Works matching DE "BARTTER syndrome"

Results: 202

Bartter-like syndrome in patients with molecular defects of the insulin receptor gene.

Published in:

2014

By:

Watanabe, Toru;
Abe, Yuki

Publication type:

Letter

Clinical Course and Prognosis of Tubulopathies Characterized by Metabolic Alkalosis in Children.

Published in:

Turkish Archives of Pediatrics, 2022, v. 57, n. 6, p. 644, doi. 10.5152/TurkArchPediatr.2022.22124

By:

Huseynli, Bahruz;
Atmış, Bahriye;
Cevizli, Derya;
Bişgin, Atıl;
Bayazıt, Aysun Karabay

Publication type:

Article

Effective medical treatment strategies to help cessation of purging behaviors.

Published in:

International Journal of Eating Disorders, 2016, v. 49, n. 3, p. 324, doi. 10.1002/eat.22500

By:

Mascolo, Margherita;
McBride, Jennifer;
Mehler, Philip S.

Publication type:

Article

What the emergency department needs to know when caring for your patients with eating disorders.

Published in:

International Journal of Eating Disorders, 2012, v. 45, n. 8, p. 977, doi. 10.1002/eat.22035

By:

Mascolo, Margherita;
Trent, Stacy;
Colwell, Christopher;
Mehler, Philip S.

Publication type:

Article

Molecular Genetics of Bartter Syndrome.

Published in:

Journal of Pediatric Nephrology, 2014, v. 2, n. 1, p. 6

By:

Fazilaty, Hassan;
Behnam, Babak

Publication type:

Article

P10.01: Bartter syndrome: a rare cause of refractory severe polyhydramnios.

Published in:

Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 185, doi. 10.1002/uog.18095

By:

Fatma, A.;
Ali, F.;
Alberry, M.

Publication type:

Article

P10.02: Idiopathic polyhydramnios and antenatal Bartter syndrome: diagnostic criteria?

Published in:

Ultrasound in Obstetrics & Gynecology, 2017, v. 50, p. 185, doi. 10.1002/uog.18096

By:

Rule, T.;
Thomas, J.;
Petersen, S.G.;
Marshall, G.;
Kumar, S.;
Gardener, G.

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

Prenatal presentation of transient central diabetes insipidus.

Published in:

2011

By:

Kollamparambil, Tanoj Gopalan;
Mohan, Pammi Venkatesh;
Gunasuntharam, Kavitha;
Jani, Bhavdeep Rameshchandra;
Penma, David Gerard;
Penman, David Gerard

Publication type:

journal article

Bartter's syndrome results from an imbalance of vasoactive hormones.

Published in:

1977

By:

McGiff, John C.;
McGiff, J C

Publication type:

journal article

Bartter's syndrome: urinary prostaglandin E-like material and kallikrein; indomethacin effects.

Published in:

1977

By:

Halushka, Perry V.;
Wohltmann, Hulda;
Privitera, Philip J.;
Hurwitz, Gilbert;
Margolius, Harry S.;
Halushka, P V;
Wohltmann, H;
Privitera, P J;
Hurwitz, G;
Margolius, H S

Publication type:

journal 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

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

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

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

Care of the Hospitalized Patient with Severe Anorexia Nervosa or Avoidant Restrictive Food Intake Disorder.

Published in:

MEDSURG Nursing, 2021, v. 30, n. 3, p. 197, doi. 10.62116/msj.2021.30.3.197

By:

Hovde, Krista;
Markovchick, Tasha;
Netzky, Julie;
Sandberg, Hannah;
Mehler, Philip S.

Publication type:

Article

Treating hearing loss in patients with infantile bartter syndrome.

Published in:

Laryngoscope, 2012, v. 122, n. 11, p. 2524, doi. 10.1002/lary.23532

By:

Kontorinis, Georgios;
Giesemann, Anja M.;
Iliodromiti, Zoe;
Weidemann, Juergen;
Aljeraisi, Talal;
Schwab, Burkard

Publication type:

Article

Treatment of Bartter syndrome. Unsolved issue.

Published in:

Jornal de Pediatria, 2014, v. 90, n. 5, p. 512, doi. 10.1016/j.jped.2014.01.012

By:

Pena Nascimento, Carla Lessa;
Garcia, Cecilia Lopes;
Soares Schvartsman, Benita Galassi;
Vaisbich, Maria Helena

Publication type:

Article

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

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

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

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

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

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

Correction of hypokalemia with antialdosterone therapy in Gitelman's syndrome.

