Works matching DE "BARTTER syndrome"

Results: 202

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

Genetic heterogeneity in patients with Bartter syndrome type 1.

Published in:

Molecular Medicine Reports, 2017, v. 15, n. 2, p. 581, doi. 10.3892/mmr.2016.6063

By:

Mingran Sun;
Jing Ning;
Weihong Xu;
Han Zhang;
Kaishu Zhao;
Wenfu Li;
Guiying Li;
Shibo Li

Publication type:

Article

Antenatal Bartter Syndrome: A Review.

Published in:

International Journal of Pediatrics, 2012, p. 1, doi. 10.1155/2012/857136

By:

Bhat, Y. Ramesh;
Vinayaka, G.;
Sreelakshmi, K.

Publication type:

Article

Pediatric Nephrology: Highlights for the General Practitioner.

Published in:

International Journal of Pediatrics, 2012, p. 1, doi. 10.1155/2012/270725

By:

Seikaly, Mouin;
Habib, Sabeen;
Barakat, Amin J.;
Gattineni, Jyothsna;
Quigley, Raymond;
Desi, Dev

Publication type:

Article

Classic Bartter syndrome complicated with profound growth hormone deficiency.

Published in:

2013

By:

Adachi, Masanori;
Tajima, Toshihiro;
Muroya, Koji;
Asakura, Yumi

Publication type:

Abstract

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

Hypokalaemia and failure to thrive: report of a misleading onset.

Published in:

Journal of Paediatrics & Child Health, 2010, v. 46, n. 5, p. 276, doi. 10.1111/j.1440-1754.2009.01684.x

By:

Conti, Giovanni;
Vitale, Agata;
Tedeschi, Silvana;
Syrén, Marie-Louise;
Pantano, Roberta;
Chimenz, Roberto;
Fede, Salvatore;
La Torre, Francesco;
Coviello, Domenico;
Fede, Carmelo

Publication type:

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

Does hypokalaemia cause nephropathy? an observational study of renal function in patients with Bartter or Gitelman syndrome.

Published in:

QJM: An International Journal of Medicine, 2011, v. 104, n. 11, p. 939, doi. 10.1093/qjmed/hcr095

By:

Walsh, S.B.;
Unwin, E.;
Vargas-Poussou, R.;
Houillier, P.;
Unwin, R.

Publication type:

Article

Inherited Renal Diseases.

Published in:

Current Pediatric Reviews, 2014, v. 10, n. 2, p. 95

By:

Leung, Jocelyn C.

Publication type:

Article

Whole Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death.

Published in:

2015

By:

CUTZ, ERNEST

Publication type:

Letter to the Editor

Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death.

Published in:

2015

By:

LOPEZ, HECTOR U.;
HAVERFIELD, EDEN;
CHUNG, WENDY K.

Publication type:

Case Study

Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.

Published in:

Nephrology Dialysis Transplantation, 2015, v. 30, n. 4, p. 621, doi. 10.1093/ndt/gfu362

By:

Corbetta, Samuele;
Raimondo, Francesca;
Tedeschi, Silvana;
Syrèn, Marie-Louise;
Rebora, Paola;
Savoia, Andrea;
Baldi, Lorenza;
Bettinelli, Alberto;
Pitto, Marina

Publication type:

Article

Paradoxical hypertension and salt wasting in Type II Bartter syndrome.

Published in:

Nephrology Dialysis Transplantation, 2012, v. 5, n. 3, p. 217

By:

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

Publication type:

Article

Genetic basis of Bartter syndrome in Korea.

Published in:

Nephrology Dialysis Transplantation, 2012, v. 27, n. 4, p. 1516, doi. 10.1093/ndt/gfr475

By:

Lee, Beom Hee;
Cho, Hee Yeon;
Lee, HyunKyung;
Han, Kyoung Hee;
Kang, Hee Gyung;
Ha, Il Soo;
Lee, Joo Hoon;
Park, Young Seo;
Shin, Jae Il;
Lee, Dae-Yeol;
Kim, Su-Yung;
Choi, Yong;
Cheong, Hae Il

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

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.

Published in:

Nephrology Dialysis Transplantation, 2009, v. 24, n. 5, p. 1455, doi. 10.1093/ndt/gfn689

By:

Karine Brochard;
Olivia Boyer;
Anne Blanchard;
Chantal Loirat;
Patrick Niaudet;
Marie-Alice Macher;
Georges Deschenes;
Albert Bensman;
Stéphane Decramer;
Pierre Cochat;
Denis Morin;
Françoise Broux;
Mathilde Caillez;
Claude Guyot;
Robert Novo;
Xavier Jeunemaître;
Rosa Vargas-Poussou

Publication type:

Article

Basic science in hypertension or diabetes.

Published in:: 2007
Publication type:: Abstract

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

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

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

A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 12, p. 866, doi. 10.1038/jhg.2011.110

By:

Ansar, Muhammad;
Lee, Kwanghyuk;
Naqvi, Syed Kamran-ul-Hassan;
Andrade, Paula B;
Basit, Sulman;
Santos-Cortez, Regie Lyn P;
Ahmad, Wasim;
Leal, Suzanne M

Publication type:

Article

Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes Insipidus.

Published in:

2018

By:

Vergine, Gianluca;
Fabbri, Elena;
Pedini, Annalisa;
Tedeschi, Silvana;
Borsa, Niccolò

Publication type:

Case Study

Potassium Channelopathies and Gastrointestinal Ulceration.

