Results 141 to 150 of about 6,243 (172)

An Unusual Presentation of Failure to Thrive in a Toddler: Bartter Syndrome. [PDF]

Cureus
R A, Upendra Bhatia S, Narayan K, Mohammed S, Yelkur P.   +4 more
europepmc   +1 more source

A Rare Case of Bartter Syndrome Type 3 Presenting With New-Onset Diabetes Mellitus. [PDF]

Cureus
Pradeep U, Acharya S, Kasat PR, Gupta A, Nehete T.   +4 more
europepmc   +1 more source

Congenital Nephrogenic Diabetes Insipidus Secondary to Antenatal Type IVa Bartter Syndrome. [PDF]

Sage Open Pediatr
Oweidat M, Alra'e M, Abdallah AJ, Alqam M, Rae Q, Talahmeh K, Hassouneh AWM.   +6 more
europepmc   +1 more source

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

Indian J Nephrol
Chowdhry R, Vaswani RK, David J.
europepmc   +1 more source

Case Report: Type II Bartter syndrome with a novel <i>KCNJ1</i> variant in a premature neonate presenting with features of salt-wasting congenital adrenal crisis and pseudo-hypoaldosteronism. [PDF]

Front Pediatr
Tsui HC, Cheng HT, Lam KY, Leung LT, Au KN, Wong WY, Siu LY, Wong LM.   +7 more
europepmc   +1 more source

Bartter Syndrome Presenting as Arginine-Vasopressin Resistance: A Report of 2 Cases. [PDF]

Am J Case Rep
Sousa M, Medeiros R, Rodrigues AL, Dias Pereira B.   +3 more
europepmc   +1 more source

Protein Quality Control of NKCC2 in Bartter Syndrome and Blood Pressure Regulation. [PDF]

Cells
Laghmani K.
europepmc   +1 more source

Bartter syndrome-like phenotype in a patient with type 2 diabetes mellitus. [PDF]

BMJ Case Rep
Kumar R, Shreshta N, Samdarshi S, Chauhan P.   +3 more
europepmc   +1 more source

Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome. [PDF]

BMC Med Genomics
Yan X, Hu Y, Zhang X, Gao X, Zhao Y, Peng H, Ouyang L, Zhang C.   +7 more
europepmc   +1 more source

Pseudo-Bartter syndrome as the initial presentation of cystic fibrosis in children: an important diagnosis not to be missed. [PDF]

BMJ Case Rep
Lopes CF, Almeida V, Gomes S, Cruz C.
europepmc   +1 more source