Search Results - "Alonso‐Cotoner, C."
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Randomised clinical trial: the analgesic properties of dietary supplementation with palmitoylethanolamide and polydatin in irritable bowel syndrome
Published in Alimentary Pharmacology & Therapeutics (Suppl) (01-04-2017)“…Summary Background Intestinal immune activation is involved in irritable bowel syndrome (IBS) pathophysiology. While most dietary approaches in IBS involve…”
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The joint power of sex and stress to modulate brain–gut–microbiota axis and intestinal barrier homeostasis: implications for irritable bowel syndrome
Published in Neurogastroenterology and motility (01-04-2016)“…Background Intestinal homeostasis is a dynamic process that takes place at the interface between the lumen and the mucosa of the gastrointestinal tract, where…”
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Cognitive and hedonic responses to meal ingestion correlate with changes in circulating metabolites
Published in Neurogastroenterology and motility (01-12-2016)“…Background We have previously shown that meal ingestion induces cognitive perception (sensations) with a hedonic dimension (well‐being) that depends on the…”
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Current HHT genetic overview in Spain and its phenotypic correlation: data from RiHHTa registry
Published in Orphanet journal of rare diseases (05-06-2020)“…Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is a rare vascular disease with autosomal dominant inheritance. Disease-causing variants in…”
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Genome-wide multi-trait analysis of irritable bowel syndrome and related mental conditions identifies 38 new independent variants
Published in Journal of translational medicine (21-04-2023)“…Irritable bowel syndrome (IBS) is a chronic disorder of gut-brain interaction frequently accompanied by mental conditions, including depression and anxiety…”
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Computerized registry of patients with hemorrhagic hereditary telangiectasia (RiHHTa Registry) in Spain: Objectives, methods, and preliminary results
Published in Revista clínica espanõla (English edition) (01-12-2018)“…INTRODUCTIONHereditary hemorrhagic telangiectasia (HHT) is a rare disease with autosomal dominant inheritance that causes systemic vascular affectation…”
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Computerized registry of patients with hemorrhagic hereditary telangiectasia (RiHHTa Registry) in Spain: Objectives, methods, and preliminary results
Published in Revista clínica espanõla (English edition) (01-12-2018)“…Hereditary hemorrhagic telangiectasia (HHT) is a rare disease with autosomal dominant inheritance that causes systemic vascular affectation. After development…”
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Ferropenia: no siempre son pérdidas
Published in Anales de medicina interna (Madrid, Spain : 1984) (01-05-2003)Get full text
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Iron deficiency: not always blood losses
Published in Anales de medicina interna (Madrid, Spain : 1984) (01-05-2003)“…Iron deficiency may be the only presenting sign of malabsorption due to the presence of intestinal villous atrophy. Once gastrointestinal blood losses have…”
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Ferropenia: no siempre son pérdidas
Published in Anales de medicina interna (Madrid, Spain : 1984) (01-05-2003)“…La ferropenia puede ser la única manifestación de un síndrome malabsortivo, secundario a la presencia de una atrofia intestinal. Por ello, descartadas las…”
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