Results 111 to 120 of about 5,396 (203)

The Dietary Approach to the Treatment of the Rare Genetic Tubulopathies Gitelman’s and Bartter’s Syndromes [PDF]

, 2021
Francesco Francini, Laura Gobbi, Verdiana Ravarotto, S. Toniazzo, Federico Nalesso, Paolo Spinella, Lorenzo A. Calò   +6 more
openalex   +1 more source

Development of strategies for genetic diagnosis of hereditary glomerulopathies, tubulopathies and cystic kidney diseases by the sequencing sets of genes

, 2019
María Lara Besada Cerecedo, Noa Carrera Cachaza, María García Murias, Ana María Barcia de la Iglesia, Jorge Amigo Lechuga, Beatriz Sobrino Rey, Cándido Díaz Rodríguez, Miguel A. García-González   +7 more
openalex   +1 more source

Bartter Syndromes and Other Salt-Losing Tubulopathies [PDF]

, 2006
Robert Kleta, Detlef Böckenhauer
openalex   +1 more source

BARTTER SYNDROME: A RARE RENAL TUBULOPATHY

, 2021
Amelia Genunche‐Dumitrescu, Daniela Badea, Marius Cristian Marinaş, Daniela Neagoe, Tiberiu-Stefanita Tenea-Cojan, Aurelian-Adrian BADEA   +5 more
openalex   +1 more source

A Case of Hyperinsulinemic Hypoglycaemia Associated with Atypical Fanconi Renal Tubulopathy Syndrome Caused by an HNF4A Variant. [PDF]

Case Rep Nephrol Dial
Garriga-Edo S, Peris-Serra L, Ríos Duro H, Giralt M, Díaz-Troyano N, Ferrer R, Antolín Mate M, Pérez Dueñas B, Clemente M.   +8 more
europepmc   +1 more source

Light chain tubulopathy without Fanconi syndrome [PDF]

Nephrology Dialysis Transplantation, 2006
Samar M, Said, Adel M, Assaad, Jorge, Cerda, Samih H, Nasr   +3 more
openaire   +2 more sources

Chromogranin A-Associated Tubulopathy in a Patient With Neuroendocrine Tumor. [PDF]

Cureus
Sanborn M, Maity A, Limmonick V, Siddiqui A, Salvatore S, McHugh T.   +5 more
europepmc   +1 more source

Daratumumab-Based Regimen Significantly Induced Remission of Crystalline Light Chain Proximal Tubulopathy: A Case Report. [PDF]

Am J Case Rep
Zou X, Wang K, Zeng R.
europepmc   +1 more source

The diuretic‐ and Bartter‐like salt‐losing tubulopathies [PDF]

, 2000
Nikola Jeck, Martin Konrad, Melanie Hess, H. W. Seyberth   +3 more
openalex   +1 more source

Response to commentary on "Ultra-rare severe kidney dysplasia mimicking salt-wasting tubulopathy associated with TFCP2L1 gene variants". [PDF]

Pediatr Nephrol
Vaqueiro Graña M, Gómez-Conde S, Madariaga L.   +2 more
europepmc   +1 more source