Published in:

1994

By:

Colussi, Giacomo;
Rombolà, Giuseppe;
De Ferrari, Maria Elisabetta;
Macaluso, Margherita;
Minetti, Luigi;
Colussi, G;
Rombolà, G;
De Ferrari, M E;
Macaluso, M;
Minetti, L

Publication type:

journal article

Distal nephron function in Bartter's syndrome: abnormal conductance to chloride in the cortical collecting tubule?

Published in:

1992

By:

Colussi, Giacomo;
Rombolà, Giuseppe;
Verde, Giorgio;
Airaghi, Cristina;
Loli, Paola;
Minetti, Luigi;
Colussi, G;
Rombolà, G;
Verde, G;
Airaghi, C;
Loli, P;
Minetti, L

Publication type:

journal article

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

Does defective chloride reabsorption at the loop of Henle play a major role in the pathogenesis of Bartter's syndrome?

Published in:

1987

By:

Milani, L.;
Pessina, A.C.;
Maccà, F.;
Pauletto, P.;
Gatta, A.;
Maccà, F

Publication type:

journal article

A Case of Bartter's Syndrome Presenting in Adulthood.

Published in:

2020

By:

Yaqub, Sonia;
Arif, Muhammad Sohaib

Publication type:

journal article

Association of Mucopolysaccharidosis Type 4A and Bartter Syndrome.

Published in:

2019

By:

Soylu Ustkoyuncu, Pembe;
Nalcacioglu, Hulya;
Bastug, Funda;
Yel, Sibel;
Altuner Torun, Yasemin

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

Hypomagnesemia: An Evidence-Based Approach to Clinical Cases.

Published in:

Iranian Journal of Kidney Diseases, 2010, v. 4, n. 1, p. 13

By:

Assadi, Farahnak

Publication type:

Article

Molecular diagnostic results of a nephropathy gene panel in patients with suspected hereditary kidney disease.

Published in:

Laboratory Medicine, 2024, v. 55, n. 1, p. 13, doi. 10.1093/labmed/lmad027

By:

Topak, Ali

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

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

Bartter's syndrome: A rare cause of seizures and quadriparesis.

Published in:

2017

By:

Verma, Rajesh;
Qavi, Abdul;
Pandey, Sudhakar;
Bansod, Amrit A.

Publication type:

Case Study

Pediatric Tubular and Inherited Disorders in Asia: Results of Preliminary Survey of the Asian Pediatric Nephrology Association (AsPNA) Tubular and Inherited Working Group.

Published in:

Asian Journal of Pediatric Nephrology, 2022, v. 5, n. 1, p. 14, doi. 10.4103/ajpn.ajpn_2_22

By:

Real Resontoc, Lourdes Paula;
Kandai, Nozu;
Hooman, Nakisa;
Vasudevan, Anil;
Jie Ding;
Hee Gyung Kang

Publication type:

Article

In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.

Published in:

Human Genetics, 2009, v. 126, n. 4, p. 533, doi. 10.1007/s00439-009-0697-7

By:

Nozu, Kandai;
Iijima, Kazumoto;
Kawai, Kazuo;
Nozu, Yoshimi;
Nishida, Atsushi;
Takeshima, Yasuhiro;
Xue Jun Fu;
Hashimura, Yuya;
Kaito, Hiroshi;
Nakanishi, Koichi;
Yoshikawa, Norishige;
Matsuo, Masafumi

Publication type:

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

A case to use "salt‐losing tubulopathy" instead of "Bartter/Gitelman syndrome".

Published in:

2020

By:

Miura, Kenichiro;
Hattori, Motoshi

Publication type:

Case Study

Inherited salt‐losing tubulopathy: An old condition but a new category of tubulopathy.

Published in:

Pediatrics International, 2020, v. 62, n. 4, p. 428, doi. 10.1111/ped.14089

By:

Nozu, Kandai;
Yamamura, Tomohiko;
Horinouchi, Tomoko;
Nagano, China;
Sakakibara, Nana;
Ishikura, Kenji;
Hamada, Riku;
Morisada, Naoya;
Iijima, Kazumoto

Publication type:

Article