Works matching Bartter syndrome

Results: 752

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.

Published in:

2019

By:

Najafi, Maryam;
Bakey, Zeineb;
Schmidts, Miriam;
Kordi-Tamandani, Dor Mohammad;
Behjati, Farkhondeh;
Sadeghi-Bojd, Simin;
Schüle, Isabel;
Karimiani, Ehsan Ghayoor;
Azarfar, Anoush

Publication type:

journal article

A Case of Antenatal Bartter Syndrome with Sensorineural Deafness.

Published in:

2010

By:

Lee, Hyun Seung;
Cheong, Hae Il;
Ki, Chang-Seok

Publication type:

Case Study

Bartter syndrome: A case report requiring emergency intervention.

Published in:

Ümraniye Pediatri Dergisi, 2024, v. 4, n. 2, p. 92, doi. 10.14744/upd.2024.38247

By:

Kutlu, Tuğba Nur;
Bozkurt, Hayrunnisa Bekis;
Ergüven, Müferet;
Bıçakcı, Zafer

Publication type:

Article

Chronic renal failure in a boy with classic Bartter's syndrome due to a novel mutation in CLCNKB coding for the chloride channel.

Published in:

2009

By:

Chien-Ming Lin;
Jeng-Daw Tsai;
Yi-Fen Lo;
Ming-Tso Yan;
Sung-Sen Yang;
Shih-Hua Lin;
Lin, Chien-Ming;
Tsai, Jeng-Daw;
Lo, Yi-Fen;
Yan, Ming-Tso;
Yang, Sung-Sen;
Lin, Shih-Hua

Publication type:

journal article

Congenital chloride diarrhea misdiagnosed as pseudo-Bartter syndrome.

Published in:

Journal of Research in Medical Sciences, 2013, v. 18, n. 9, p. 822

By:

Saneian, Hossein;
Bahraminia, Emad

Publication type:

Article

A novel variant in the SLC12A1 gene in two families with antenatal Bartter syndrome.

Published in:

2017

By:

Breinbjerg, Anders;
Siggaard Rittig, Charlotte;
Gregersen, Niels;
Rittig, Søren;
Hvarregaard Christensen, Jane

Publication type:

journal article

Neonates with Bartter syndrome have enormous fluid and sodium requirements.

Published in:

Acta Paediatrica, 2015, v. 104, n. 7, p. e294, doi. 10.1111/apa.12981

By:

Azzi, Antonio;
Chehade, Hassib;
Deschênes, Georges

Publication type:

Article

CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca dependence of ClC-Kb channels.

Published in:

Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 9, p. 1713, doi. 10.1007/s00424-013-1401-2

By:

Andrini, Olga;
Keck, Mathilde;
L'Hoste, Sébastien;
Briones, Rodolfo;
Mansour-Hendili, Lamisse;
Grand, Teddy;
Sepúlveda, Francisco;
Blanchard, Anne;
Lourdel, Stéphane;
Vargas-Poussou, Rosa;
Teulon, Jacques

Publication type:

Article

Neonatal Bartter Syndrome.

Published in:

Journal of Nepal Paediatric Society, 2016, v. 36, n. 2, p. 204, doi. 10.3126/jnps.v36i2.14818

By:

A., Roy;
D., Sarkar;
S., Dogra;
S., Sengupta

Publication type:

Article

A unique finding of normal aldosterone level in Bartter's syndrome.

Published in:

Journal of Nephropathology, 2017, v. 6, n. 4, p. 359, doi. 10.15171/jnp.2017.59

By:

Raina, Rupesh;
Chaturvedi, Tushar;
Polaconda, Shyam;
Mukunda, Amrita Siri;
Sethi, Sidharth Kumar;
Krishnappa, Vinod

Publication type:

Article

Status epilepticus as the only presentation of the neonatal Bartter syndrome.

Published in:

2012

By:

Patra, Soumya;
Konar, Mithun C.;
Basu, Rajarshi;
Khaowas, Ajoy K.;
Dutta, Soumyadeep;
Sarkar, Debanjali

Publication type:

Case Study

Bartter sendromlu hastada anestezi yaklaşımı: Olgu sunumu.

