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

Year Number of Results
1977 1
1988 1
1992 1
1996 2
1998 1
2001 3
2005 1
2007 3
2009 1
2010 1
2011 2
2012 2
2013 4
2014 4
2015 1
2016 2
2017 4
2018 1
2024 0

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31 results

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Page 1
The corticospinal tract: Evolution, development, and human disorders.
Welniarz Q, Dusart I, Roze E. Welniarz Q, et al. Dev Neurobiol. 2017 Jul;77(7):810-829. doi: 10.1002/dneu.22455. Epub 2016 Oct 14. Dev Neurobiol. 2017. PMID: 27706924 Review.
The corticospinal tract (CST) plays a major role in cortical control of spinal cord activity. ...These latter disorders result in altered midline crossing at the pyramidal decussation or in the spinal cord, but spare the rest of the CST. ...
The corticospinal tract (CST) plays a major role in cortical control of spinal cord activity. ...These latter disorders result in alt …
Hereditary and metabolic myelopathies.
Hedera P. Hedera P. Handb Clin Neurol. 2016;136:769-85. doi: 10.1016/B978-0-444-53486-6.00038-7. Handb Clin Neurol. 2016. PMID: 27430441 Review.
Hereditary and metabolic myelopathies are a heterogeneous group of neurologic disorders characterized by clinical signs suggesting spinal cord dysfunction. Spastic weakness, limb ataxia without additional cerebellar signs, impaired vibration, and positional sensation are h …
Hereditary and metabolic myelopathies are a heterogeneous group of neurologic disorders characterized by clinical signs suggesting spinal co …
Primary lateral sclerosis.
Singer MA, Statland JM, Wolfe GI, Barohn RJ. Singer MA, et al. Muscle Nerve. 2007 Mar;35(3):291-302. doi: 10.1002/mus.20728. Muscle Nerve. 2007. PMID: 17212349 Review.
The spectrum of motor neuron diseases ranges from disorders that clinically are limited to lower motor neurons to those that exclusively affect upper motor neurons. Primary lateral sclerosis (PLS) is the designation for the syndrome of progressive upper motor neuron dys
The spectrum of motor neuron diseases ranges from disorders that clinically are limited to lower motor neurons to those that exclusively aff …
Transcranial Magnetic Stimulation for the Assessment of Neurodegenerative Disease.
Vucic S, Kiernan MC. Vucic S, et al. Neurotherapeutics. 2017 Jan;14(1):91-106. doi: 10.1007/s13311-016-0487-6. Neurotherapeutics. 2017. PMID: 27830492 Free PMC article. Review.
Abnormalities of TMS outcome measures heralding cortical hyperexcitability, as evidenced by a reduction of short-interval intracortical inhibition and increased in motor-evoked potential amplitude, have been consistently identified as early and intrinsic features of amyotrophic …
Abnormalities of TMS outcome measures heralding cortical hyperexcitability, as evidenced by a reduction of short-interval intracortical inhi …
The recovery of walking in stroke patients: a review.
Jang SH. Jang SH. Int J Rehabil Res. 2010 Dec;33(4):285-9. doi: 10.1097/MRR.0b013e32833f0500. Int J Rehabil Res. 2010. PMID: 20805757 Review.
We reviewed the literature on walking recovery of stroke patients as it relates to the following subjects:epidemiology of walking dysfunction, recovery course of walking, and recovery mechanism of walking (neural control of normal walking, the evaluation methods for leg mo …
We reviewed the literature on walking recovery of stroke patients as it relates to the following subjects:epidemiology of walking dysfunc
Hereditary spastic paraplegia: More than an upper motor neuron disease.
Parodi L, Fenu S, Stevanin G, Durr A. Parodi L, et al. Rev Neurol (Paris). 2017 May;173(5):352-360. doi: 10.1016/j.neurol.2017.03.034. Epub 2017 Apr 24. Rev Neurol (Paris). 2017. PMID: 28449883 Review.
Based on symptoms, HSPs can be divided into pure forms, presenting with pyramidal signs leading to lower-limb spasticity, and complex forms, when additional neurological or extraneurological symptoms are detected. ...The pathogenic mutations of SPGs primarily lead to progr …
Based on symptoms, HSPs can be divided into pure forms, presenting with pyramidal signs leading to lower-limb spasticity, and complex …
Neurophysiological mechanisms and functional impact of mirror movements in children with unilateral spastic cerebral palsy.
Kuo HC, Friel KM, Gordon AM. Kuo HC, et al. Dev Med Child Neurol. 2018 Feb;60(2):155-161. doi: 10.1111/dmcn.13524. Epub 2017 Sep 8. Dev Med Child Neurol. 2018. PMID: 28884806 Free PMC article. Review.
We suggest two premises: (1) the presence of mirror movements is indicative of an ipsilateral corticospinal tract reorganization; and (2) the corticospinal tract organization may affect patients' responses to certain treatment. ...WHAT THIS PAPER ADDS: Mirror moveme …
We suggest two premises: (1) the presence of mirror movements is indicative of an ipsilateral corticospinal tract reorganization; and …
Neuroimaging in amyotrophic lateral sclerosis: insights into structural and functional changes.
Chiò A, Pagani M, Agosta F, Calvo A, Cistaro A, Filippi M. Chiò A, et al. Lancet Neurol. 2014 Dec;13(12):1228-40. doi: 10.1016/S1474-4422(14)70167-X. Epub 2014 Nov 10. Lancet Neurol. 2014. PMID: 25453462 Review.
In the past two decades, structural and functional neuroimaging findings have greatly modified longstanding notions regarding the pathophysiology of amyotrophic lateral sclerosis (ALS). Neuroimaging studies have shown that anatomical and functional lesions sp …
In the past two decades, structural and functional neuroimaging findings have greatly modified longstanding notions regarding the pat …
Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights.
Vucic S, Ziemann U, Eisen A, Hallett M, Kiernan MC. Vucic S, et al. J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1161-70. doi: 10.1136/jnnp-2012-304019. Epub 2012 Dec 21. J Neurol Neurosurg Psychiatry. 2013. PMID: 23264687 Free PMC article. Review.
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder of the motor neurons in the motor cortex, brainstem and spinal cord. ...To date, TMS studies have established motor cortical and corticospinal dysfunction in ALS, with cor …
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder of the motor neurons in the motor cortex, bra …
Zebrafish models of human motor neuron diseases: advantages and limitations.
Babin PJ, Goizet C, Raldúa D. Babin PJ, et al. Prog Neurobiol. 2014 Jul;118:36-58. doi: 10.1016/j.pneurobio.2014.03.001. Epub 2014 Apr 3. Prog Neurobiol. 2014. PMID: 24705136 Free article. Review.
In contrast, spinal muscular atrophy (SMA) involves the specific degeneration of LMNs, with symmetrical muscle weakness and atrophy. Amyotrophic lateral sclerosis (ALS), the most common adult-onset MND, is characterized by the degeneration of both UMNs and LMNs, leading to …
In contrast, spinal muscular atrophy (SMA) involves the specific degeneration of LMNs, with symmetrical muscle weakness and atrophy. Amyotro …
31 results