Published in:

Gut & Liver, 2016, v. 10, n. 6, p. 881, doi. 10.5009/gnl15414

By:

Jaeyong Han;
Seung Hun Lee;
Giebisch, Gerhard;
Tong Wang

Publication type:

Article

An infant with poor weight gain and hypochloremic metabolic alkalosis: a case report.

Published in:

2014

By:

Alhammadi, Ahmed H.;
Khalifa, Mohamed;
Alnaimi, Lolwa

Publication type:

Case Study

Parálisis hipocalémica en el embarazo: reporte de dos casos.

Published in:

2009

By:

Antonio Hernández Pacheco, José;
Estrada Altamirano, Ariel;
María Pérez Borbón, Guadalupe;
Torres Torres, Cutberto

Publication type:

Case Study

Childhood Bartter's syndrome: An Indian case series.

Published in:

2010

By:

Sampathkumar, K.;
Muralidharan, U.;
Kannan, A.;
Ramakrishnan, M.;
Ajeshkumar, R.

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

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

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

A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant.

Published in:

2019

By:

Arthuis, Chloé J.;
Winer, Norbert;
Nizon, Mathilde;
Isidor, Bertrand;
Kömhoff, Martin;
Riehmer, Vera;
Beck, Bodo B.;
Bihouée, Tiphaine;
Bruel, Alexandra;
Benbrik, Nadir

Publication type:

journal article

Early diagnosis of pseudo-Bartter syndrome in a hot climate region. Importance of suspecting the possibility of this diagnosis.

Published in:

Paediatria Croatica, 2014, v. 58, n. 2, p. 155, doi. 10.13112/pc.636

By:

Del Ciampo, Ieda Regina Lopes;
Sawamura, Regina;
Del Ciampo, Luiz Antonio;
Facincani, Inalda;
Machado Fernandes, Maria Inez

Publication type:

Article

The association of systemic oxidative stress with insulin resistance: mechanistic insights from studies in Bartter's and Gitelman's syndromes.

Published in:

2015

By:

Calò, Lorenzo A.;
Maiolino, Giuseppe;
Naso, Agostino;
Davis, Paul A.

Publication type:

Letter to the Editor

Reduced Membrane Insertion of CLC-K by V33L Barttin Results in Loss of Hearing, but Leaves Kidney Function Intact.

Published in:

Frontiers in Physiology, 2017, p. 1, doi. 10.3389/fphys.2017.00269

By:

Hua Tan;
Bungert-Plümke, Stefanie;
Fahlke, Christoph;
Stölting, Gabriel

Publication type:

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

Gitelman Syndrome in a Case of Diabetic Kidney Disease: A Diagnostic and Therapeutic Dilemma.

Published in:

Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 1, p. 19, doi. 10.7860/JCDR/2018/29991.11121

By:

SETH, VAIBHAV;
MANDAL, SOMNATH;
SARKAR, NILADRI;
NEOGI, SUBHASIS;
DAS, SHAMBADITYA

Publication type:

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

Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.

Published in:

PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173581

By:

García Castaño, Alejandro;
Pérez de Nanclares, Gustavo;
Madariaga, Leire;
Aguirre, Mireia;
Madrid, Álvaro;
Chocrón, Sara;
Nadal, Inmaculada;
Navarro, Mercedes;
Lucas, Elena;
Fijo, Julia;
Espino, Mar;
Espitaletta, Zilac;
García Nieto, Víctor;
Barajas de Frutos, David;
Loza, Reyner;
Pintos, Guillem;
Castaño, Luis;
Ariceta, Gema

Publication type:

Article

Hidden in Plain Sight--A Rare Presentation of Cystic Fibrosis with Pseudo-Bartter Syndrome.

Published in:

Indian Journal of Nephrology, 2024, v. 34, n. 5, p. 541, doi. 10.25259/ijn_53_23

By:

Chowdhry, Ratnapriya;
Vaswani, Rajwanti K;
David, Jane

Publication type:

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

Antenatal Bartter Syndrome Caused by a Novel Homozygous Mutation in SLC12A1 Gene.

Published in:

Indian Journal of Nephrology, 2019, v. 29, n. 5, p. 360, doi. 10.4103/ijn.IJN_175_18

By:

Acar, Filiz Aktürk;
Işik, Güneş;
Mutlu, Mehmet;
Kader, Şebnem;
Aslan, Yakup;
Kalyoncu, Mukaddes

Publication type:

Article

A case of adult onset barrter syndrome - A rare entity.

Published in:

Indian Journal of Nephrology, 2019, v. 29, n. 4, p. 302, doi. 10.4103/ijn.IJN_165_18

By:

Sehgal, Blessy;
Aggarwal, Rajesh;
Bhalla, Gaurav;
Aggarwal, Shalin

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

Gitelman syndrome in an infant.

Published in:

2015

By:

Nandi, M.;
Pandey, G.;
Sarkar, S.

Publication type:

Letter to the Editor

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

Bartter syndrome presenting as poor weight gain and dehydration in an infant.

Published in:

2012

By:

Alkhateeb, N. E. R.;
Gardee, Z. T.

Publication type:

Case Study

Adrenal venous sampling as a method of primary hyperaldosteronism assessment.

Published in:

Arterial Hypertension, 2023, v. 27, n. 3, p. 193, doi. 10.5603/ah.96381

By:

Giordano, Ugo;
Kobiałka, Jakub

Publication type:

Article

Unusual Complication of Multidrug Resistant Tuberculosis.

Published in:

2017

By:

Sharma, Prerna;
Sahay, Ravindra Nath

Publication type:

Case Study

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