Results 161 to 170 of about 2,061,243 (253)

Successful treatment with two siblings affected classic Bartter syndrome [PDF]

, 2015
Nguyen Khanh, Vu Dung
core   +1 more source

Complexities of Bartter Syndrome Type III: A Case Study in Jordan. [PDF]

Oxf Med Case Reports
Hanifa H, Al-Badareen Y, Al-Refaai MM, Ganama NM, Alabrash MS, Alsaleh B.   +5 more
europepmc   +1 more source

Paradoxical Hyperkalemia in Bartter Syndrome: A Case Report of Severe Resistant Hyperkalemia Requiring Hemodialysis. [PDF]

Case Rep Nephrol
Vadher A, Zeb M, Joseph S, Kambhatla S, Saad C.   +4 more
europepmc   +1 more source

Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation. [PDF]

Clin Case Rep, 2022
Nojehdeh ST, Mojbafan M, Hooman N, Hoseini R, Otukesh H.   +4 more
europepmc   +1 more source

Endocrinology of the hypothalamus and the pituitary gland [PDF]

, 1973
Kuhlendahl, Hans, Scriba, Peter Christian   +1 more
core   +1 more source

A case of adult-onset Bartter syndrome with transient paraplegia. [PDF]

Oxf Med Case Reports
Siddiqui S, Irfan SA, Ahmed S, Baig MMA, Ahmed J, Iqbal J.   +5 more
europepmc   +1 more source

Coexistence of Neonatal Bartter Syndrome and Congenital Cutis Laxa, in which a new mutation in SLC12A1 was identified

, 2023
Fatih İşleyen, Dilek Ulubaş Işık, Sumru Kavurt, Ruslan Bayramov, Ahmet Yağmur Baş, Nihal Demirel   +5 more
openalex   +2 more sources

pH gating of ROMK (K _ir 1.1) channels: Control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome

, 1999
Uwe Schulte, Hartmut Hahn, Moira Konrad, Nikola Jeck, Christian Derst, K. Wild, Susanne Weidemann, J. P. Ruppersberg, B. Fakler, Jost Ludwig   +9 more
openalex   +2 more sources

Cochlear implantation in children with Bartter syndrome: A case report. [PDF]

Sci Prog
Badr KM, Raza SA, Alahmadi A, Alghamdi F, Thabet AM, Alghamdi S.   +5 more
europepmc   +1 more source

A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis. [PDF]

Mol Genet Genomic Med, 2022
Zhao Q, Xiang Q, Tan Y, Xiao X, Xie H, Wang H, Yang M, Liu S.   +7 more
europepmc   +1 more source