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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1957 1
1967 2
1968 2
1972 1
1974 1
1979 3
1982 2
1983 1
1984 1
1990 2
1991 1
1993 2
1995 2
1997 2
1998 1
2001 1
2004 1
2006 2
2007 2
2009 4
2010 2
2011 3
2012 4
2013 7
2014 4
2015 4
2016 4
2017 10
2018 4
2019 2
2020 5
2021 5
2023 3
2024 0

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84 results

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Page 1
Oxidative stress and mitochondrial dysfunction-linked neurodegenerative disorders.
Islam MT. Islam MT. Neurol Res. 2017 Jan;39(1):73-82. doi: 10.1080/01616412.2016.1251711. Epub 2016 Nov 3. Neurol Res. 2017. PMID: 27809706 Review.
Oxidative stress has been considered to be linked to the etiology of many diseases, including neurodegenerative diseases (NDDs) such as Alzheimer diseases, Amyotrophic lateral sclerosis, Friedreich's ataxia, Huntington's disease, Multiple sclerosis, and Parkinson's …
Oxidative stress has been considered to be linked to the etiology of many diseases, including neurodegenerative diseases (NDDs) such as Alzh …
Friedreich Ataxia: Hypoplasia of Spinal Cord and Dorsal Root Ganglia.
Koeppen AH, Becker AB, Qian J, Feustel PJ. Koeppen AH, et al. J Neuropathol Exp Neurol. 2017 Feb 1;76(2):101-108. doi: 10.1093/jnen/nlw111. J Neuropathol Exp Neurol. 2017. PMID: 28082326
After Friedreich's description in 1877, depletion of myelinated fibers in the dorsal columns, dorsal spinocerebellar and lateral corticospinal tracts, and neuronal loss in the dorsal nuclei of Clarke columns were considered unique and essential neuropathological features o …
After Friedreich's description in 1877, depletion of myelinated fibers in the dorsal columns, dorsal spinocerebellar and lateral cort …
Friedreich ataxia: neuropathology revised.
Koeppen AH, Mazurkiewicz JE. Koeppen AH, et al. J Neuropathol Exp Neurol. 2013 Feb;72(2):78-90. doi: 10.1097/NEN.0b013e31827e5762. J Neuropathol Exp Neurol. 2013. PMID: 23334592 Free PMC article. Review.
Friedreich ataxia is an autosomal recessive disorder that affects children and young adults. ...In light of the selective vulnerability of organs and tissues to systemic frataxin deficiency, many questions about the pathogenesis of Friedreich ataxia re …
Friedreich ataxia is an autosomal recessive disorder that affects children and young adults. ...In light of the selective vuln …
Milestones in Friedreich ataxia: more than a century and still learning.
Abrahão A, Pedroso JL, Braga-Neto P, Bor-Seng-Shu E, de Carvalho Aguiar P, Barsottini OG. Abrahão A, et al. Neurogenetics. 2015 Jul;16(3):151-60. doi: 10.1007/s10048-015-0439-z. Epub 2015 Feb 8. Neurogenetics. 2015. PMID: 25662948 Review.
Friedreich ataxia (FRDA) is the most common autosomal recessive ataxia worldwide. ...The molecular and metabolic disturbances, including iron accumulation, lead to pathological changes characterized by spinal cord and dorsal root ganglia atrophy …
Friedreich ataxia (FRDA) is the most common autosomal recessive ataxia worldwide. ...The molecular and metabolic distur …
Mitochondrial pathophysiology in Friedreich's ataxia.
González-Cabo P, Palau F. González-Cabo P, et al. J Neurochem. 2013 Aug;126 Suppl 1:53-64. doi: 10.1111/jnc.12303. J Neurochem. 2013. PMID: 23859341 Free article. Review.
Neurological examination indicates that Friedreich's ataxia corresponds to a mixed sensory and cerebellar ataxia, which affects the proprioceptive pathways. Neuropathology and pathophysiology of Friedreich's ataxia involves the peripheral sensor …
Neurological examination indicates that Friedreich's ataxia corresponds to a mixed sensory and cerebellar ataxia, which …
Mitochondrial impairment, decreased sirtuin activity and protein acetylation in dorsal root ganglia in Friedreich Ataxia models.