Published in:

Dicle Medical Journal / Dicle Tip Dergisi, 2012, v. 39, n. 3, p. 449, doi. 10.5798/diclemedj.0921.2012.03.0179

By:

Aydoğan, Harun;
Bilgiç, Tekin;
Karahan, Mahmut Alp;
Yalçın, Şaban

Publication type:

Article

Bartter syndrome-like phenotype in a patient with diabetes: a case report.

Published in:

2018

By:

Dalugama, Chamara;
Pathirage, Manoji;
Kularatne, S. A. M.

Publication type:

journal article

Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome.

Published in:

Clinical Genetics, 2010, v. 77, n. 2, p. 155, doi. 10.1111/j.1399-0004.2009.01288.x

By:

Yu, Y.;
Xu, C.;
Pan, X.;
Ren, H.;
Wang, W.;
Meng, X.;
Huang, F.;
Chen, N.

Publication type:

Article

Bartter Type 4a Syndrome Diagnosed in a 30-week-old Preterm Neonate.

Published in:

Bagcilar Medical Bulletin / Bağcılar Tıp Bülteni, 2023, v. 8, n. 1, p. 103, doi. 10.4274/BMB.galenos.2023.2022-12-103

By:

Gök, Çağrı Cumhur;
Kaynar, Özge;
Şentürk, Leyli;
Can, Emrah;
Hamilçıkan, Şahin

Publication type:

Article

Bartter Syndrome Represented by Recurrent Hypokalemia Attacks: A Case Report.

Published in:

2017

By:

Küçük, Nuran;
Kuzaytepe, Esra Çelik;
Esmi, Esma;
Dülger, Şerife;
Erkin, Gökşen

Publication type:

Case Study

Rare Presentation of Cystinosis Mimicking Bartter's Syndrome: Reports of Two Patients and Review of the Literature.

Published in:

Renal Failure, 2010, v. 32, n. 2, p. 277, doi. 10.3109/08860221003592804

By:

Çaltik, Aysun;
Akyüz, Sare Gülfem;
Erdogan, Özlem;
Bülbül, Mehmet;
Demircin, Gülay

Publication type:

Article

Acute kidney injury in type 3 Bartter syndrome: Angiotensin-converting enzyme inhibitors as a cause.

Published in:

Pediatrics International, 2016, v. 58, n. 12, p. 1373, doi. 10.1111/ped.13100

By:

Nagao, Ryuhei;
Suzuki, Shinzi;
Kawashima, Hisashi;
Nozu, Kandai;
Iijima, Kazumoto

Publication type:

Article

Bartter syndrome: causes, diagnosis, and treatment.

Published in:

International Journal of Nephrology & Renovascular Disease, 2018, v. 11, p. 291, doi. 10.2147/IJNRD.S155397

By:

Cunha, Tamara da Silva;
Heilberg, Ita Pfeferman

Publication type:

Article

A Case of Bartter's Syndrome Presenting in Adulthood.

Published in:

2020

By:

Yaqub, Sonia;
Arif, Muhammad Sohaib

Publication type:

journal article

Nephropathic Cystinosis Mimicking Bartter Syndrome: a Novel Mutation.

Published in:

2018

By:

Bastug, Funda;
Nalcacioglu, Hulya;
Ozaltin, Fatih;
Korkmaz, Emine;
Yel, Sibel

Publication type:

journal article

Anesthetic management of a patient with Bartter's syndrome undergoing bilateral sagittal split osteotomy.

Published in:

Saudi Journal of Anaesthesia, 2012, v. 6, n. 4, p. 419, doi. 10.4103/1658-354X.105895

By:

Nooh, Nasser;
Abdullah, Walid;
Sheta, Saad

Publication type:

Article

Cystinosis Presenting with Findings of Bartter Syndrome.

Published in:

2011

By:

Ozkan, Behzat;
Cay›r, Atilla;
Koflan, Celalettin;
Alp, Handan

Publication type:

Case Study

A Report of Two Patients with Food Protein-induced Enterocolitis Mimicking Bartter Syndrome.

Published in:

2021

By:

Darougar, Sepideh;
Shirzani, Arezoo;
Mansouri, Mahboubeh;
Mohkam, Masoumeh

Publication type:

journal article

Late-Onset Bartter's Syndrome Type II with End-Stage Renal Disease Due to a Novel Mutation in KCNJ1 Gene in an Indian Adult Male -- A Case Report.

