM, Rubio-Navarro A, Amaro-Villalobos JM, Praga M, Egido J (2016) Haematuria as a risk factor for chronic kidney disease progression in glomerular diseases: a review. Pediatr Nephrol 31:523–533. https://doi.org/10.1007/s00467-015-3119-1

4. Túri S, Visy M, Vissy A, Jászai V, Czirbesz Z, Haszon I, Szelid Z, Ferkis I (1989) Long-term follow-up of patients with persistent/recurrent, isolated haematuria: a Hungarian multicentre study. Pediatr Nephrol 3:235–239. https://doi.org/10.1007/BF00858521

5. Feng CY, Xia YH, Wang WJ, Xia J, Fu HD, Wang X, Shen HJ, Qian GL, Liu AM, Mao JH (2013) Persistent asymptomatic isolated hematuria in children: clinical and histopathological features and prognosis. World J Pediatr 9:163–168. https://doi.org/10.1007/s12519-013-0415-3

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3. CyclosporinA Derivative as Therapeutic Candidate for Alport Syndrome by Inducing Mutant Type IV Collagen Secretion;Kidney360;2023-05-05

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