Бартеров синдром (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Бартеров синдром" in Serbian language version.
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archive.org
- Bartter, P. C.; Pronove, P; Gill JR Jr, MacCardle RC (1962). „Hyperplasioa of juxtaglomerular complex with hyperaldosteronisam and hypokalemic alkalosis”. The American Journal of Medicine. 33: 811—28. PMID 13969763. doi:10.1016/0002-9343(62)90214-0.
- Mersin, S. S.; Rimelli, G. P.; Laux-End, R.; Bianchett, M. G. (1995). „Urinary chlorideexcretion distinguishes between renal and extrarenal metabolic alkalosis”. Eur J Pediatr. 154 (12): 979—82. PMID 8801106. doi:10.1007/BF01958641..
- Rodriguez Pereira R, Hasaart T (1982). „Hydramnion and observations inBartter's syndrome”. Acta Obstet Gynecol Scand. 61 (5): 477—8. PMID 6760656. doi:10.3109/00016348209156594..
doi.org
- Castrop, Hayo; Schießl, Ina Maria (2014-09-03). „Physiology and pathophysiology of the renal Na-K-2Cl cotransporter (NKCC2)”. American Journal of Physiology-Renal Physiology. 307 (9): F991—F1002. ISSN 1931-857X. PMID 25186299. doi:10.1152/ajprenal.00432.2014.
- Bartter, P. C.; Pronove, P; Gill JR Jr, MacCardle RC (1962). „Hyperplasioa of juxtaglomerular complex with hyperaldosteronisam and hypokalemic alkalosis”. The American Journal of Medicine. 33: 811—28. PMID 13969763. doi:10.1016/0002-9343(62)90214-0.
- Clive, D. M. (1985). „Bartter's syndrome: The unsolved puzzle”. Am J Kidney Dis. 25 (6): 813—23. PMID 7771476. doi:10.1016/0272-6386(95)90562-6..
- Proesmans, W. (2006). „Threading through the mizmaze of Bartter syndrome”. Pediatr. Nephrol. 21 (7): 896—902. PMID 16773399. S2CID 26270693. doi:10.1007/s00467-006-0113-7.
- Madrigal G, Saborio P, Mora F, Rincon G, Guay-Woodford LM (јун 1997). „Bartter syndrome in Costa Rica: a description of 20 cases”. Pediatric Nephrology. 11 (3): 296—301. PMID 9203176. doi:10.1007/s004670050280..
- Abdel-al YK, Badawi MH, Yaeesh SA, Habib YQ, al-Khuffash FA, al-Ghanim MM; et al. (јун 1999). „Bartter's syndrome in Arabic children: review of 13 cases”. Pediatr Int. 41 (3): 299—303. PMID 10365582. doi:10.1046/j.1442-200x.1999.01056.x..
- Rudin A. Bartter's syndrome. „A review of 28 patients followed for 10 years”. Acta Med Scand. 224 (2): 165—71. 1988. doi:10.1111/j.0954-6820.1988.tb16755.x..
- Fallen, K.; Banerjee, S.; Sheehan, J.; et al. (2009 Jan-Feb). „The Kir channel immunoglobulin domain is essential for Kir1.1 (ROMK) thermodynamic stability, trafficking and gating”. Channels (Austin). 3 (1): 57—68. PMC 7968143
. PMID 19221509. doi:10.4161/chan.3.1.7817. Проверите вредност парамет(а)ра за датум: |date=(помоћ). - Dane B, Dane C, Aksoy F, Cetin A, Yayla M (2010). „Antenatal Bartter syndrome: analysis of two cases with placental findings”. Fetal Pediatr Pathol. 29 (3): 121—6. PMID 20450264. doi:10.3109/15513811003777276..
- Rodríguez-Soriano, Juan (1998). „Bartter and related syndromes: The puzzle is almost solved”. Pediatric Nephrology. 12 (4): 315—327. PMID 9655365. S2CID 41782906. doi:10.1007/s004670050461.
