Results 81 to 90 of about 680 (108)
Evaluación tras 12 meses de las características de una población con diabetes tipo 2 del Área Sur de Tenerife sometidas a tratamiento farmacológico combinado [PDF]
, 2018 Marrero García, Melody
core
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Valores de referencia de la actividad enzimática alfa-glucosidasa ácida linfocitaria
Revista del Laboratorio Clínico, 2016Resumen Introduccion La enfermedad de Pompe, tambien denominada deficit de maltasa acida o glucogenosis tipo ii, es un trastorno metabolico autosomico recesivo caracterizado por un acumulo anormal de glucogeno lisosomal, causado por la deficiencia de la enzima α-glucosidasa acida (GAA). Segun la edad de inicio y el grado de afectacion organica, la
Borja del Castillo Figueruelo +3 more
openaire +1 more source
Revista de Neurología, 2013
INTRODUCTION. Glycogen storage disease type II, or Pompe disease, is a lysosomal disease with an autosomal recessive pattern of inheritance. Late-onset Pompe disease is a progressive metabolic myopathy caused by decreased activity of the enzyme acid alpha-glucosidase (GAA), which gives rise to reduced degradation and later accumulation of glycogen in ...
José Guevara Campos +3 more
openaire +1 more source
INTRODUCTION. Glycogen storage disease type II, or Pompe disease, is a lysosomal disease with an autosomal recessive pattern of inheritance. Late-onset Pompe disease is a progressive metabolic myopathy caused by decreased activity of the enzyme acid alpha-glucosidase (GAA), which gives rise to reduced degradation and later accumulation of glycogen in ...
José Guevara Campos +3 more
openaire +1 more source
Estigmas de maices autóctonos Mexicanos y su capacidad para inhibir alfa-glucosidasas intestinales.
2017Alvarado-Díaz, Samara +1 more
openaire +1 more source
Efanesoctocog Alfa Prophylaxis for Patients with Severe Hemophilia A
New England Journal of Medicine, 2023Angela C Weyand
exaly