Гителманов синдром (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Гителманов синдром" in Serbian language version.
refsWebsite
Global rank
Serbian rank
6th place
5th place
2,888th place
3,693rd place
archive.org (Global: 6th place; Serbian: 5th place)
- Bartter, F. C.; Pronove, P; Gill JR i sur (1962). „Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome”. The American Journal of Medicine. 33: 811—328. PMID 13969763. doi:10.1016/0002-9343(62)90214-0..
- Shaer, A. J. (2001). „Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes”. The American Journal of the Medical Sciences. 322 (6): 316—32. PMID 11780689. doi:10.1097/00000441-200112000-00004.
doi.org (Global: 2nd place; Serbian: 4th place)
- Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP (јануар 1996). „Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.”. Nat. Genet. 12 (1): 24—30. PMID 8528245. doi:10.1038/ng0196-24.
- Rodriguez-Soriano J (1998). „Bartter and related sundromes: the puzzle is almost solved”. Pediatric Nephrology. 12 (4): 315—27. PMID 9655365. doi:10.1007/s004670050461..
- Bartter, F. C.; Pronove, P; Gill JR i sur (1962). „Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome”. The American Journal of Medicine. 33: 811—328. PMID 13969763. doi:10.1016/0002-9343(62)90214-0..
- Al Shibli A, Narchi H (2015). „Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations”. World J Methodol. 5 (2): 55—61. PMC 4482822
. PMID 26140272. doi:10.5662/wjm.v5.i2.55 .. - Shaer, A. J. (2001). „Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes”. The American Journal of the Medical Sciences. 322 (6): 316—32. PMID 11780689. doi:10.1097/00000441-200112000-00004.
- Mastroianni N, De Fusco M, Zollo M, Arrigo G, Zuffardi O, Bettinelli A, Ballabio A, Casari G (август 1996). „"Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)"”. Genomics. 35 (3): 486—93. PMID 8812482. doi:10.1006/geno.1996.0388..
- Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D (2004). „Bartter's and Gitelman's syndromes: from gene to clinic”. Nephron Physiol. 96 (3): 65—78. PMID 15056980. doi:10.1159/000076752.
- Seyberth, H. W.; Schlingmann, K. P. (2011). „Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects”. Pediatric Nephrology. 26 (10): 1789—802. PMC 3163795 . PMID 21503667. doi:10.1007/s00467-011-1871-4.
- Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F (2006). „Type IV Bartter syndrome: report of two new cases”. Pediatr. Nephrol. 21 (6): 766—70. PMID 16583241. doi:10.1007/s00467-006-0090-x.
- Nakhoul, F; Nakhoul, N; Dorman, E; Berger, L; Skorecki, K; Magen, D (фебруар 2012). „"Gitelman's syndrome: a pathophysiological and clinical update"”. Endocrine (Review). 41 (1): 53—7. PMID 22169961. doi:10.1007/s12020-011-9556-0..
- Adachi M, Asakura Y, Sato Y, Tajima T, Nakajima T, Yamamoto T; et al. (2007). „Novel SLC12A1 (NKCC2) mutations in two families with Bartter syndrome type 1”. Endocr J. 54 (6): 1003—7. PMID 17998760. doi:10.1507/endocrj.K06-204..
- Aoi N, Nakayama T, Tahira Y, Haketa A, Yabuki M, Sekiyama T; et al. (април 2007). „Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome.”. Endocrine. 31 (2): 149—53. PMID 17873326. doi:10.1007/s12020-007-0024-9..
- Al Shibli A, Narchi H (2015). „Bartter and Gitelman syndromes: Spectrum ofclinical manifestations caused by different mutations.”. World J Methodol. 5 (2): 55—61. PMC 4482822 . PMID 26140272. doi:10.5662/wjm.v5.i2.55 ..
- Simon, D. B.; Karet, F. E.; Rodriguez-Soriano, J.; Hamdan, J. H.; DiPietro, A.; et al. (октобар 1996). „Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.”. Nat Genet. 14 (2): 152—6. PMID 8841184. doi:10.1038/ng1096-152..