- Knoers, Nine V.A.M.; Bindels, René J. (2016). „MAGE-D2 and the Regulation of Renal Salt Transporters”. New England Journal of Medicine. 374 (19): 1888—1890. PMID 27168439. S2CID 31460247. doi:10.1056/NEJMe1603856. hdl:1874/336856.
- Mersin, S. S.; Rimelli, G. P.; Laux-End, R.; Bianchett, M. G. (1995). „Urinary chlorideexcretion distinguishes between renal and extrarenal metabolic alkalosis”. Eur J Pediatr. 154 (12): 979—82. PMID 8801106. doi:10.1007/BF01958641..
- D’Avanzo M, Santinelli R, Tolone C et all (1995). „Concealed adiministrationof furosemide simulating Bartter syndrome in a 4,5-year-old boy”. Pediatr Nephroh. 9 (6): 749—50. PMID 8747119. doi:10.1007/BF00868731..
- Rodriguez Pereira R, Hasaart T (1982). „Hydramnion and observations inBartter's syndrome”. Acta Obstet Gynecol Scand. 61 (5): 477—8. PMID 6760656. doi:10.3109/00016348209156594..
- Ohlsson A, Sieck U, Cumming W, Akhtar M, Serenius F (1984). „A variant ofBartter's syndrome. Bartter's syndrome associated with hydramnio,prematurity, hypercalciuria and nephrocalcinosis”. Acta Paediatr Scan. 73 (6): 868—74. PMID 6395627. doi:10.1111/j.1651-2227.1984.tb17793.x..
- Seyberth, H. W. (2008). „An improved terminology and classification of Bartter-like syndromes”. Nat Clin Pract Nephrol. 4 (10): 560—7. PMID 18695706. doi:10.1038/ncpneph0912..
- Hegde, Deeparaj; Mondkar, Jayashree; Abdagire, Nitinkumar (2017-09-01). „Neonatal bartter syndrome in an extremely low birth weight baby”. Saudi Journal of Kidney Diseases and Transplantation (на језику: енглески). 28 (5): 1162—1164. ISSN 1319-2442. PMID 28937079. doi:10.4103/1319-2442.215121 .
- 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..
- Simon, David B.; Nelson-Williams, Carol; Johnson Bia, Margaret; Ellison, David; Karet, Fiona E.; Morey Molina, Antonio; Vaara, Ivar; Iwata, Fujihiko; Cushner, Howard M.; Koolen, Marianne; Gainza, Francisco J.; Gitelman, Hillel J.; Lifton, Richard P. (1996). „Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter”. Nature Genetics. 12 (1): 24—30. PMID 8528245. S2CID 1547909. doi:10.1038/ng0196-24..
- Fremont, O. T.; Chan, J. C. (2012). „Understanding Bartter syndrome and Gitelman syndrome”. World J Pediatr. 8: 25—30. doi:10.1007/s12519-012-0333-9.
- 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. S2CID 34031819. doi:10.1007/s00467-006-0090-x.
- Proesmans W, Massa G, Vanderberghe K, Assache AV (1987). „Prenatal diagnosisin Bartter suyndrome”. Lancet. 1 (8529): 394. PMID 2880209. doi:10.1016/S0140-6736(87)91781-8..
- Dane B, Yayla M, Dane C, Cetin A (2007). „Prenatal diagnosis of Bartter syndrome with biochemical examination of amniotic fluid: Case report”. Fetal Diagn Ther. 22 (3): 206—8. PMID 17228161. doi:10.1159/000098719..
- Kaplan, B. S.; Resiano, I; Raual, D. S.; Gottlieb RP; Bernstein, J. (1994). „Renal failurein the neonate associated with in utero exposure to nesteroidal anti-inflamatoryagens”. Pediatric Nephrology. 8: 700—4. doi:10.1007/BF00869093..
- Marlow, N.; Chiswick, M. L. (1982). „Neonatal Bartter's syndrome, indometacinand necrotizing enterocolitis”. Acta Paediatr Scand. 1 (6): 1031—2. PMID 7158325. doi:10.1111/j.1651-2227.1982.tb09569.x..
