Results 101 to 110 of about 4,012 (187)

[How to monitor prediabetes and patients at risk for diabetes. Regarding the validity of diagnostic tests]. [PDF]

Aten Primaria
Maria Tablado MA.
europepmc   +1 more source

Balance of care activity after EMA recommendation for <i>DPYD</i> gene testing in Galicia. [PDF]

Front Pharmacol
Gil-Rodríguez A, Recarey-Rama S, Rodríguez-Viyuela A, Barros F, Carracedo A, Maroñas O.   +5 more
europepmc   +1 more source

Uso de inteligencia artificial en la predisposición genética a enfermedad crítica por COVID-19: evaluación comparativa de modelos de aprendizaje automático. [PDF]

Adv Lab Med
Martin Perez S, Sanchez Jimenez F, Fuentes Cantero S, Jímenez Barragan M, Sanchez Mora C, Borreguero Leon JM, Arrobas Velilla T, Valido Morales A, Delgado Torralbo JA, León-Justel A.   +9 more
europepmc   +1 more source

A hidden enemy: Understanding the hemophagocytic syndrome in children under five years of age in a high-complexity institution in southwestern Colombia [PDF]

Biomedica
Martínez S, Triviño J, Arias O, Medina D, Franco A, Patiño J, Pérez P, Pachajoa H, Rodríguez P, Olaya-Hernández M.   +9 more
europepmc   +1 more source

[Fever after hunting season]. [PDF]

Aten Primaria, 2022
Martínez-Cisneros S, Arbués-Espinosa P, Villagrasa-Boli P.   +2 more
europepmc   +1 more source

[Detection of inborn errors of metabolism: guidelines in Mexico and other countries]. [PDF]

Rev Med Inst Mex Seguro Soc
Guerrero-Barrios S, Chiquillo-Domínguez M, Ayón-Aguilar J, Rodriguez-Alfaro SE, Méndez-Martínez S, García-Flores MA.   +5 more
europepmc   +1 more source

Deficiencia de 3β-hidroxiesteroide deshidrogenasa: una causa rara de hiperplasia adrenal congénita

, 2016
The congenital adrenal hyperplasia corresponds to a group of inherited diseases with enzyme defects that alter the cortisol biosynthesis. The 3β-hydroxysteroid dehydrogenase type 2 deficiency is a rare cause of this defect, where the male genital ...
González Patiño, Angélica, Toro Ramos, Martin, Campuzano Maya, Germán, Monroy, Jennifer, Pineda Trujillo, Nicolás   +4 more
core  

Mecanismo cinético de la L-Alanina Deshidrogenasa de Halobacterium salinarum

, 1999
CICYT (BT87-0033)
openaire   +1 more source

Aldehído Deshidrogenasa Humana en una muestra de la población costarricense

, 2016
This is an electrophoretic study of ALDH isozymes in post-mortem tissue extracts.Three differente electrophoretic variants of the isosyme ALDH3 were found in the 100 individuals examined. One liver sample showed lack of ALDH1. activity, but it remains unknown whether this is due to genetic mechanisms.
Santisteban, Inés, Baudrit Gómez, Félix   +1 more
openaire   +2 more sources

Deficiencia de glucosa-6-fosfato deshidrogenasa: De lo clínico a lo bioquímico

, 2014
"La deficiencia de Glucosa-6-fosfato deshidrogenasa (G6PD) es la enzimopatía más frecuente, con una prevalencia global del 4,9% y con alrededor de 330 a 400 millones de personas afectadas en el mundo. La G6PD desempeña un papel fundamental en el equilibrio redox intracelular, especialmente en los eritrocitos; en condiciones de estrés oxidativo inducido
Saúl Gómez-Manzo, Gabriel López-Velázquez, Itzhel García-Torres, Gloria Hernández-Alcantara, Sara Teresa Méndez-Cruz, Jaime Marcial-Quino, Adriana Castillo-Villanueva, Sergio Enríquez-Flores, Ignacio De la Mora, Angélica Torres-Arroyo, Horacio Reyes-Vivas, Jesús Oria-Hernández   +11 more
openaire   +1 more source