160 related articles for article (PubMed ID: 36100451)
1. Bartter and Gitelman syndromes.
Zieg J; Doležel Z
Cas Lek Cesk; 2022; 161(3-4):131-134. PubMed ID: 36100451
[TBL] [Abstract][Full Text] [Related]
2. Molecular Basis, Diagnostic Challenges and Therapeutic Approaches of Bartter and Gitelman Syndromes: A Primer for Clinicians.
Nuñez-Gonzalez L; Carrera N; Garcia-Gonzalez MA
Int J Mol Sci; 2021 Oct; 22(21):. PubMed ID: 34768847
[TBL] [Abstract][Full Text] [Related]
3. Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathy.
Nozu K; Yamamura T; Horinouchi T; Nagano C; Sakakibara N; Ishikura K; Hamada R; Morisada N; Iijima K
Pediatr Int; 2020 Apr; 62(4):428-437. PubMed ID: 31830341
[TBL] [Abstract][Full Text] [Related]
4. Bartter Syndrome and Gitelman Syndrome.
Fulchiero R; Seo-Mayer P
Pediatr Clin North Am; 2019 Feb; 66(1):121-134. PubMed ID: 30454738
[TBL] [Abstract][Full Text] [Related]
5. [Bartter-Gitelman syndromes].
Blanchard A; Courand PY; Livrozet M; Vargas-Poussou R
Nephrol Ther; 2020 Jul; 16(4):233-243. PubMed ID: 32622651
[TBL] [Abstract][Full Text] [Related]
6. [Bartter and Gitelman syndromes].
Brochard K
Arch Pediatr; 2015 May; 22(5 Suppl 1):46-7. PubMed ID: 26112515
[No Abstract] [Full Text] [Related]
7. Understanding Bartter syndrome and Gitelman syndrome.
Fremont OT; Chan JC
World J Pediatr; 2012 Feb; 8(1):25-30. PubMed ID: 22282380
[TBL] [Abstract][Full Text] [Related]
8. Bartter's and Gitelman's syndrome.
Seyberth HW; Weber S; Kömhoff M
Curr Opin Pediatr; 2017 Apr; 29(2):179-186. PubMed ID: 27906863
[TBL] [Abstract][Full Text] [Related]
9. Bartter syndrome representing digenic-based salt-losing tubulopathies presumably accelerated by renal insufficiency.
Umene R; Kitamura M; Arai H; Matsumura K; Ishimaru Y; Maeda K; Uramatsu T; Obata Y; Mori T; Sohara E; Uchida S; Nishino T
CEN Case Rep; 2020 Nov; 9(4):375-379. PubMed ID: 32506365
[TBL] [Abstract][Full Text] [Related]
10. Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects.
Seyberth HW; Schlingmann KP
Pediatr Nephrol; 2011 Oct; 26(10):1789-802. PubMed ID: 21503667
[TBL] [Abstract][Full Text] [Related]
11. DNA analysis of renal electrolyte transporter genes among patients suffering from Bartter and Gitelman syndromes: summary of mutation screening.
Urbanová M; Reiterová J; Stěkrová J; Lněnička P; Ryšavá R
Folia Biol (Praha); 2011; 57(2):65-73. PubMed ID: 21631963
[TBL] [Abstract][Full Text] [Related]
12. Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.
Matsunoshita N; Nozu K; Yoshikane M; Kawaguchi A; Fujita N; Morisada N; Ishimori S; Yamamura T; Minamikawa S; Horinouchi T; Nakanishi K; Fujimura J; Ninchoji T; Morioka I; Nagase H; Taniguchi-Ikeda M; Kaito H; Iijima K
J Hum Genet; 2018 Jul; 63(8):887-892. PubMed ID: 29849040
[TBL] [Abstract][Full Text] [Related]
13. Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.
Corbetta S; Raimondo F; Tedeschi S; Syrèn ML; Rebora P; Savoia A; Baldi L; Bettinelli A; Pitto M
Nephrol Dial Transplant; 2015 Apr; 30(4):621-30. PubMed ID: 25422309
[TBL] [Abstract][Full Text] [Related]
14. Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome.
Palazzo V; Raglianti V; Landini S; Cirillo L; Errichiello C; Buti E; Artuso R; Tiberi L; Vergani D; Dirupo E; Romagnani P; Mazzinghi B; Becherucci F
Int J Mol Sci; 2022 May; 23(10):. PubMed ID: 35628451
[TBL] [Abstract][Full Text] [Related]
15. [Bartter syndrome and Gitelman syndrome].
Matsunoshita N; Nozu K; Iijima K
Nihon Jinzo Gakkai Shi; 2015; 57(4):743-50. PubMed ID: 26126331
[No Abstract] [Full Text] [Related]
16. Bartter and Gitelman syndromes: Questions of class.
Besouw MTP; Kleta R; Bockenhauer D
Pediatr Nephrol; 2020 Oct; 35(10):1815-1824. PubMed ID: 31664557
[TBL] [Abstract][Full Text] [Related]
17. Salt-Losing Tubulopathies in Children: What's New, What's Controversial?
Kleta R; Bockenhauer D
J Am Soc Nephrol; 2018 Mar; 29(3):727-739. PubMed ID: 29237739
[TBL] [Abstract][Full Text] [Related]
18. Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Ashton EJ; Legrand A; Benoit V; Roncelin I; Venisse A; Zennaro MC; Jeunemaitre X; Iancu D; Van't Hoff WG; Walsh SB; Godefroid N; Rotthier A; Del Favero J; Devuyst O; Schaefer F; Jenkins LA; Kleta R; Dahan K; Vargas-Poussou R; Bockenhauer D
Kidney Int; 2018 Apr; 93(4):961-967. PubMed ID: 29398133
[TBL] [Abstract][Full Text] [Related]
19. Inherited salt-losing renal tubulopathies manifesting as normotensive hypokalemic metabolic alkalosis.
Singh NP; Kaur G; Prakash A
J Assoc Physicians India; 2010 May; 58():283-4. PubMed ID: 21117345
[No Abstract] [Full Text] [Related]
20. Genetic disorders of potassium homeostasis.
Jain G; Ong S; Warnock DG
Semin Nephrol; 2013 May; 33(3):300-9. PubMed ID: 23953807
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