- Simon, D. B.; Nelson-Williams, C.; Bia, M. J.; Ellison, D; Karet, F. E.; Molina, A. M.; et al. (јануар 1996). „Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.”. Nat Genet. 12 (1): 24—30. PMID 8528245. doi:10.1038/ng0196-24..
nih.gov (Global: 4th place; Serbian: 8th place)
ncbi.nlm.nih.gov
- Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP (јануар 1996). „Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.”. Nat. Genet. 12 (1): 24—30. PMID 8528245. doi:10.1038/ng0196-24.
- Rodriguez-Soriano J (1998). „Bartter and related sundromes: the puzzle is almost solved”. Pediatric Nephrology. 12 (4): 315—27. PMID 9655365. doi:10.1007/s004670050461..
- Bartter, F. C.; Pronove, P; Gill JR i sur (1962). „Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome”. The American Journal of Medicine. 33: 811—328. PMID 13969763. doi:10.1016/0002-9343(62)90214-0..
- Al Shibli A, Narchi H (2015). „Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations”. World J Methodol. 5 (2): 55—61. PMC 4482822 . PMID 26140272. doi:10.5662/wjm.v5.i2.55 ..
- Shaer, A. J. (2001). „Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes”. The American Journal of the Medical Sciences. 322 (6): 316—32. PMID 11780689. doi:10.1097/00000441-200112000-00004.
- Mastroianni N, De Fusco M, Zollo M, Arrigo G, Zuffardi O, Bettinelli A, Ballabio A, Casari G (август 1996). „"Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)"”. Genomics. 35 (3): 486—93. PMID 8812482. doi:10.1006/geno.1996.0388..
- Naesens M, Steels P, Verberckmoes R, Vanrenterghem Y, Kuypers D (2004). „Bartter's and Gitelman's syndromes: from gene to clinic”. Nephron Physiol. 96 (3): 65—78. PMID 15056980. doi:10.1159/000076752.
- Seyberth, H. W.; Schlingmann, K. P. (2011). „Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects”. Pediatric Nephrology. 26 (10): 1789—802. PMC 3163795 . PMID 21503667. doi:10.1007/s00467-011-1871-4.
- Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F (2006). „Type IV Bartter syndrome: report of two new cases”. Pediatr. Nephrol. 21 (6): 766—70. PMID 16583241. doi:10.1007/s00467-006-0090-x.
- Vezzoli, G.; Arcidiacono, T.; Paloschi, V. (2006). „Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome”. Journal of Nephrology. 19 (4): 525—8. PMID 17048213.
- Nakhoul, F; Nakhoul, N; Dorman, E; Berger, L; Skorecki, K; Magen, D (фебруар 2012). „"Gitelman's syndrome: a pathophysiological and clinical update"”. Endocrine (Review). 41 (1): 53—7. PMID 22169961. doi:10.1007/s12020-011-9556-0..
- Adachi M, Asakura Y, Sato Y, Tajima T, Nakajima T, Yamamoto T; et al. (2007). „Novel SLC12A1 (NKCC2) mutations in two families with Bartter syndrome type 1”. Endocr J. 54 (6): 1003—7. PMID 17998760. doi:10.1507/endocrj.K06-204..
- Aoi N, Nakayama T, Tahira Y, Haketa A, Yabuki M, Sekiyama T; et al. (април 2007). „Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome.”. Endocrine. 31 (2): 149—53. PMID 17873326. doi:10.1007/s12020-007-0024-9..
- Al Shibli A, Narchi H (2015). „Bartter and Gitelman syndromes: Spectrum ofclinical manifestations caused by different mutations.”. World J Methodol. 5 (2): 55—61. PMC 4482822 . PMID 26140272. doi:10.5662/wjm.v5.i2.55 ..
- Simon, D. B.; Karet, F. E.; Rodriguez-Soriano, J.; Hamdan, J. H.; DiPietro, A.; et al. (октобар 1996). „Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.”. Nat Genet. 14 (2): 152—6. PMID 8841184. doi:10.1038/ng1096-152..
- Simon, D. B.; Nelson-Williams, C.; Bia, M. J.; Ellison, D; Karet, F. E.; Molina, A. M.; et al. (јануар 1996). „Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.”. Nat Genet. 12 (1): 24—30. PMID 8528245. doi:10.1038/ng0196-24..
whonamedit.com (Global: 2,888th place; Serbian: 3,693rd place)
- „Gitelman's syndrome”. Whonamedit? - A dictionary of medical eponyms. Приступљено 26. 3. 2017.