Results 11 to 20 of about 496 (142)

Publication Only [PDF]

open access: yesHemasphere
HemaSphere, Volume 9, Issue S1, June 2025.
europepmc   +2 more sources

UEG Week 2019 Poster Presentations. [PDF]

open access: yesUnited European Gastroenterol J, 2019
United European Gastroenterology Journal, Volume 7, Issue S8, Page 189-1030, October 2019.
europepmc   +2 more sources

ENFERMEDAD DE MONDOR. PRESENTACIÓN DE UN PACIENTE

open access: yesMedicentro, 2011
La enfermedad de Mondor es una rara entidad de origen desconocido, caracterizada por tromboflebitis de las venas subcutáneas de la pared anterolateral toracoabdominal.
Luis A. Monteagudo de la Guardia   +2 more
doaj   +1 more source

EHA2024 Hybrid Congress [PDF]

open access: yesHemasphere
HemaSphere, Volume 8, Issue S1, June 2024.
europepmc   +2 more sources

[Mondor's disease in a male]. [PDF]

open access: yesAten Primaria, 2004
Matarranz Sanz A, Ramírez Forcada P.
europepmc   +2 more sources

UEG Week 2015 Oral Presentations [PDF]

open access: yesUnited European Gastroenterol J, 2015
United European Gastroenterology Journal, Volume 3, Issue S5, Page 1-145, October 2015.
europepmc   +2 more sources

Enfermedad de Mondor idiopática en seno en un centro de cuidado primario ambulatorio. Reporte de caso [PDF]

open access: yesIatreia
Introducción: la Enfermedad de Mondor (EM) es una tromboflebitis de la pared torácica anterolateral, con solo alrededor de 400 casos reportados a escala mundial, la mayoría en mujeres. Se reporta caso de EM de aparición súbita con dolor, edema y asimetría en seno izquierdo de 2 semanas de evolución.
Daniel Fernando Castro-Goyes   +1 more
openaire   +3 more sources

UEG Week 2015 Poster Presentations [PDF]

open access: yesUnited European Gastroenterol J, 2015
United European Gastroenterology Journal, Volume 3, Issue S5, Page 146-687, October 2015.
europepmc   +2 more sources

Tromboflebitis de presentación inusual

open access: yesGalicia Clínica, 2023
Mondor’s disease is a superficial thrombophlebitis of the thoracic wall. In most cases the aetiology is unknown, although some risk factors have been described. It is a rare, benign condition, with spontaneous resolution occurring in 6 weeks to 6 months,
Tiago C.L.Macedo   +3 more
doaj   +1 more source

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