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

Year Number of Results
1979 1
1983 3
1985 2
1987 6
1988 7
1989 5
1990 5
1991 15
1992 11
1993 14
1994 13
1995 10
1996 18
1997 16
1998 10
1999 17
2000 13
2001 25
2002 21
2003 31
2004 21
2005 22
2006 21
2007 25
2008 23
2009 26
2010 21
2011 25
2012 30
2013 39
2014 34
2015 29
2016 30
2017 25
2018 31
2019 32
2020 28
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2022 35
2023 22
2024 10

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733 results

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Page 1
Amyotrophic lateral sclerosis.
Hardiman O, Al-Chalabi A, Chio A, Corr EM, Logroscino G, Robberecht W, Shaw PJ, Simmons Z, van den Berg LH. Hardiman O, et al. Nat Rev Dis Primers. 2017 Oct 5;3:17071. doi: 10.1038/nrdp.2017.71. Nat Rev Dis Primers. 2017. PMID: 28980624 Free article. Review.
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease, is characterized by the degeneration of both upper and lower motor neurons, which leads to muscle weakness and eventual paralysis. ...Two possible disease-modifying therapies that can sl …
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease, is characterized by the degeneration of both upper and lower …
Cerebral palsy.
Wimalasundera N, Stevenson VL. Wimalasundera N, et al. Pract Neurol. 2016 Jun;16(3):184-94. doi: 10.1136/practneurol-2015-001184. Epub 2016 Feb 2. Pract Neurol. 2016. PMID: 26837375 Review.
Cerebral palsy has always been known as a disorder of movement and posture resulting from a non-progressive injury to the developing brain; however, more recent definitions allow clinicians to appreciate more than just the movement disorder. ...
Cerebral palsy has always been known as a disorder of movement and posture resulting from a non-progressive injury to the developing …
[Amyotrophic lateral sclerosis (ALS) - diagnosis, course of disease and treatment options].
Meyer T. Meyer T. Dtsch Med Wochenschr. 2021 Dec;146(24-25):1613-1618. doi: 10.1055/a-1562-7882. Epub 2021 Dec 8. Dtsch Med Wochenschr. 2021. PMID: 34879411 Review. German.
Amyotrophic lateral sclerosis (ALS) is an adult-onset motor neuron disorder which is characterized by progressive motor symptoms, such as muscle weakness, muscle atrophy and spasticity. ...Genetic factors may be involved even without a family history o …
Amyotrophic lateral sclerosis (ALS) is an adult-onset motor neuron disorder which is characterized by progressive motor symptoms, suc …
Exercise prescription for patients with multiple sclerosis; potential benefits and practical recommendations.
Halabchi F, Alizadeh Z, Sahraian MA, Abolhasani M. Halabchi F, et al. BMC Neurol. 2017 Sep 16;17(1):185. doi: 10.1186/s12883-017-0960-9. BMC Neurol. 2017. PMID: 28915856 Free PMC article. Review.
BACKGROUND: Multiple sclerosis (MS) can result in significant mental and physical symptoms, specially muscle weakness, abnormal walking mechanics, balance problems, spasticity, fatigue, cognitive impairment and depression. ...Flexibility exercises such as stretching …
BACKGROUND: Multiple sclerosis (MS) can result in significant mental and physical symptoms, specially muscle weakness, abnormal walki …
Pathophysiology of spasticity: implications for neurorehabilitation.
Trompetto C, Marinelli L, Mori L, Pelosin E, Currà A, Molfetta L, Abbruzzese G. Trompetto C, et al. Biomed Res Int. 2014;2014:354906. doi: 10.1155/2014/354906. Epub 2014 Oct 30. Biomed Res Int. 2014. PMID: 25530960 Free PMC article. Review.
Spasticity is the velocity-dependent increase in muscle tone due to the exaggeration of stretch reflex. ...An important plastic change in the spinal cord could be the progressive reduction of postactivation depression due to limb immobilization. ...
Spasticity is the velocity-dependent increase in muscle tone due to the exaggeration of stretch reflex. ...An important plasti …
ALS: Management Problems.
Brent JR, Franz CK, Coleman JM 3rd, Ajroud-Driss S. Brent JR, et al. Neurol Clin. 2020 Aug;38(3):565-575. doi: 10.1016/j.ncl.2020.03.013. Epub 2020 Jun 11. Neurol Clin. 2020. PMID: 32703469 Free PMC article. Review.
Amyotrophic lateral sclerosis (ALS) is a fatal disease with no cure; however, symptomatic management has an impact on quality of life and survival. ...Preventing and treating weight loss caused by dysphagia may slow down disease progression, and expert manage …
Amyotrophic lateral sclerosis (ALS) is a fatal disease with no cure; however, symptomatic management has an impact on quality of life …
Amyotrophic lateral sclerosis.
Wijesekera LC, Leigh PN. Wijesekera LC, et al. Orphanet J Rare Dis. 2009 Feb 3;4:3. doi: 10.1186/1750-1172-4-3. Orphanet J Rare Dis. 2009. PMID: 19192301 Free PMC article. Review.
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterised by progressive muscular paralysis reflecting degeneration of motor neurones in the primary motor cortex, corticospinal tracts, brainstem and spinal cord. ...Approximately two thirds of …
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterised by progressive muscular paralysis reflecting …
[Mechanism of action, clinical indication and results of treatment of botulinum toxin].
Lagueny A, Burbaud P. Lagueny A, et al. Neurophysiol Clin. 1996;26(4):216-26. doi: 10.1016/s0987-7053(96)85003-9. Neurophysiol Clin. 1996. PMID: 8975111 Review. French.
Botulinum toxin, the most potent of the neurotoxins, produces paralysis by blocking presynaptic release of the neurotransmitter (acetylcholine) at the neuromuscular junction, with reversible chemical denervation of the muscle fibre, thereby inducing partial paralysis and a …
Botulinum toxin, the most potent of the neurotoxins, produces paralysis by blocking presynaptic release of the neurotransmitter (acetylcholi …
Adult-onset spastic paraparesis: an approach to diagnostic work-up.
Zhovtis Ryerson L, Herbert J, Howard J, Kister I. Zhovtis Ryerson L, et al. J Neurol Sci. 2014 Nov 15;346(1-2):43-50. doi: 10.1016/j.jns.2014.09.015. Epub 2014 Sep 19. J Neurol Sci. 2014. PMID: 25263600 Review.
Adult-onset, chronic progressive spastic paraparesis may be due to a large number of causes and poses a diagnostic challenge. There are no recent evidence-based guidelines or comprehensive reviews to help guide diagnostic work-up. We survey the literature on chronic …
Adult-onset, chronic progressive spastic paraparesis may be due to a large number of causes and poses a diagnostic challenge. …
Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches.
Shribman S, Reid E, Crosby AH, Houlden H, Warner TT. Shribman S, et al. Lancet Neurol. 2019 Dec;18(12):1136-1146. doi: 10.1016/S1474-4422(19)30235-2. Epub 2019 Jul 31. Lancet Neurol. 2019. PMID: 31377012 Review.
Hereditary spastic paraplegia (HSP) describes a heterogeneous group of genetic neurodegenerative diseases characterised by progressive spasticity of the lower limbs. The pathogenic mechanism, associated clinical features, and imaging abnormalities vary substa …
Hereditary spastic paraplegia (HSP) describes a heterogeneous group of genetic neurodegenerative diseases characterised by progres …
733 results