Results 91 to 100 of about 312 (147)

Hipercoagulabilidad en el Síndrome de Prader Willi

open access: yes
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?

open access: yesHematology, Transfusion and Cell Therapy, 2020
M.R. Castro   +6 more
openaire   +2 more sources

[Ischemic Priapism: evaluation in a third-level hospital in Mexico]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Sánchez-Villaseñor G   +6 more
europepmc   +1 more source

[SARS-CoV-2 infection and ischemic stroke]. [PDF]

open access: yesSemergen, 2021
Marín-Medina DS   +3 more
europepmc   +1 more source

[Knowledge of thromboprophylaxis-COVID-19 in healthcare professionals in Spain]. [PDF]

open access: yesSemergen, 2021
García Vallejo O   +6 more
europepmc   +1 more source

[Atypical clinical and mortality in older adults hospitalized with COVID-19 pneumonia]. [PDF]

open access: yesRev Med Inst Mex Seguro Soc
Valencia-Blancas T   +4 more
europepmc   +1 more source

[Assessment of pulmonary embolism related to active SARS-CoV-2 infection in pregnant women.] [PDF]

open access: yesRev Esp Med Nucl Imagen Mol, 2022
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]

open access: yesArch Peru Cardiol Cir Cardiovasc
Lozano Pineda F   +9 more
europepmc   +1 more source

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