Results 31 to 40 of about 62,890 (168)

Hiperpotasemia transitoria del lactante sin pérdida salina, enfoque fisiopatológico de tres casos

open access: yesNefrología, 2022
Resumen: Se reconocen 2 variedades de hiperpotasemia temprana de la infancia (del inglés Early childhood hyperkalemia) según la presencia o no de pérdida salina urinaria.
Caupolicán Alvarado   +5 more
doaj   +1 more source

Fatty Acid Oxidation Disorders Detected by Newborn Screening: Clinical, Biochemical and Genetic Spectrum in a Single‐Center Cohort

open access: yesJIMD Reports, Volume 67, Issue 6, November 2026.
ABSTRACT Newborn screening (NBS) has significantly improved early detection and survival in fatty acid oxidation disorders (FAODs). However, the expanding phenotypic spectrum challenges prognostic stratification, and long‐term morbidity remains incompletely characterized.
Elena Martín‐Hernández   +10 more
wiley   +1 more source

Alcalosis metabólica y tratamiento con Diálisis Peritoneal. A propósito de un caso [PDF]

open access: yes, 2013
La acidosis metabólica que presentan los pacientes en IRC es consecuencia del fallo, por parte de los riñones, de la eliminación de los hidrogeniones.
Julve Ibañéz, Maricel   +3 more
core   +1 more source

Caracterización de los diabéticos tipo 2 con hiperglicemia grave y acidosis metabólica, internados en el Hospital Militar de Luanda, Angola [PDF]

open access: yes, 2023
Introduction: in sub-Saharan Africa, the incidence of metabolic acidosis in diabetics, frequently suffered by those with type 2, is unknown. Objective: to characterize type 2 diabetics with severe hyperglycemia and metabolic acidosis, admitted to the ...
Álvarez Aldana, Dagoberto   +2 more
core  

Associations of severe hyperlactataemia and lactic acidosis in HIV-infected patients receiving antiretroviral theraphy [PDF]

open access: yes, 2007
Includes bibliographical references (leaves 67-70).Severe symptomatic hyperlactataemia and lactic acidosis (SHLA) are life-threatening events that are occurring at increasing incidence levels in South Africa.
Osler, Meg
core   +1 more source

Report of the Scientific Committee of the Spanish Agency for Food Safety and Nutrition (AESAN) on Hereditary Fructose Intolerance (HFI), or aldolase B deficiency, and fructose malabsorption (intestinal fructose intolerance)

open access: yesFood Risk Assess Europe, Volume 4, Issue 2, April 2026.
Abstract Hereditary Fructose Intolerance (HFI), also known as aldolase B deficiency, is an inherited metabolic disorder caused by the deficiency of that enzyme, which participates in the fructose metabolism in the liver, kidneys and small intestine. Aldolase B deficiency brings about the accumulation of fructose‐1‐phosphate in these organs, which can ...
Araceli Díaz Perales   +6 more
wiley   +1 more source

UEG Week 2023 Poster Presentations

open access: yes, 2023
United European Gastroenterology Journal, Volume 11, Issue S8, Page 535-1498, October 2023.
wiley   +1 more source

Experiencia de la acidosis metabólica en pacientes atendidos en la Unidad de Terapia Intensiva del Hospital Infantil de Morelia [PDF]

open access: yes, 2022
Facultad de Ciencias Médicas y Biológicas. Especialidad en PediatríaMetabolic acidosis is an acid-base disorder that occurs frequently during the evolution of critically ill patients, so this work will help us answer several questions about metabolic ...
Alma Jazmín Mosqueda Arreola
core  

Nefrotoxicidad tubular proximal inducida por sobredosis de tenofovir: reporte de un caso de síndrome de Fanconi incompleto

open access: yesRevista Médica Herediana
Mujer de 21 años admitida por intento autolítico tras ingesta de 28 tabletas de tenofovir/lamivudina/dolutegravir, administradas en el contexto de una profilaxis posexposición al virus de la inmunodeficiencia humana (VIH) luego de una agresión sexual ...
Esteban Ochoa-Robles   +4 more
doaj   +1 more source

Valor diagnóstico y pronóstico de la determinación de tripsinógeno-2 urinario en pacientes con pancreatitis aguda

open access: yesAnales del Sistema Sanitario de Navarra, 2010
Fundamento. Estudiar el papel del tripsinógeno-2 urinario en el diagnóstico y pronóstico inicial de pacientes con pancreatitis aguda (PA) así como su relación con la estancia media hospitalaria y la mortalidad. Método.
J.A. Díaz Peromingo   +4 more
doaj   +1 more source

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