Results 51 to 60 of about 385 (98)

Recuperación significativa del estado nutricional mediante manejo dietético individualizado en adolescente con desnutrición aguda severa y sospecha de síndrome de Gitelman: reporte de caso [PDF]

open access: yes
Introduction: Pediatric malnutrition is associated with growth delay and increased morbidity. Likewise, hereditary tubulopathies, often underdiagnosed due to their nonspecific presentation, are frequently accompanied by malnutrition as a relevant ...
Cuéllar Robles, Sofía   +2 more
core   +2 more sources

Impact of genetic mutations in hypokalemic periodic paralysis: Diagnosis and clinical management [PDF]

open access: yes
Neuromuscular diseases encompass a variety of disorders affecting muscular and nervous function, with numerous genetic conditions manifesting in diverse clinical forms.
Blacio Villa, Carlos Omar   +3 more
core   +2 more sources

Uma variante do gene WNK4 está associada à osteoporose mas não à hipertensão na população portuguesa [PDF]

open access: yes, 2011
Germline mutations in the WNK4 gene originate Gordon syndrome or pseudohypoaldosteronism type II, a familial form of hypertension with hyperkalemia and hypercalciuria.
Barbosa, A.P.   +7 more
core  

TFM PROFESIONAL Máster en Traducción Médico-Sanitaria 2013-2014 [PDF]

open access: yes, 2014
Treball Fi de Master: Màster Universitari en Traducció Medicosanitària.
López Sepúlveda, Marta
core  

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

open access: yesBoletín Médico del Hospital Infantil de México, 2017
María de Jesús Galaviz-Ballesteros   +5 more
doaj   +1 more source

Eficacia y seguridad del tolvaptán vs placebo en pacientes con hiponatremia asociada al síndrome de secreción inapropiada de hormona antidiurética (SIADH): Una Revisión sistemática y Metaanálisis [PDF]

open access: yes
Determinar si el tolvaptán es más eficaz y seguro que el placebo en incrementar los niveles de sodio en los pacientes con hiponatremia asociadas al síndrome de secreción inapropiada de hormona antidiurética (SIADH).
Zuñiga Baca, Dalmiro   +1 more
core  

40 años de experiencia en síndrome de Bartter

open access: yesNefrología
Laura García Espinosa   +6 more
doaj   +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]

open access: yesDiabetes Care, 2007
Look AHEAD Research Group   +37 more
europepmc   +1 more source

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

open access: yesAten Primaria
Carrasco Hidalgo-Barquero MC   +2 more
europepmc   +1 more source

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