Results 11 to 20 of about 54 (51)

Caracterización genética de 14 familias con síndrome de Bartter y Gitelman

Iatreia, 2010
Intro ducción: los síndromes de Bartter y Gitelman son enfermedades de tipo hereditario con reducción marcada del transporte de sales en el asa ascendente gruesa de henle, alcalosis metabólica hipokalemica e hipercalciuria.
Astrid Lorena Urbano, Lina Serna, Ana María García, Lina Betancur, Carlos Medina, Juan José Vanegas, Nicolás Pineda Trujillo   +6 more
doaj  

The impact of the correction of hyponatremia during hospital admission on the prognosis of SARS-CoV-2 infection. [PDF]

Med Clin (Engl Ed), 2022
de La Flor JC, Gomez-Berrocal A, Marschall A, Valga F, Linares T, Albarracin C, Ruiz E, Gallegos G, Gómez A, de Los Santos A, Rodeles M.   +10 more
europepmc   +2 more sources

Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3. [PDF]

Sci Rep, 2023
García-Castaño A, Gómez-Conde S, Gondra L, Herrero M, Aguirre M, de la Hoz AB, Castaño L, Renaltube group, Madariaga L.   +8 more
europepmc   +1 more source

Fe de errores de “Síndrome de pseudo-Bartter como presentación de fibrosis quística con mutación DF508”

Boletín Médico del Hospital Infantil de México, 2017
María de Jesús Galaviz-Ballesteros, Carlos Patricio Acosta-Rodríguez-Bueno, Alejandra Consuelo-Sánchez, Isidro Franco-Álvarez, Odilo Iván Olalla-Mera, Rodrigo Vázquez-Frias   +5 more
doaj   +1 more source

Adult presentation of Bartter syndrome type IV with erythrocytosis. [PDF]

Einstein (Sao Paulo), 2015
Heilberg IP, Tótoli C, Calado JT.
europepmc   +1 more source

Reduction in weight and cardiovascular disease risk factors in individuals with type 2 diabetes: one-year results of the look AHEAD trial. [PDF]

Diabetes Care, 2007
Look AHEAD Research Group, Pi-Sunyer X, Blackburn G, Brancati FL, Bray GA, Bright R, Clark JM, Curtis JM, Espeland MA, Foreyt JP, Graves K, Haffner SM, Harrison B, Hill JO, Horton ES, Jakicic J, Jeffery RW, Johnson KC, Kahn S, Kelley DE, Kitabchi AE, Knowler WC, Lewis CE, Maschak-Carey BJ, Montgomery B, Nathan DM, Patricio J, Peters A, Redmon JB, Reeves RS, Ryan DH, Safford M, Van Dorsten B, Wadden TA, Wagenknecht L, Wesche-Thobaben J, Wing RR, Yanovski SZ.   +37 more
europepmc   +1 more source

40 años de experiencia en síndrome de Bartter

Nefrología
Laura García Espinosa, Alejandro Zarauza Santoveña, Juan Bravo Feito, Marta Melgosa Hijosa, Carlota Fernández Camblor, Angel Alonso Melgar, Laura Espinosa Roman   +6 more
doaj   +1 more source

Adult-onset Bartter syndrome type IV B with ACTH secreting pituitary microadenoma. [PDF]

J Bras Nefrol
Mathew GG.
europepmc   +1 more source

[Ultrasound diagnosis of nephrocalcinosis in an infant with recurrent vomiting]. [PDF]

Aten Primaria
Carrasco Hidalgo-Barquero MC, Ortiz-Peces L, Ortiz-González L.   +2 more
europepmc   +1 more source

Nephrocalcinosis: unveiling renal tubulopathies in the genomic era. [PDF]

J Bras Nefrol
Ayoub EAM, Vaisbich MH, Rocha DR, Cerqueira BP, Matos ACC, Pietrobom IG, Heilberg IP.   +6 more
europepmc   +1 more source