Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Luis Jiménez Jiménez"'
Autor:
Anurag Kashyap, Álvaro Luis Jiménez‐Jiménez, Weiqi Zhang, Montserrat Capellades, Sumithra Srinivasan, Anna Laromaine, Olga Serra, Mercè Figueras, Jorge Rencoret, Ana Gutiérrez, Marc Valls, Nuria S. Coll
Publikováno v:
New Phytologist. 235:2496-2496
Autor:
Myriam, Ley-Martos, María J, Salado-Reyes, Raúl, Espinosa-Rosso, Jesús, Solera-García, Luis, Jiménez-Jiménez
Publikováno v:
Revista de neurologia. 61(9)
Pompe disease is a generalized progressive disease caused by a deficiency of the lysosome enzyme acid alpha-glucosidase (GAA). We present three cases with different clinical symptomatology and treated with enzyme replacement therapy (ERT) with positi
Autor:
Luis Jiménez Jiménez, Encarnación Pamies-Andréu, Ovidio Muñiz Grijalvo, Pablo Stiefel García Junco, Verónica Alfaro Lara, Salvador García Morillo, José Villar Ortiz, Antonio J Vallejo-Vaz, María Luisa Miranda Guisado
Publikováno v:
Hypertension research : official journal of the Japanese Society of Hypertension. 35(3)
Increased levels of oxidative stress have been demonstrated in Preeclampsia in previous studies, but this finding has not been established in other hypertensive disorders in pregnancy (HDP). We measured different markers of lipid peroxidation and ant
Autor:
Carlos, Macías Blanco, Daniel, Fatela-Cantillo, Luis, Jiménez-Jiménez, Raúl, López Aguilar, Rafael, Moreno-Luna, Antonio, Doblas Delgado, Pablo, Stiefel
Publikováno v:
Medicina clinica. 138(4)
To evaluate the association between circulating biomarkers of collagen metabolism in serum, left ventricular mass index (LVMI) and diastolic dysfunction in patients with resistant hypertension.Fifty-two patients with resistant hypertension and 24 hea
Autor:
Jesús Solera-García, Raúl Espinosa-Rosso, Luis Jiménez-Jiménez, María J Salado-Reyes, Myriam Ley-Martos
Publikováno v:
Revista de Neurología. 61:416
Introduccion. La enfermedad de Pompe es un trastorno generalizado progresivo producido por el deficit de la enzima alfa-glucosidasa acida (AGA) de los lisosomas. Se presentan tres casos manifestados de forma muy diferente y tratados con terapia enzim