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 *

215 related articles for article (PubMed ID: 35787602)

  • 1. Diagnostic Challenge of Congenital Chloride Diarrhea and Ulcerative Colitis Overlap in an Adult Misdiagnosed with Bartter Syndrome: Case Report and Literature Review.
    Sadagah LF; Makeen AZ; Kotbi ET
    Am J Case Rep; 2022 Jul; 23():e936715. PubMed ID: 35787602
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital chloride diarrhea misdiagnosed as Bartter syndrome.
    Eğrıtaş O; Dalgiç B; Wedenoja S
    Turk J Gastroenterol; 2011 Jun; 22(3):321-3. PubMed ID: 21805424
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pseudo-Bartter syndrome in an infant with congenital chloride diarrhoea.
    Igrutinović Z; Peco-Antić A; Radlović N; Vuletić B; Marković S; Vujić A; Rasković Z
    Srp Arh Celok Lek; 2011; 139(9-10):677-80. PubMed ID: 22070007
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Congenital chloride diarrhea misdiagnosed as pseudo-Bartter syndrome.
    Saneian H; Bahraminia E
    J Res Med Sci; 2013 Sep; 18(9):822-4. PubMed ID: 24381629
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The utility of next generation sequencing in the correct diagnosis of congenital hypochloremic hypokalemic metabolic alkalosis.
    Ben-David Y; Halevy R; Sakran W; Zehavi Y; Spiegel R
    Eur J Med Genet; 2019 Oct; 62(10):103728. PubMed ID: 31325522
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cystic Fibrosis Presenting as Pseudo-Bartter Syndrome: An Important Diagnosis that is Missed!
    Mantoo MR; Kabra M; Kabra SK
    Indian J Pediatr; 2020 Sep; 87(9):726-732. PubMed ID: 32504456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Classic Bartter syndrome: a rare cause of failure to thrive in a child.
    Vieira H; Mendes L; Mendes P; da Silva JE
    BMJ Case Rep; 2012 Jun; 2012():. PubMed ID: 22744244
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypochloremic metabolic alkalosis and failure to thrive: answer.
    Querfeld U; Lechner S; Janecke AR
    Pediatr Nephrol; 2011 Jun; 26(6):895-6. PubMed ID: 20981452
    [No Abstract]   [Full Text] [Related]  

  • 11. Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: a case report.
    Dávid É; Török D; Farkas K; Nagy N; Horváth E; Kiss Z; Oroszlán G; Balogh M; Széll M
    BMC Pediatr; 2019 Jan; 19(1):16. PubMed ID: 30635044
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes.
    Shaer AJ
    Am J Med Sci; 2001 Dec; 322(6):316-32. PubMed ID: 11780689
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Antenatal Bartter Syndrome: A Case Report.
    Akther M; Moni SC; Jahan I; Shabuj KH; Dey SK; Mannan MA; Shahidullah M
    Mymensingh Med J; 2020 Apr; 29(2):469-472. PubMed ID: 32506108
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Two Cases of Pseudo-Bartter Syndrome in Childhood: When to Suspect a Rare Onset Pattern of Cystic Fibrosis].
    Vergine G; Fressola G; Ambroni M; Gessaroli M; Bigucci B; Mazzocco M; Conte ML
    G Ital Nefrol; 2024 Jun; 41(3):. PubMed ID: 38943326
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Turkish case of congenital chloride diarrhea with SLC26A3 gene (c.2025_2026insATC) mutation: diagnostic pitfalls.
    Özbay Hoşnut F; Karadağ Öncel E; Öncel MY; Özcay F
    Turk J Gastroenterol; 2010 Dec; 21(4):443-7. PubMed ID: 21332001
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis.
    Sun M; Tao N; Liu X; Yang Y; Su Y; Xu F
    Pediatr Endocrinol Diabetes Metab; 2021; 27(1):51-56. PubMed ID: 33599438
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Acquired autoimmune Bartter syndrome in a patient with primary hypothyroidism.
    Nasir N; Mohanty D; Pande AK; Khanna D; Vishvakarma K; Gupta L
    Rheumatol Int; 2023 Mar; 43(3):567-574. PubMed ID: 34800134
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5.
    Okamoto T; Tajima T; Hirayama T; Sasaki S
    Eur J Pediatr; 2012 Feb; 171(2):401-4. PubMed ID: 21932010
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bartter-like Syndrome Induced By Tacrolimus in a Renal Transplanted Boy: A Case Report.
    Dias RF; da Costa Monteiro M; Silva RAM; Diniz MML; Simões E Silva AC
    Curr Drug Saf; 2023; 18(3):398-403. PubMed ID: 35593330
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.