Published in:

Indian Journal of Nephrology, 2023, v. 33, n. 1, p. 57, doi. 10.4103/ijn.ijn_383_21

By:

Gaggar, Payal;
D., Sree Bhushan Raju;
M., Ravi Tej;
Pragna, P.

Publication type:

Article

Association of Amelogenesis Imperfecta and Bartter's Syndrome.

Published in:

Indian Journal of Nephrology, 2017, v. 27, n. 5, p. 399, doi. 10.4103/ijn.IJN_203_16

By:

Kumar, A. C. V.;
Alekya, V.;
Krishna, M. S. V. V.;
Alekya, K.;
Aruna, M.;
Reddy, M. H. K.;
Sangeetha, B.;
Ram, R.;
Kumar, V. S.

Publication type:

Article

Neonatal Bartter syndrome associated with ileal atresia and cystic fibrosis.

Published in:

2013

By:

Akuma, A. O.;
Mittal, S. K.;
Sambo, A. A.

Publication type:

Case Study

Antenatal Bartter's syndrome with sensorineural deafness.

Published in:

Indian Journal of Nephrology, 2009, v. 19, n. 1, p. 23, doi. 10.4103/0971-4065.50677

By:

Bhamkar, R. P.;
Gajendragadkar, A.

Publication type:

Article

Long-term follow-up of patients with Bartter syndrome type I and II.

Published in:

Nephrology Dialysis Transplantation, 2010, v. 25, n. 9, p. 2976, doi. 10.1093/ndt/gfq119

By:

Puricelli, Elena;
Bettinelli, Alberto;
Borsa, Nicoló;
Sironi, Francesca;
Mattiello, Camilla;
Tammaro, Fabiana;
Tedeschi, Silvana;
Bianchetti, Mario G.

Publication type:

Article

Pseudo-Bartter syndrome and staghorn calculi in an infant with chronic diarrhea: Answers.

Published in:

2021

By:

Leventoğlu, Emre;
Büyükkaragöz, Bahar;
Düztaş, Demet Teker;
Gürkan, Ödül Eğritaş

Publication type:

Case Study

Pseudo-Bartter syndrome and staghorn calculi in an infant with chronic diarrhea: Questions.

Published in:

2021

By:

Leventoğlu, Emre;
Büyükkaragöz, Bahar;
Düztaş, Demet Teker;
Gürkan, Ödül Eğritaş

Publication type:

Case Study

Bartter syndrome and growth hormone deficiency: three cases.

Published in:

2012

By:

Buyukcelik, Mithat;
Keskin, Mehmet;
Kilic, Beltinge;
Kor, Yilmaz;
Balat, Ayse

Publication type:

Report

Different roles of the RAAS affect bone metabolism in patients with primary aldosteronism, Gitelman syndrome and Bartter syndrome.

Published in:

BMC Endocrine Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12902-022-00955-2

By:

Tang, Wangna;
Chai, Yun;
Jia, Hongwei;
Wang, Baoping;
Liu, Tong;
Wang, Hao;
Dai, Chenlin

Publication type:

Article

Colistin-induced Bartter-like Syndrome: Ponder before Treatment!

Published in:

Indian Journal of Critical Care Medicine, 2022, v. 26, n. 2, p. 239, doi. 10.5005/jp-journals-10071-24117

By:

Kumari, Anju;
Gupta, Poonam;
Verma, Himanshu;
Kumar, Ajay;
Thakur, Preeti;
Sharma, Kavish

Publication type:

Article

A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis.

Published in:

Clinical & Experimental Nephrology, 2010, v. 14, n. 3, p. 278, doi. 10.1007/s10157-009-0262-7

By:

Akil, Ipek;
Ozen, Serkan;
Kandiloglu, Ali Rizak;
Ersoy, Betul

Publication type:

Article

Cisplatin Therapy Does Not Worsen Renal Function in Severe Antenatal Bartter Syndrome.

Published in:

2017

By:

Welch, Thomas R.;
Shaffer, David R.;
Feldman, Darren R.

Publication type:

Case Study

Rare Variant of Bartter Syndrome with Sensorineural Deafness.

Published in:

2015

By:

R., Kumar;
P., Kumar;
M., Kumar

Publication type:

Case Study

Suppressed diluting segment reabsorption in Bartter's syndrome: studies in 1 patient and synthesis of literature data.

