
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
A Current Landscape on Alport Syndrome Cases: Characterization, Therapy and Management Perspectives
Nahed N. Mahrous, Yahya F. Jamous, Ahmed Almatrafi, et al.
Biomedicines (2023) Vol. 11, Iss. 10, pp. 2762-2762
Open Access | Times Cited: 4
Nahed N. Mahrous, Yahya F. Jamous, Ahmed Almatrafi, et al.
Biomedicines (2023) Vol. 11, Iss. 10, pp. 2762-2762
Open Access | Times Cited: 4
Showing 4 citing articles:
The known and unknown about attention deficit hyperactivity disorder (ADHD) genetics: a special emphasis on Arab population
Nahed N. Mahrous, Amirah Albaqami, Rimah Saleem, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Nahed N. Mahrous, Amirah Albaqami, Rimah Saleem, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 2
Exploration of Gene Therapy for Alport Syndrome
Yafei Zhao, Qimin Zheng, Jingyuan Xie
Biomedicines (2024) Vol. 12, Iss. 6, pp. 1159-1159
Open Access
Yafei Zhao, Qimin Zheng, Jingyuan Xie
Biomedicines (2024) Vol. 12, Iss. 6, pp. 1159-1159
Open Access
A importância do diagnóstico precoce e das intervenções terapêuticas na Síndrome de Alport
Gianynne Felicidade Silva Santos, Kaio Oliveira Costa, Lucas Lopes, et al.
Brazilian Journal of Health Review (2024) Vol. 7, Iss. 4, pp. e71674-e71674
Open Access
Gianynne Felicidade Silva Santos, Kaio Oliveira Costa, Lucas Lopes, et al.
Brazilian Journal of Health Review (2024) Vol. 7, Iss. 4, pp. e71674-e71674
Open Access
Synergistic toxicity of compound heterozygous mutations in the COL4A3 gene causes end-stage renal disease in A large family of Alport syndrome
Longxin Xie, Yuxi Ding, Ying Qiu, et al.
Gene (2024), pp. 149132-149132
Closed Access
Longxin Xie, Yuxi Ding, Ying Qiu, et al.
Gene (2024), pp. 149132-149132
Closed Access