- 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 ..
- 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.
- 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 FE; Molina AM; 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..
- Ataoglu, E.; Civilibal, M.; Ozkul, A. A.; et al. (2009). „Indomethacin-induced colon perforation in Bartter's syndrome.”. Indian J Pediatr. 76 (3): 322—3. PMID 19347676. doi:10.1007/s12098-009-0062-9.
handle.net
hdl.handle.net
- Knoers, Nine V.A.M.; Bindels, René J. (2016). „MAGE-D2 and the Regulation of Renal Salt Transporters”. New England Journal of Medicine. 374 (19): 1888—1890. PMID 27168439. S2CID 31460247. doi:10.1056/NEJMe1603856. hdl:1874/336856.
lecturio.com
- „Bartter Syndrome”. The Lecturio Medical Concept Library. Приступљено 3. 7. 2021.
merckmanuals.com
- „Bartter Syndrome and Gitelman Syndrome - Children's Health Issues”. Merck Manuals Consumer Version (на језику: енглески). Приступљено 16. 1. 2021.
nih.gov
ncbi.nlm.nih.gov
- Castrop, Hayo; Schießl, Ina Maria (2014-09-03). „Physiology and pathophysiology of the renal Na-K-2Cl cotransporter (NKCC2)”. American Journal of Physiology-Renal Physiology. 307 (9): F991—F1002. ISSN 1931-857X. PMID 25186299. doi:10.1152/ajprenal.00432.2014.
- Bartter, P. C.; Pronove, P; Gill JR Jr, MacCardle RC (1962). „Hyperplasioa of juxtaglomerular complex with hyperaldosteronisam and hypokalemic alkalosis”. The American Journal of Medicine. 33: 811—28. PMID 13969763. doi:10.1016/0002-9343(62)90214-0.
- Clive, D. M. (1985). „Bartter's syndrome: The unsolved puzzle”. Am J Kidney Dis. 25 (6): 813—23. PMID 7771476. doi:10.1016/0272-6386(95)90562-6..
- Proesmans, W. (2006). „Threading through the mizmaze of Bartter syndrome”. Pediatr. Nephrol. 21 (7): 896—902. PMID 16773399. S2CID 26270693. doi:10.1007/s00467-006-0113-7.
- Madrigal G, Saborio P, Mora F, Rincon G, Guay-Woodford LM (јун 1997). „Bartter syndrome in Costa Rica: a description of 20 cases”. Pediatric Nephrology. 11 (3): 296—301. PMID 9203176. doi:10.1007/s004670050280..
- Abdel-al YK, Badawi MH, Yaeesh SA, Habib YQ, al-Khuffash FA, al-Ghanim MM; et al. (јун 1999). „Bartter's syndrome in Arabic children: review of 13 cases”. Pediatr Int. 41 (3): 299—303. PMID 10365582. doi:10.1046/j.1442-200x.1999.01056.x..
- Fallen, K.; Banerjee, S.; Sheehan, J.; et al. (2009 Jan-Feb). „The Kir channel immunoglobulin domain is essential for Kir1.1 (ROMK) thermodynamic stability, trafficking and gating”. Channels (Austin). 3 (1): 57—68. PMC 7968143 . PMID 19221509. doi:10.4161/chan.3.1.7817. Проверите вредност парамет(а)ра за датум:
|date=(помоћ). - Dane B, Dane C, Aksoy F, Cetin A, Yayla M (2010). „Antenatal Bartter syndrome: analysis of two cases with placental findings”. Fetal Pediatr Pathol. 29 (3): 121—6. PMID 20450264. doi:10.3109/15513811003777276..
- Rodríguez-Soriano, Juan (1998). „Bartter and related syndromes: The puzzle is almost solved”. Pediatric Nephrology. 12 (4): 315—327. PMID 9655365. S2CID 41782906. doi:10.1007/s004670050461.
