Evolución de paciente pediátrico con Síndrome Alagille. Reporte de caso
El síndrome de Alagille es una enfermedad congénita y poco frecuente, se transmite de forma autosómica dominante, con expresividad variable. Se caracteriza por presentar colestasis, anomalías vertebrales y oculares, cardiopatía congénita y dismorfias ...
Estela V Román Castellini +3 more
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[Cutaneous manifestations in the current pandemic of coronavirus infection disease (COVID 2019)]. [PDF]
Morey-Olivé M +4 more
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[Hepatitis associated aplastic anemia during SARS-CoV-2 pandemic]. [PDF]
Santarelli IM +7 more
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[DRESS Syndrome in a Patient With SARS-CoV-2 Disease]. [PDF]
Riveiro V +3 more
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[Generalized Amyloid Lichen Associated with Primary Biliary Cholangitis: A Case Report]. [PDF]
Pardo Escalera EJ +2 more
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[Multisystem inflammatory syndrome in a young infant with lymphocytosis and reactive thrombocytosis post COVID-19: Case report]. [PDF]
Vera-Rodríguez HA +5 more
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[Simple gastroschisis complicated by multiple perforations, frozen abdomen, and loss of abdominal domain]. [PDF]
Cayetano Cabrera D +5 more
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Signos de alarma al regresar de un viaje. [PDF]
Valerio L, Martín-Cano SRYL.
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[A descriptive overview of cases of congenital cytomegalovirus at a tertiary hospital between 2017 and 2023]. [PDF]
Medina García E +7 more
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