Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Maylín Pupo Infante"'
Autor:
Anett Rubio Torres, Greilys Morejón García, Liliana Hernández Pérez, Yesdiley Lafita Delfino, Maylín Pupo Infante, Sadys Feal Carballo, Elisa M. Castells Martínez, Alik Rosabal Poloshkov, Ernesto Carlos González Reyes, Milenén Hernández Marín, Pedro L. Pérez Mora, Joel M. Quintana Guerra, Iria García de la Rosa
Publikováno v:
Clinica Chimica Acta. 485:311-315
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by the deficiency of one of the five enzymes involved in the biosynthesis of corticosteroids. The most common form of the disease is the lack of 21-hydroxylase which provo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33ff063b99a17454819aafb3c331250
https://doi.org/10.1016/j.cca.2018.07.019
https://doi.org/10.1016/j.cca.2018.07.019
Autor:
Pedro Lucio Pérez Morás, Pedro Rolando Almenares Guasch, Luisa Martínez Beltrán, Iria García de la Rosa, Elisa María Castells Martínez, Greilys Morejón García, Amarilys Frómeta Suárez, Joel M. Quintana Guerra, Mary Triny Segura González, Sadys Feal Carballo, Maylín Pupo Infante, Liliana Hernández Pérez, Yesdiley Lafita Delfino
Publikováno v:
Journal of immunoassayimmunochemistry. 40(4)
Congenital hypothyroidism (CH) is one of the most frequent inherited-metabolic diseases in the world, and the main cause of treatable mental retardation in children. Because signs and symptoms of this disease are often scarce and not easily recogniza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::976c811a3464fa0dd8fcf7fb92ffbfe8
https://pubmed.ncbi.nlm.nih.gov/31043143
https://pubmed.ncbi.nlm.nih.gov/31043143