A5045080951- COVID-19 Clinical Research Studies
- Sepsis Diagnosis and Treatment
- Vascular Anomalies and Treatments
- COVID-19 diagnosis using AI
- Sharing Economy and Platforms
- Tracheal and airway disorders
- COVID-19 and healthcare impacts
- Long-Term Effects of COVID-19
- Machine Learning in Healthcare
- Pediatric Pain Management Techniques
- Cancer, Hypoxia, and Metabolism
- SARS-CoV-2 and COVID-19 Research
- Otitis Media and Relapsing Polychondritis
- Metabolism and Genetic Disorders
- RNA Interference and Gene Delivery
- Microscopic Colitis
- CRISPR and Genetic Engineering
- Clostridium difficile and Clostridium perfringens research
- Vascular Malformations and Hemangiomas
- Virus-based gene therapy research
- Renal function and acid-base balance
Hospital Universitario Ramón y Cajal
2020-2025
Universidad de Alcalá
2022-2025
Instituto Ramón y Cajal de Investigación Sanitaria
2020-2025
We aimed to develop and validate a prediction model, based on clinical history examination findings initial diagnosis of coronavirus disease 2019 (COVID-19), identify patients at risk critical outcomes.
Background: Hereditary Hemorrhagic Telangiectasia (HHT) is a vascular autosomically inherited rare disease. Epistaxis (nose bleeds) the most common symptom in HHT, leading to anemia and affecting patient’s quality of life. In addition epistaxis, gastrointestinal bleeding (GI), more often at older ages, may lead severe need for blood transfusions. Thus, finding drugs control both types primary necessity HHT. Methods: A cross-sectional observational study was conducted series 11 HHT patients...
ABSTRACT Objectives Currently available COVID-19 prognostic models have focused on laboratory and radiological data obtained following admission. However, these tests are not initial assessment or in resource-limited settings. We aim to develop validate a prediction model, based clinical history examination findings diagnosis of COVID-19, identify patients at risk critical outcomes. Methods used from the SEMI-COVID-19 Registry, nationwide multicenter cohort consecutive hospitalized for 132...
The availability of highly sensitive molecular tests for the detection Clostridioides difficile in feces leads to overtreatment patients who are probably only colonized. In this prospective study, usefulness fecal calprotectin (fCP) is evaluated a cohort with toxigenic C. feces. Patients were classified by an infectious diseases consultant blinded fCP results into three groups—group I, presumed infection (CDI); group II, doubtful but treated CDI; and III, colonization or self-limited CDI not...
Background: Hereditary Hemorrhagic Telangiectasia (HHT) is a vascular autosomically inherited rare disease. Epistaxis (nose bleeds) the most common symptom in HHT, leading to anemia and affecting patient’s quality of life. In addition epistaxis, gastrointestinal bleeding (GI), more often at older ages, may lead severe need for blood transfussions. Thus, finding drugs control both types primary necessity HHT. Methods: A cross-sectional observational study was conducted series 11 HHT patients...
Lactic acidosis associated with solid neoplasms is a rare complication; its occurrence poorly described, and it poor prognosis. We present the case of an 84-year-old woman who was admitted to internal medicine department diagnosis urinary tract infection accompanied by blood gas analysis showing lactic acidosis. During her admission, abdominal mass evidenced finally diagnosed as undifferentiated carcinoma. wanted emphasize importance correlating clinical laboratory data at time making...