These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 12836094)

  • 1. Bartter syndrome complicated by immune complex nephropathy. Case report and literature review.
    Sardani Y; Qin K; Haas M; Aronson AJ; Rosenfield RL
    Pediatr Nephrol; 2003 Sep; 18(9):913-8. PubMed ID: 12836094
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome.
    Bettinelli A; Borsa N; Syrén ML; Mattiello C; Coviello D; Edefonti A; Giani M; Travi M; Tedeschi S
    Pediatr Res; 2005 Dec; 58(6):1269-73. PubMed ID: 16306206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel CLCNKB mutation in a Chinese girl with classic Bartter syndrome: a case report.
    Zhu B; Jiang H; Cao M; Zhao X; Jiang H
    BMC Med Genet; 2019 Aug; 20(1):137. PubMed ID: 31409296
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.
    Jeck N; Konrad M; Peters M; Weber S; Bonzel KE; Seyberth HW
    Pediatr Res; 2000 Dec; 48(6):754-8. PubMed ID: 11102542
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
    Andrini O; Keck M; Briones R; Lourdel S; Vargas-Poussou R; Teulon J
    Am J Physiol Renal Physiol; 2015 Jun; 308(12):F1324-34. PubMed ID: 25810436
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Renal cysts and nephrocalcinosis in a patient with Bartter syndrome type III.
    Watanabe T; Tajima T
    Pediatr Nephrol; 2005 May; 20(5):676-8. PubMed ID: 15717167
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.
    Rodríguez-Soriano J; Vallo A; Pérez de Nanclares G; Bilbao JR; Castaño L
    Pediatr Nephrol; 2005 Jul; 20(7):891-6. PubMed ID: 15875219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Predominant but silent C1q deposits in mesangium on transplanted kidneys - long-term observational study.
    Kanai T; Akioka Y; Miura K; Hisano M; Koike J; Yamaguchi Y; Hattori M
    BMC Nephrol; 2018 Apr; 19(1):82. PubMed ID: 29625558
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.
    Zelikovic I; Szargel R; Hawash A; Labay V; Hatib I; Cohen N; Nakhoul F
    Kidney Int; 2003 Jan; 63(1):24-32. PubMed ID: 12472765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome.
    Tajima T; Nawate M; Takahashi Y; Mizoguchi Y; Sugihara S; Yoshimoto M; Murakami M; Adachi M; Tachibana K; Mochizuki H; Fujieda K
    Endocr J; 2006 Oct; 53(5):647-52. PubMed ID: 16902263
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome.
    Chiang WF; Lin SH; Chan JS; Lin SH
    Clin Nephrol; 2014 Feb; 81(2):146-50. PubMed ID: 22854165
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adult presentation of Bartter syndrome type IV with erythrocytosis.
    Heilberg IP; Tótoli C; Calado JT
    Einstein (Sao Paulo); 2015; 13(4):604-6. PubMed ID: 26537508
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Progress of research on the role of CLCNKB gene in classical Bartter syndrome].
    Zhou J; Wang C; Bao H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):573-577. PubMed ID: 32335890
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations.
    Giri D; Bockenhauer D; Deshpande C; Achermann JC; Taylor NF; Rumsby G; Morgan H; Senniappan S; Ajzensztejn M
    Horm Res Paediatr; 2020; 93(2):137-142. PubMed ID: 32506065
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Bartter syndrome type 3: an unusual cause of nephrolithiasis.
    Colussi G; De Ferrari ME; Tedeschi S; Prandoni S; Syrén ML; Civati G
    Nephrol Dial Transplant; 2002 Mar; 17(3):521-3. PubMed ID: 11865110
    [No Abstract]   [Full Text] [Related]  

  • 16. Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.
    Nozu K; Inagaki T; Fu XJ; Nozu Y; Kaito H; Kanda K; Sekine T; Igarashi T; Nakanishi K; Yoshikawa N; Iijima K; Matsuo M
    J Med Genet; 2008 Mar; 45(3):182-6. PubMed ID: 18310267
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria.
    Fukuyama S; Hiramatsu M; Akagi M; Higa M; Ohta T
    J Clin Endocrinol Metab; 2004 Nov; 89(11):5847-50. PubMed ID: 15531551
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bartter syndrome and growth hormone deficiency: Three siblings with a novel CLCNKB mutation.
    Brambilla I; Poddighe D; Semeria Mantelli S; Guarracino C; Marseglia GL
    Pediatr Int; 2019 Feb; 61(2):193-197. PubMed ID: 30387909
    [No Abstract]   [Full Text] [Related]  

  • 19. Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis.
    Najafi M; Kordi-Tamandani DM; Behjati F; Sadeghi-Bojd S; Bakey Z; Karimiani EG; Schüle I; Azarfar A; Schmidts M
    Orphanet J Rare Dis; 2019 Feb; 14(1):41. PubMed ID: 30760291
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Renal dysfunction and barttin expression in Bartter syndrome Type IV associated with a G47R mutation in BSND in a family.
    Park CW; Lim JH; Youn DY; Chung S; Lim MH; Kim YK; Chang YS; Lee JH
    Clin Nephrol; 2011 Feb; 75 Suppl 1():69-74. PubMed ID: 21269598
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.