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OpenAlex Citation Counts

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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:

Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance
Laura Florea, Lavinia Caba, Eusebiu Vlad Gorduza
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 13

Showing 13 citing articles:

APOL1 and APOL1-Associated Kidney Disease: A Common Disease, an Unusual Disease Gene – Proceedings of the Henry Shavelle Professorship
Martin R. Pollak, David J. Friedman
Glomerular Diseases (2023), pp. 75-87
Open Access | Times Cited: 12
Pathophysiologic approach in genetic hypokalemia: An update
Anne Blanchard
Annales d Endocrinologie (2023) Vol. 84, Iss. 2, pp. 298-307
Open Access | Times Cited: 4
Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in Korea
Naye Choi, Seong Heon Kim, Eun Hui Bae, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 4
Chemotherapy-induced tubulopathy: a case report series
Mario Alamilla-Sanchez, Juan Daniel Díaz García, Valeria Yanez Salguero, et al.
Frontiers in Nephrology (2024) Vol. 4
Open Access
Study of the Pathogenesis of CF-PBS and BS
佰丽 翁
Advances in Clinical Medicine (2024) Vol. 14, Iss. 08, pp. 331-338
Closed Access
Epidemiological point of view
Seyedeh Fatemeh Hosseini, Ci Weimin, Parsa Nikoofar
Elsevier eBooks (2024), pp. 3-24
Closed Access
SLC12A1 variant c.1684+1 G>A causes Bartter syndrome type 1 by promoting exon 13 skipping
Wenke Yang, Yanjun Li, Zhenglong Guo, et al.
Nephrology (2024)
Closed Access
40 Years experience in Bartter’s syndrome
Laura García Espinosa, Alejandro Zarauza Santoveña, Juan Bravo Feito, et al.
Nefrología (English Edition) (2024) Vol. 44, Iss. 5, pp. 766-768
Open Access
From Fish Physiology to Human Disease: The Discovery of the NCC, NKCC2, and the Cation-Coupled Chloride Cotransporters
Gerardo Gamba
Kidney360 (2023) Vol. 5, Iss. 1, pp. 133-141
Open Access | Times Cited: 1
Metabolic alkalosis in cystic fibrosis: from vascular volume depletion to impaired bicarbonate excretion
Manoocher Soleimani
Frontiers in Endocrinology (2024) Vol. 15
Open Access
Bartter Syndrome Type 1 Due to Novel SLC12A1 Mutations Associated With Pseudohypoparathyroidism Type II
Zentaro Kiuchi, Kandai Nozu, Kunimasa Yan, et al.
JCEM Case Reports (2023) Vol. 1, Iss. 2
Open Access
40 años de experiencia en síndrome de Bartter
Laura García Espinosa, Alejandro Zarauza Santoveña, Juan Bravo Feito, et al.
Nefrología (2023) Vol. 44, Iss. 5, pp. 766-768
Open Access
Bartter Syndrome: Perspectives of a Pediatric Nephrologist
Naye Choi, Hee Gyung Kang
Electrolytes & Blood Pressure (2022) Vol. 20, Iss. 2, pp. 49-49
Open Access
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