- Knoers, Nine V.A.M.; Bindels, René J. (2016). „MAGE-D2 and the Regulation of Renal Salt Transporters”. New England Journal of Medicine. 374 (19): 1888—1890. PMID 27168439. S2CID 31460247. doi:10.1056/NEJMe1603856. hdl:1874/336856.
- McCredie, D. A. (1996). „Variants of Bartter's syndrome”. Pediatric Nephrology. 10 (4): 419—21. PMID 8865235.
- Mersin, S. S.; Rimelli, G. P.; Laux-End, R.; Bianchett, M. G. (1995). „Urinary chlorideexcretion distinguishes between renal and extrarenal metabolic alkalosis”. Eur J Pediatr. 154 (12): 979—82. PMID 8801106. doi:10.1007/BF01958641..
- D’Avanzo M, Santinelli R, Tolone C et all (1995). „Concealed adiministrationof furosemide simulating Bartter syndrome in a 4,5-year-old boy”. Pediatr Nephroh. 9 (6): 749—50. PMID 8747119. doi:10.1007/BF00868731..
- Gitelman, H. J.; Graham, J. B.; Welt, L. G. (1966). „A new familial disorder characterized by hypokalemia and hypomagnesemia”. Trans Assoc Am Physicians. 79: 221—3. PMID 5929460..
- Rodriguez Pereira R, Hasaart T (1982). „Hydramnion and observations inBartter's syndrome”. Acta Obstet Gynecol Scand. 61 (5): 477—8. PMID 6760656. doi:10.3109/00016348209156594..
- Ohlsson A, Sieck U, Cumming W, Akhtar M, Serenius F (1984). „A variant ofBartter's syndrome. Bartter's syndrome associated with hydramnio,prematurity, hypercalciuria and nephrocalcinosis”. Acta Paediatr Scan. 73 (6): 868—74. PMID 6395627. doi:10.1111/j.1651-2227.1984.tb17793.x..
- Seyberth, H. W. (2008). „An improved terminology and classification of Bartter-like syndromes”. Nat Clin Pract Nephrol. 4 (10): 560—7. PMID 18695706. doi:10.1038/ncpneph0912..
- Hegde, Deeparaj; Mondkar, Jayashree; Abdagire, Nitinkumar (2017-09-01). „Neonatal bartter syndrome in an extremely low birth weight baby”. Saudi Journal of Kidney Diseases and Transplantation (на језику: енглески). 28 (5): 1162—1164. ISSN 1319-2442. PMID 28937079. doi:10.4103/1319-2442.215121 .
- Kumar, P. S.; Deenadayalan, M; Janakiraman, L.; Vijayakumar, M. (2006). „Neonatal Bartter syndrome”. Indian Pediatr. 43 (8): 735—7. PMID 16951440..
- 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..
- Simon, David B.; Nelson-Williams, Carol; Johnson Bia, Margaret; Ellison, David; Karet, Fiona E.; Morey Molina, Antonio; Vaara, Ivar; Iwata, Fujihiko; Cushner, Howard M.; Koolen, Marianne; Gainza, Francisco J.; Gitelman, Hillel J.; Lifton, Richard P. (1996). „Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter”. Nature Genetics. 12 (1): 24—30. PMID 8528245. S2CID 1547909. doi:10.1038/ng0196-24..
- 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. S2CID 34031819. 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.
- Proesmans W, Massa G, Vanderberghe K, Assache AV (1987). „Prenatal diagnosisin Bartter suyndrome”. Lancet. 1 (8529): 394. PMID 2880209. doi:10.1016/S0140-6736(87)91781-8..
- Dane B, Yayla M, Dane C, Cetin A (2007). „Prenatal diagnosis of Bartter syndrome with biochemical examination of amniotic fluid: Case report”. Fetal Diagn Ther. 22 (3): 206—8. PMID 17228161. doi:10.1159/000098719..
- Marlow, N.; Chiswick, M. L. (1982). „Neonatal Bartter's syndrome, indometacinand necrotizing enterocolitis”. Acta Paediatr Scand. 1 (6): 1031—2. PMID 7158325. doi:10.1111/j.1651-2227.1982.tb09569.x..
