Get started
Author

Angelica Ortiz

Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosis
2004 · Michael A. Dyer, Stacy L. Donovan, et al. · Molecular Brain Research · 52
Loss and recovery of activities of α+ and α isozymes of (Na+ + K+)‐ATPase in cortical focal ischemia: GM1 ganglioside protects plasma membrane structure and function
1992 · S. P. Mahadik, V. A. Bharucha, et al. · Journal of Neuroscience Research · 33
GM1 ganglioside reduces cognitive dysfunction after focal cortical ischemia
1990 · A. Ortiz, J.S. MacDonall, et al. · Pharmacology Biochemistry and Behavior · 22
Estudio del síndrome de Rett en la población española
1999 · Mercè Pineda Marfà, Mª Asunción Aracil Martínez, et al. · Revista de Neurología · 15
Consenso de expertos para el tratamiento de los pacientes con Esclerosis Múltiple en Ecuador.
2024 · Edgar P. Correa-Díaz, Gabriela Acuña, et al. · Revista Ecuatoriana de Neurologia · 1
PDF
Functional correlations of selected AIPL1 mutations found in Leber congenital amaurosis patients and their parents.
2004 · A. Ortiz, Xianhao Wen, et al. · Investigative Ophthalmology & Visual Science · 1
Genetic diagnosis of a case of Rett syndrome
2019 · E. Lepe Balsalobre, R. Rubio Sanchez, et al. · Clinica Chimica Acta
Report of a case of classical congenital suprarrenal hyperplasia
2019 · M.D.M. Viloria Peñas, I. Peral Camacho, et al. · Clinica Chimica Acta
GM1 ganglioside reduces behavioral dysfunction following cortical focal ischemia
1990 · A. Ortiz, James S. MacDonall, et al. · Fordham Research Commons (Fordham University)
Works count: 9
Citation count: 124
H-index: 4
I10-index: 4
Year
Topic
Type