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Items: 1 to 20 of 84

1.
Acquired Bartter-like syndrome associated with colistin use in an adult patient: a case report
Ameneh Sari, Mohammadreza Fadavipour, Samaneh Hashemi
CEN Case Rep. 2024 Dec; 13(6): 557–560. Published online 2024 May 21. doi: 10.1007/s13730-024-00891-1
PMCID:
PMC11608191
AbstractArticlePDF–416K
2.
Bartter Syndrome Presenting as Arginine-Vasopressin Resistance: A Report of 2 Cases
Maria Sousa, Regina Medeiros, Ana Luísa Rodrigues, Bernardo Dias Pereira
Am J Case Rep. 2024; 25: e942872-1–e942872-9. Published online 2024 Jun 17. doi: 10.12659/AJCR.942872
PMCID:
PMC11196210
AbstractArticlePDF–2.7M
3.
First Diagnosis of Gitelman Syndrome During Pregnancy in an Adolescent Female: A Case Report
Konstantinos Zacharis, Chalent Alexakis, Vasiliki K Tsapadikou, Ismini Anagnostaki, Theodoros Charitos
Cureus. 2024 May; 16(5): e59644. Published online 2024 May 4. doi: 10.7759/cureus.59644
PMCID:
PMC11146675
AbstractArticlePDF–394K
4.
Pseudo-Gitelman Syndrome Presenting with Hypokalemic Metabolic Alkalosis and Hypocalciuria
Seung Heon Lee, Sukyung Lee, Hyunsung Kim, Gheun-Ho Kim
Electrolyte Blood Press. 2023 Dec; 21(2): 72–76. Published online 2023 Dec 18. doi: 10.5049/EBP.2023.21.2.72
PMCID:
PMC10751206
AbstractArticlePDF–1.3M
5.
Bartter Syndrome: A Systematic Review of Case Reports and Case Series
Rakhtan K. Qasba, Anna Carolina Flumignan Bucharles, Maria Victoria Ferreira Piccoli, Pranjal Sharma, Akshat Banga, Balakrishnan Kamaraj, Faisal A. Nawaz, Harshadayani Jagadish Kumar, Mahika Afrin Happy, Ruman K. Qasba, Gowthami Sai Kogilathota Jagirdhar, Mohammad Yasir Essar, Piyush Garg, Shiva Teja Reddy, Kaanthi Rama, Salim Surani, Rahul Kashyap
Medicina (Kaunas) 2023 Sep; 59(9): 1638. Published online 2023 Sep 11. doi: 10.3390/medicina59091638
PMCID:
PMC10537044
AbstractArticlePDF–1.7M
6.
A Novel Mutation in Cystic Fibrosis Presenting as Pseudo Bartter Syndrome: A Case Report
Seema Shah, Sunil Jondhale, Manas Ranjan Sahoo, Tushar Jagzape, Swasti Keshri, Anil Kumar Goel
Indian J Clin Biochem. 2023 Oct; 38(4): 550–552. Published online 2021 Oct 7. doi: 10.1007/s12291-021-01010-y
PMCID:
PMC10516826
AbstractArticlePDF–149K
7.
Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3
Alejandro García-Castaño, Sara Gómez-Conde, Leire Gondra, María Herrero, Mireia Aguirre, Ana-Belén de la Hoz, Luis Castaño, Renaltube group, Leire Madariaga
Sci Rep. 2023; 13: 12587. Published online 2023 Aug 3. doi: 10.1038/s41598-023-38179-6
PMCID:
PMC10400606
AbstractArticlePDF–997K
8.
Cardiovascular Remodeling in Chronic Mineralocorticoid Excess
Pradnya Brijmohan Bhattad, Mazen Roumia
Cureus. 2023 Jun; 15(6): e40753. Published online 2023 Jun 21. doi: 10.7759/cureus.40753
PMCID:
PMC10361634
AbstractArticlePDF–551K
9.
Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing
Luyang Yang, Jinmeng Fan, Yunfeng Liu, Yi Ren, Zekun Liu, Hairui Fu, Hao Qi, Jing Yang
Medicine (Baltimore) 2023 Jun 16; 102(24): e33959. Published online 2023 Jun 16. doi: 10.1097/MD.0000000000033959
PMCID:
PMC10270490
AbstractArticlePDF–650K
10.
Gitelman Syndrome: A Case Report
João Rocha, Mariana Pacheco, Mariana Matos, Susana Ferreira, Jorge S Almeida
Cureus. 2023 May; 15(5): e38418. Published online 2023 May 2. doi: 10.7759/cureus.38418
PMCID:
PMC10234615
AbstractArticlePDF–107K
11.
