Results 41 to 50 of about 62,890 (168)
Abstract Book for the 27th Congress of the European Hematology Association
, 2022 HemaSphere, Volume 6, Issue S3, Page 1-4130, June 2022.
wiley +1 more source
Acidosis tubular renal asociado a Síndrome de Sjögren primario
Revista Clínica de la Escuela de Medicina UCR-HSJD, 2019 Paciente femenina de 14 años, previamente sana, que se presentó con hallazgos clínicos de paraparesia asociado a artralgias. En los laboratorios presentó hipokalemia, acidosis metabólica con brecha aniónica normal y proteinuria. Se hizo el diagnóstico de
David Méndez Ramírez +1 more
doaj +1 more source
JIMD Reports, Volume 66, Issue 3, May 2025.ABSTRACT The current standard diet for long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) in the first months of life includes a special formula low in long‐chain triglycerides (LCT) and enriched in medium‐chain triglycerides (MCT). It involves the interruption of breastfeeding, withholding its nutritional and nonnutritional benefits.
Clara Alonso‐Diaz +7 more
wiley +1 more source
Triggering of erythropoietin production by hypoxia is inhibited by respiratory and metabolic acidosis [PDF]
, 1990 Erythropoietin (EPO) production in response to hypoxic hypoxia is known to be attenuated by simultaneous hypercapnia. This study aimed to investigate whether this inhibitory effect of hypercapnia is 1) a direct effect of carbon dioxide or mediated by ...
Eckardt, K. U. +9 more
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Severe hyperchloremic metabolic acidosis with SGLT2 inhibitors in patients with urinary diversion
Nefrología (English Edition)Urinary diversion after cystectomy using autologous intestinal segments has been the gold standard treatment in several urinary tract diseases. The most frequent metabolic consequence is hyperchloremic metabolic acidosis, due to ammonium hydrogen and ...
Carolina Gomes +5 more
doaj +3 more sources
New variants expand the neurological phenotype of COQ7 deficiency
Journal of Inherited Metabolic Disease, Volume 47, Issue 5, Page 1047-1068, September 2024.Abstract The protein encoded by COQ7 is required for CoQ10 synthesis in humans, hydroxylating 3‐demethoxyubiquinol (DMQ10) in the second to last steps of the pathway. COQ7 mutations lead to a primary CoQ10 deficiency syndrome associated with a pleiotropic neurological disorder.
María Alcázar Fabra +33 more
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, 2009 Este trabajo recopila información concerniente a la acidosis metabólica en equinos causada por un fallo renal crónico, su etiología, fisiopatología, mecanismos compensatorios renales, pulmonares y hepáticos y hace una comparación de los diversos ...
Gómez, Daniel
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Predicción de mortalidad en pacientes con dengue grave en Unidad de Cuidados Intensivos
Revista Información Científica, 2018 Introducción: el dengue constituye un importante problema de salud pública para las regiones endémicas. Objetivo: identificar variables clínicas, biológicas e imaginológicas asociadas a la probabilidad de morir en pacientes con dengue grave ingresados en
Yunieski Griñán Garrido +2 more
doaj
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias
Journal of Inherited Metabolic Disease, Volume 47, Issue 4, Page 674-689, July 2024.Abstract The current German newborn screening (NBS) panel includes 13 inherited metabolic diseases (IMDs). In addition, a NBS pilot study in Southwest Germany identifies individuals with propionic acidemia (PA), methylmalonic acidemia (MMA), combined and isolated remethylation disorders (e.g., cobalamin [cbl] C and methylenetetrahydrofolate reductase ...
Anna T. Reischl‐Hajiabadi +20 more
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Revista de la Facultad de Medicina HumanaIntroducción: La sepsis neonatal de inicio tardío (SNT) es una infección nosocomial frecuente y letal en neonatos prematuros hospitalizados. Objetivos: Identificar factores de riesgo para mortalidad en SNT confirmada por hemocultivo en el Instituto ...
Carmen Davila Aliaga +6 more
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