Published in:

1988

By:

Hené, Ronald J.;
Koomans, Hein A.;
Dorhout Mees, Evert J.;
Hené, R J;
Koomans, H A;
Mees, E J

Publication type:

journal article

Neonatal Bartter syndrome and unilateral ectopic renal cyst as new renal causes of hydrops fetalis: two case reports and review of the literature.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2013, v. 26, n. 11, p. 1147, doi. 10.3109/14767058.2013.783803

By:

Çetinkaya, Merih;
Durmaz, Oguzhan;
Büyükkale, Gökhan;
Ozbek, Sibel;
Acar, Deniz;
Kılıcaslan, Isın;
Kavuncuoglu, Sultan

Publication type:

Article

Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.

Published in:

Journal of Physiology, 2017, v. 595, n. 16, p. 5573, doi. 10.1113/JP274344

By:

Cheng, Chih‐Jen;
Lo, Yi‐Fen;
Chen, Jen‐Chi;
Huang, Chou‐Long;
Lin, Shih‐Hua

Publication type:

Article

BARTTER SYNDROME MIMICKING HYPOPITUITARISM.

Published in:

2013

By:

Korkmaz, H.;
Özkaya, M.;
Akarsu, E.;
Öztürk, Z. A.;
Koç, I.;
Araz, M.

Publication type:

Case Study

Classic Bartter syndrome complicated with profound growth hormone deficiency: a case report.

Published in:

2013

By:

Masanori Adachi;
Toshihiro Tajima;
Koji Muroya;
Yumi Asakura

Publication type:

Case Study

Contradiction between genetic analysis and diuretic loading test in type I Bartter syndrome: a case report.

Published in:

2021

By:

Kuroda, Jumpei;
Harada, Ryoko;
Hamada, Riku;
Okuda, Yusuke;
Yoshida, Yasuhiro;
Hataya, Hiroshi;
Nozu, Kandai;
Iijima, Kazumoto;
Honda, Masataka;
Ishikura, Kenji

Publication type:

journal article

Late-onset Bartter syndrome type II.

Published in:

Clinical Kidney Journal, 2017, v. 10, n. 5, p. 594, doi. 10.1093/ckj/sfx033

By:

Gollasch, Benjamin;
Anistan, Yoland-Marie;
Canaan-Kühl, Sima;
Gollasch, Maik

Publication type:

Article

Paradoxical hypertension and salt wasting in Type II Bartter syndrome.

Published in:

Clinical Kidney Journal, 2012, v. 5, n. 3, p. 217, doi. 10.1093/ckj/sfs026

By:

Chan, Winnie Kwai-yu;
To, Ka Fai;
Tong, Joanna H. M.;
Law, Chi Wai

Publication type:

Article

Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.

Published in:

2011

By:

Robitaille, Pierre;
Merouani, Aicha;
He, Ning;
Pei, York

Publication type:

journal article

Rectal Cancer in a Patient with Bartter Syndrome: A Case Report.

Published in:

2017

By:

Shiki Fujino;
Norikatsu Miyoshi;
Masayuki Ohue;
Mikio Mukai;
Yoji Kukita;
Taishi Hata;
Chu Matsuda;
Tsunekazu Mizushima;
Yuichiro Doki;
Masaki Mori

Publication type:

Case Study

ANTENATAL BARTTER SYNDROME: Analysis of Two Cases with Placental Findings.

Published in:

Fetal & Pediatric Pathology, 2010, v. 29, n. 3, p. 121, doi. 10.3109/15513811003777276

By:

Dane, Banu;
Dane, Cem;
Aksoy, Figen;
Cetin, Ahmet;
Yayla, Murat

Publication type:

Article

Acquired Bartter-like syndrome association with netilmicin therapy in an extremely low birth weight infant.

Published in:

Renal Failure, 2014, v. 36, n. 1, p. 123, doi. 10.3109/0886022X.2013.832861

By:

Sandal, Gonca;
Akbay, Şenay;
Ozen, Metehan

Publication type:

Article

Acquired Bartter-Like Syndrome Associated with Colistin Use in a Preterm Infant.

Published in:

Renal Failure, 2013, v. 35, n. 3, p. 411, doi. 10.3109/0886022X.2012.761084

By:

Cakir, Ufuk;
Alan, Serdar;
Zeybek, Cengiz;
Erdeve, Omer;
Atasay, Begum;
Yalcinkaya, Fatma;
Arsan, Saadet

Publication type:

Article