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Mostrando ítems 41-50 de 92
Nonneurological Involvement In Late-onset Friedreich Ataxia (lofa): Exploring The Phenotypes
(Springer New York LLC, 2016)
Exploring iron-binding to human frataxin and to selected Friedreich ataxia mutants by means of NMR and EPR spectroscopies
(Elsevier Science, 2019-11)
The neurodegenerative disease Friedreich ataxia results from a deficiency of frataxin, a mitochondrial protein. Most patients have a GAA expansion in the first intron of both alleles of frataxin gene, whereas a minority ...
Protocolo de ejercicios beneficos para el mejoramiento de las actividades basicas cotidianas (abc) a traves de la fuerza muscular, en personas con sindrome de ataxia de friedreich
(Unidad Central del Valle del CaucaLicenciatura en Educación Física, Recreación y DeporteFacultad de Ciencias de la EducaciónTuluá, Valle del Cauca, Colombia, 2008)
El estudio de caso surgió gracias a la práctica profesional docente, elegida en el
área de salud, con personas en situación de discapacidad, mientras se cursaba el
decimo segundo (XII) semestre, en la Facultad de Ciencias ...
Yeast frataxin mutants display decreased superoxide dismutase activity crucial to promote protein oxidative damage
(Elsevier Science Inc, 2010-02-01)
Iron overload is involved in several pathological conditions, including Friedreich ataxia, a disease caused by decreased expression of the mitochondrial protein frataxin. In a previous study, we identified 14 proteins ...
Frataxin deficiency in neonatal rat ventricular myocytes targets mitochondria and lipid metabolism
(Elsevier, 2014-08)
Friedreich ataxia (FRDA) is a hereditary disease caused by deficient frataxin expression. This mitochondrial protein has been related to iron homeostasis, energy metabolism, and oxidative stress. Patients with FRDA experience ...
Mri Texture Analysis Reveals Bulbar Abnormalities In Friedreich Ataxia
(AMER SOC NEURORADIOLOGYDENVILLE, 2015)
Olfactory impairment in familial ataxias
(Bmj Publishing GroupLondon, 2012)