Sanz-Alcázar A, Britti E, Delaspre F, Medina-Carbonero M, Pazos-Gil M, Tamarit J, Ros J, Cabiscol E. Sanz-Alcázar A, et al. Cell Mol Life Sci. 2023 Dec 21;81(1):12. doi: 10.1007/s00018-023-05064-4. Cell Mol Life Sci. 2023. PMID: 38129330 Free PMC article.
Friedreich ataxia (FA) is a rare, recessive neuro-cardiodegenerative disease caused by deficiency of the mitochondrial protein frataxin. ...
Friedreich ataxia (FA) is a rare, recessive neuro-cardiodegenerative disease caused by deficiency of the mitochondrial protein …
Friedreich ataxia: the clinical picture.
Pandolfo M. Pandolfo M. J Neurol. 2009 Mar;256 Suppl 1:3-8. doi: 10.1007/s00415-009-1002-3. J Neurol. 2009. PMID: 19283344 Review.
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder that affects approximately 1 in 50,000 Caucasians. ...Approximately 10 % of patients with FRDA develop diabetes. The neuronopathy in the dorsal root ganglia, accompanied by the loss of …
Friedreich ataxia (FRDA) is a rare autosomal recessive hereditary disorder that affects approximately 1 in 50,000 Caucasians. …
Dorsal root ganglia in Friedreich ataxia: satellite cell proliferation and inflammation.
Koeppen AH, Ramirez RL, Becker AB, Mazurkiewicz JE. Koeppen AH, et al. Acta Neuropathol Commun. 2016 May 3;4(1):46. doi: 10.1186/s40478-016-0288-5. Acta Neuropathol Commun. 2016. PMID: 27142428 Free PMC article.
INTRODUCTION: Dorsal root ganglia (DRG) are highly vulnerable to frataxin deficiency in Friedreich ataxia (FA), an autosomal recessive disease due to pathogenic homozygous guanine-adenine-adenine trinucleotide repeat expansions in intron 1 of the FXN gene (ch …
INTRODUCTION: Dorsal root ganglia (DRG) are highly vulnerable to frataxin deficiency in Friedreich ataxia (FA), an auto …
Apparent Opportunities and Hidden Pitfalls: The Conflicting Results of Restoring NRF2-Regulated Redox Metabolism in Friedreich's Ataxia Pre-Clinical Models and Clinical Trials.
Tiberi J, Segatto M, Fiorenza MT, La Rosa P. Tiberi J, et al. Biomedicines. 2023 Apr 27;11(5):1293. doi: 10.3390/biomedicines11051293. Biomedicines. 2023. PMID: 37238963 Free PMC article. Review.
Friedreich's ataxia (FRDA) is an autosomal, recessive, inherited neurodegenerative disease caused by the loss of activity of the mitochondrial protein frataxin (FXN), which primarily affects dorsal root ganglia, cerebellum, and spinal cord neurons. ...
Friedreich's ataxia (FRDA) is an autosomal, recessive, inherited neurodegenerative disease caused by the loss of activity of t …
Neuroimaging Applications in Chronic Ataxias.
Mascalchi M, Vella A. Mascalchi M, et al. Int Rev Neurobiol. 2018;143:109-162. doi: 10.1016/bs.irn.2018.09.011. Epub 2018 Oct 29. Int Rev Neurobiol. 2018. PMID: 30473193 Review.
In fact spinal atrophy is observed in Friedreich ataxia, cortical cerebellar atrophy in Ataxia Telangectasia, gluten ataxia and Sporadic Adult Onset Ataxia and olivopontocerebellar atrophy in Multiple System Atrophy cerebellar type. ...Th …
In fact spinal atrophy is observed in Friedreich ataxia, cortical cerebellar atrophy in Ataxia Telangectasia, gl …
84 results