Hipercoagulabilidad en el Síndrome de Prader Willi
La síndrome de Prader-Willi (SPW) és un trastorn genètic complex causat per una alteració en l'impronta del cromosoma 15q11–q13. Es caracteritza clínicament per hipotonia neonatal, hiperfàgia, obesitat severa, disfunció endocrina i alteracions cognitives i conductuals. Entre les seves múltiples complicacions, destaca l’increment del risc cardiovascular,
openaire +1 more source
TROMBOEMBOLISMO: EFEITO DA HIPERCOAGULABILIDADE DA SÍNDROME HELLP NO PÓS-PARTO?
M.R. Castro +6 more
openaire +2 more sources
[Ischemic Priapism: evaluation in a third-level hospital in Mexico]. [PDF]
Sánchez-Villaseñor G +6 more
europepmc +1 more source
[SARS-CoV-2 infection and ischemic stroke]. [PDF]
Marín-Medina DS +3 more
europepmc +1 more source
[Comments on the article "Changes in hypertensive control 2020-2021 in a family medicine unit"]. [PDF]
Ahumada-Pérez J.
europepmc +1 more source
[Knowledge of thromboprophylaxis-COVID-19 in healthcare professionals in Spain]. [PDF]
García Vallejo O +6 more
europepmc +1 more source
[Atypical clinical and mortality in older adults hospitalized with COVID-19 pneumonia]. [PDF]
Valencia-Blancas T +4 more
europepmc +1 more source
[Assessment of pulmonary embolism related to active SARS-CoV-2 infection in pregnant women.] [PDF]
Moreno-Ballesteros A +5 more
europepmc +1 more source
[Clinical, diagnostic and therapeutic profile of patients with left intraventricular thrombus in three high-complexity centers during the period 2000-2022]. [PDF]
Lozano Pineda F +9 more
europepmc +1 more source