- 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 ..
- 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.
- 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 FE; Molina AM; 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..
- Ataoglu, E.; Civilibal, M.; Ozkul, A. A.; et al. (2009). „Indomethacin-induced colon perforation in Bartter's syndrome.”. Indian J Pediatr. 76 (3): 322—3. PMID 19347676. doi:10.1007/s12098-009-0062-9.
physiology.org
journals.physiology.org
- Castrop, Hayo; Schießl, Ina Maria (2014-09-03). „Physiology and pathophysiology of the renal Na-K-2Cl cotransporter (NKCC2)”. American Journal of Physiology-Renal Physiology. 307 (9): F991—F1002. ISSN 1931-857X. PMID 25186299. doi:10.1152/ajprenal.00432.2014.
semanticscholar.org
api.semanticscholar.org
- Proesmans, W. (2006). „Threading through the mizmaze of Bartter syndrome”. Pediatr. Nephrol. 21 (7): 896—902. PMID 16773399. S2CID 26270693. doi:10.1007/s00467-006-0113-7.
- Rodríguez-Soriano, Juan (1998). „Bartter and related syndromes: The puzzle is almost solved”. Pediatric Nephrology. 12 (4): 315—327. PMID 9655365. S2CID 41782906. doi:10.1007/s004670050461.
- Knoers, Nine V.A.M.; Bindels, René J. (2016). „MAGE-D2 and the Regulation of Renal Salt Transporters”. New England Journal of Medicine. 374 (19): 1888—1890. PMID 27168439. S2CID 31460247. doi:10.1056/NEJMe1603856. hdl:1874/336856.
- Simon, David B.; Nelson-Williams, Carol; Johnson Bia, Margaret; Ellison, David; Karet, Fiona E.; Morey Molina, Antonio; Vaara, Ivar; Iwata, Fujihiko; Cushner, Howard M.; Koolen, Marianne; Gainza, Francisco J.; Gitelman, Hillel J.; Lifton, Richard P. (1996). „Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter”. Nature Genetics. 12 (1): 24—30. PMID 8528245. S2CID 1547909. doi:10.1038/ng0196-24..
- 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. S2CID 34031819. doi:10.1007/s00467-006-0090-x.
sjkdt.org
- Hegde, Deeparaj; Mondkar, Jayashree; Abdagire, Nitinkumar (2017-09-01). „Neonatal bartter syndrome in an extremely low birth weight baby”. Saudi Journal of Kidney Diseases and Transplantation (на језику: енглески). 28 (5): 1162—1164. ISSN 1319-2442. PMID 28937079. doi:10.4103/1319-2442.215121 .
whonamedit.com
- synd/2328 на сајту Who Named It
- „Bartter's syndrome”. www.whonamedit.com.
wikipedia.org
en.wikipedia.org
- Knoers, Nine V.A.M.; Bindels, René J. (2016). „MAGE-D2 and the Regulation of Renal Salt Transporters”. New England Journal of Medicine. 374 (19): 1888—1890. PMID 27168439. S2CID 31460247. doi:10.1056/NEJMe1603856. hdl:1874/336856.
worldcat.org
- Castrop, Hayo; Schießl, Ina Maria (2014-09-03). „Physiology and pathophysiology of the renal Na-K-2Cl cotransporter (NKCC2)”. American Journal of Physiology-Renal Physiology. 307 (9): F991—F1002. ISSN 1931-857X. PMID 25186299. doi:10.1152/ajprenal.00432.2014.
- Hegde, Deeparaj; Mondkar, Jayashree; Abdagire, Nitinkumar (2017-09-01). „Neonatal bartter syndrome in an extremely low birth weight baby”. Saudi Journal of Kidney Diseases and Transplantation (на језику: енглески). 28 (5): 1162—1164. ISSN 1319-2442. PMID 28937079. doi:10.4103/1319-2442.215121 .