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1.
An additional patient with SMAD4-Juvenile Polyposis-Hereditary hemorrhagic telangiectasia and connective tissue abnormalities: SMAD4 loss-of-function and gain-of-function pathogenic variants result in contrasting phenotypes.
Am J Med Genet A
; 188(10): 3084-3088, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35869926
2.
Review of the Pathologic Characteristics in Myhre Syndrome: Gain-of-Function Pathogenic Variants in SMAD4 cause a Multisystem Fibroproliferative Response.
Pediatr Dev Pathol
; 25(6): 611-623, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36120950
3.
Early versus delayed treatment with ticagrelor on residual thrombus after percutaneous coronary intervention in patients presenting with non-ST-elevation acute coronary syndrome: an optical coherence tomography study.
Coron Artery Dis
; 31(2): 195-197, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31860559
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