Late-Onset Bartter’s Syndrome Type II with End-Stage Renal Disease Due to a Novel Mutation in KCNJ1 Gene in an Indian Adult Male – A Case Report
Payal Gaggar, D Sree Bhushan Raju, M Ravi Tej, P Pragna
Indian J Nephrol. 2023 Jan-Feb; 33(1): 57–60. Published online 2022 Sep 29. doi: 10.4103/ijn.ijn_383_21
PMCID:
PMC10185019
AbstractArticlePDF–1.2M
12.
Novel Intronic Mutations of the SLC12A3 Gene in Patients with Gitelman Syndrome
Zeli Xun, Pengfei Gao, Yanan Du, Xue Yan, Jingmin Yang, Zhihua Wang
Int J Gen Med. 2023; 16: 1797–1806. Published online 2023 May 11. doi: 10.2147/IJGM.S408631
PMCID:
PMC10184854
AbstractArticlePDF–3.8M
13.
Diagnostic Accuracy of Acid-Base Status in Infants with Hypertrophic Pyloric Stenosis
Marko Bašković, Dorotea Sinjeri
Children (Basel) 2022 Dec; 9(12): 1815. Published online 2022 Nov 24. doi: 10.3390/children9121815
PMCID:
PMC9776884
AbstractArticlePDF–1019K
14.
Postoperative apnea after pyloromyotomy for infantile hypertrophic pyloric stenosis
Anna Camporesi, Veronica Diotto, Elena Zoia, Simone Rotta, Federica Tarantino, Laura Maria Giuditta Eccher, Valeria Calcaterra, Gloria Pelizzo, Marco Gemma
World J Pediatr Surg. 2022; 5(3): e000391. Published online 2022 May 19. doi: 10.1136/wjps-2021-000391
PMCID:
PMC9716955
AbstractArticlePDF–558K
15.
Diagnosis of Adrenocortical Carcinoma with Hypercortisolism in a Patient Presenting with Hypokalemic Metabolic Alkalosis
Omair Khan, Sheharyar Raashid, Muhammad Hashim, Kevin Clements, Sanjay Maheshwari, Syed M. Mazhar Uddin, Pranay Siriya, Aftab Vadsariya, Patricia Park, William Pascal
J Community Hosp Intern Med Perspect. 2022; 12(5): 114–118. Published online 2022 Sep 9. doi: 10.55729/2000-9666.1108
PMCID:
PMC9529648
AbstractArticlePDF–1.1M
16.
Anesthetic management of child with Gitelman Syndrome: case report
Sara Ferreira, Cláudia Antunes, Marta Pereira, Susana Rodrigues
Braz J Anesthesiol. 2021 Sep-Oct; 71(5): 588–590. Published online 2021 Jun 6. doi: 10.1016/j.bjane.2021.05.003
PMCID:
PMC9373332
AbstractArticlePDF–292K
17.
Gitelman syndrome with normocalciuria – a case report
Mariusz Flisiński, Ewa Skalska, Barbara Mączyńska, Natalia Butt-Hussaim, Agnieszka Sobczyńska-Tomaszewska, Olga Haus, Jacek Manitius
BMC Nephrol. 2022; 23: 170. Published online 2022 May 4. doi: 10.1186/s12882-022-02782-y
PMCID:
PMC9069753
AbstractArticlePDF–1.2M
18.
Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review
Mi Tian, Hui Peng, Xin Bi, Yan-Qiu Wang, Yong-Zhe Zhang, Yan Wu, Bei-Ru Zhang
Front Med (Lausanne) 2022; 9: 862514. Published online 2022 Apr 7. doi: 10.3389/fmed.2022.862514
PMCID:
PMC9021870
AbstractArticlePDF–1.2M
19.
EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies
Jacky Lo, Anna-Lena Forst, Richard Warth, Anselm A. Zdebik
Front Physiol. 2022; 13: 852674. Published online 2022 Mar 15. doi: 10.3389/fphys.2022.852674
PMCID:
PMC8965613
AbstractArticlePDF–4.4M
20.
Renal calcium and magnesium handling in Gitelman syndrome
Jeremiah V Reyes, Paul Mark B Medina
Am J Transl Res. 2022; 14(1): 1–19. Published online 2022 Jan 15.
PMCID:
PMC8829599
AbstractArticlePDF–1.2M

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