Results 121 to 130 of about 46,051 (178)

De novo emergence of the mutation E484K in a SARS-CoV-2 B.1.1.7 lineage variant. [PDF]

open access: yesEnferm Infecc Microbiol Clin (Engl Ed), 2021
Urrutikoetxea-Gutierrez M   +3 more
europepmc   +1 more source

[SARS-CoV-2 variants, a still unfinished story]. [PDF]

open access: yesVacunas, 2021
Pérez-Abeledo M, Sanz Moreno JC.
europepmc   +1 more source

Compound Heterozygous Familial Hypercholesterolemia Caused by LDLR Variants. [PDF]

open access: yesArq Bras Cardiol, 2020
Pamplona-Cunha H   +4 more
europepmc   +1 more source

[Septic shock and empyema induced by Pasteurella multocida]. [PDF]

open access: yesRev Esp Quimioter, 2021
Fernández Vecilla D   +3 more
europepmc   +1 more source

Natural SARS-CoV- 2 infection in domestic cats and dogs of humans diagnosed with COVID-19 in Valle de Aburrá, Antioquia [PDF]

open access: yesBiomedica, 2022
Cabrera A   +5 more
europepmc   +1 more source

Fenilcetonuria e hiperfenilalaninemia en recién nacidos

open access: yesSalud Uninorte, 2003
La fenilcetonuria pertenece al grupo de las hiperfenilalaninemias. Es una enfermedad infantil, metabólica, causada por un déficit de la enzima (sustancia proteica capaz de activar indirectamente una reacción química definida) del hígado llamada ...
Mayra Escaf
doaj  

[X-linked intellectual disability syndrome with macrocephaly due to BRWD3 gene deletion]. [PDF]

open access: yesRev Neurol
Arroyo-Carrera I   +4 more
europepmc   +1 more source

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