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1998 3
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Page 1
Sporadic adult-onset ataxia.
Klockgether T. Klockgether T. Handb Clin Neurol. 2018;155:217-225. doi: 10.1016/B978-0-444-64189-2.00014-7. Handb Clin Neurol. 2018. PMID: 29891060 Review.
It is distinguished from hereditary ataxias and from acquired ataxias. SAOA also needs to be differentiated from multiple system atrophy of cerebellar type (MSA-C). Thus, the diagnosis of SAOA can only be made by exclusion. Although cerebellar ataxia is the prominent sympt …
It is distinguished from hereditary ataxias and from acquired ataxias. SAOA also needs to be differentiated from multiple system atrophy …
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.
This review of the neuropathology of Friedreich ataxia stresses the critical role of hypoplasia and superimposed atrophy of dorsal root ganglia. Progressive destruction of dorsal root ganglia accounts for thinning of dorsal roots, degeneration of dorsal columns, transsynap …
This review of the neuropathology of Friedreich ataxia stresses the critical role of hypoplasia and superimposed atrophy of dorsal ro …
Breathing and the nervous system.
Urfy MZ, Suarez JI. Urfy MZ, et al. Handb Clin Neurol. 2014;119:241-50. doi: 10.1016/B978-0-7020-4086-3.00017-5. Handb Clin Neurol. 2014. PMID: 24365300 Review.
It involves cortical (volitional) as well as subcortical (automatic) output. Cortical output is mainly through the corticospinal tract, whereas the brainstem sends signals via the reticulospinal tract. ...Various neurologic disorders such as stroke or neurode …
It involves cortical (volitional) as well as subcortical (automatic) output. Cortical output is mainly through the corticospinal t …
Central motor conduction time.
Udupa K, Chen R. Udupa K, et al. Handb Clin Neurol. 2013;116:375-86. doi: 10.1016/B978-0-444-53497-2.00031-0. Handb Clin Neurol. 2013. PMID: 24112910 Review.
Prolongation of CMCT occurs due to slowing of conduction through rapidly conducting corticospinal fibers, as seen in various disorders such as demyelinating diseases (multiple sclerosis, MS), amyotrophic lateral sclerosis, structural lesions in the corticospinal …
Prolongation of CMCT occurs due to slowing of conduction through rapidly conducting corticospinal fibers, as seen in various disorder …
Childhood-Onset Hereditary Spastic Paraplegia (HSP): A Case Series and Review of Literature.
Panwala TF, Garcia-Santibanez R, Vizcarra JA, Garcia AG, Verma S. Panwala TF, et al. Pediatr Neurol. 2022 May;130:7-13. doi: 10.1016/j.pediatrneurol.2022.02.007. Epub 2022 Mar 3. Pediatr Neurol. 2022. PMID: 35303589 Review.
BACKGROUND: Hereditary spastic paraplegia (HSP) encompasses several rare genetic disorders characterized by progressive lower extremity spasticity and weakness caused by corticospinal tract degeneration. Published literature on genetically confirmed pediatric HSP ca …
BACKGROUND: Hereditary spastic paraplegia (HSP) encompasses several rare genetic disorders characterized by progressive lower extremity spas …
Spinocerebellar ataxia type 7.
Martin JJ. Martin JJ. Handb Clin Neurol. 2012;103:475-91. doi: 10.1016/B978-0-444-51892-7.00030-9. Handb Clin Neurol. 2012. PMID: 21827908 Review.
The diagnosis is made by molecular genetics. The neuropathology of the disorder includes atrophy of the spinocerebellar pathways, pyramidal tracts, and motor nuclei in the brainstem and spinal cord, a cone-rod sytrophy of the retina, and ataxin-7 immunoreacti …
The diagnosis is made by molecular genetics. The neuropathology of the disorder includes atrophy of the spinocerebellar pathways, …
Hereditary dentatorubral-pallidoluysian atrophy.
Oyanagi S. Oyanagi S. Neuropathology. 2000 Sep;20 Suppl:S42-6. doi: 10.1046/j.1440-1789.2000.00307.x. Neuropathology. 2000. PMID: 11037186 Review.
Pathology and associated clinical symptoms of hereditary dentatorubral-pallidoluysian atrophy (H-DRPLA) which was established as a new inherited neurodegenerative disease in 1982 are described. Obligatory lesions in the central nervous system combine with degeneration of t …
Pathology and associated clinical symptoms of hereditary dentatorubral-pallidoluysian atrophy (H-DRPLA) which was established as a ne …
[Fukuhara disease].
Fukuhara N. Fukuhara N. Brain Nerve. 2008 Jan;60(1):53-8. Brain Nerve. 2008. PMID: 18232333 Review. Japanese.
Patients with MERRF develop myoclonus, epileptic seizures, cerebellar ataxia, dementia, sensorineural hearing disturbance, optic atrophy, muscular wasting, and foot deformities at the advanced stage. Pathological findings show degeneration of the dentate nuclei, globus pal …
Patients with MERRF develop myoclonus, epileptic seizures, cerebellar ataxia, dementia, sensorineural hearing disturbance, optic atrophy …
Neuromuscular contributions to age-related weakness.
Clark DJ, Fielding RA. Clark DJ, et al. J Gerontol A Biol Sci Med Sci. 2012 Jan;67(1):41-7. doi: 10.1093/gerona/glr041. Epub 2011 Mar 17. J Gerontol A Biol Sci Med Sci. 2012. PMID: 21415261 Free PMC article. Review.
Diffusion Magnetic Resonance Imaging Microstructural Abnormalities in Multiple System Atrophy: A Comprehensive Review.
Pasquini J, Firbank MJ, Ceravolo R, Silani V, Pavese N. Pasquini J, et al. Mov Disord. 2022 Oct;37(10):1963-1984. doi: 10.1002/mds.29195. Epub 2022 Aug 29. Mov Disord. 2022. PMID: 36036378 Free PMC article. Review.
Multiple system atrophy (MSA) is a neurodegenerative disease characterized by autonomic failure, ataxia, and/or parkinsonism. ...Widespread microstructural abnormalities of white matter were described, especially in the middle cerebellar peduncle, corticospinal t …
Multiple system atrophy (MSA) is a neurodegenerative disease characterized by autonomic failure, ataxia, and/or parkinsonism. ...Wide …
45 results