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

Year Number of Results
1971 1
1972 1
1973 1
1975 5
1976 5
1977 3
1978 10
1979 3
1980 4
1981 5
1982 4
1983 5
1984 6
1985 14
1986 5
1987 7
1988 6
1989 5
1990 14
1991 17
1992 14
1993 23
1994 25
1995 25
1996 18
1997 28
1998 32
1999 33
2000 27
2001 22
2002 23
2003 41
2004 33
2005 31
2006 46
2007 39
2008 60
2009 52
2010 48
2011 47
2012 46
2013 48
2014 75
2015 89
2016 76
2017 93
2018 86
2019 76
2020 58
2021 51
2022 26
2023 22
2024 8

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1,369 results

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Quoted phrase not found in phrase index: "Abnormal spinal cord physiology"
Page 1
Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy: A Review of the Literature.
Shan F, Long Y, Qiu W. Shan F, et al. Front Immunol. 2018 Dec 5;9:2802. doi: 10.3389/fimmu.2018.02802. eCollection 2018. Front Immunol. 2018. PMID: 30568655 Free PMC article. Review.
GFAP autoantibody, especially IgG that binds to GFAPalpha, has been reported in the cerebrospinal fluid (CSF) and serum of patients with GFAP astrocytopathy. The positive predictive value of GFAP antibody in the CSF is higher than in the serum. ...Clinical manifestations i …
GFAP autoantibody, especially IgG that binds to GFAPalpha, has been reported in the cerebrospinal fluid (CSF) and serum of patients with GFA …
MRI characteristics of neuromyelitis optica spectrum disorder: an international update.
Kim HJ, Paul F, Lana-Peixoto MA, Tenembaum S, Asgari N, Palace J, Klawiter EC, Sato DK, de Seze J, Wuerfel J, Banwell BL, Villoslada P, Saiz A, Fujihara K, Kim SH; Guthy-Jackson Charitable Foundation NMO International Clinical Consortium & Biorepository. Kim HJ, et al. Neurology. 2015 Mar 17;84(11):1165-73. doi: 10.1212/WNL.0000000000001367. Epub 2015 Feb 18. Neurology. 2015. PMID: 25695963 Free PMC article. Review.
Some seropositive patients present with brain involvement during their first attack and/or continue to relapse in the same location without optic nerve and spinal cord involvement. Thus, characteristics of brain abnormalities in such patients have become of i …
Some seropositive patients present with brain involvement during their first attack and/or continue to relapse in the same location without …
Anorectal malformations.
Levitt MA, Peña A. Levitt MA, et al. Orphanet J Rare Dis. 2007 Jul 26;2:33. doi: 10.1186/1750-1172-2-33. Orphanet J Rare Dis. 2007. PMID: 17651510 Free PMC article. Review.
Better imaging techniques, and a better knowledge of the anatomy and physiology of the pelvic structures at birth have refined diagnosis and initial management, and the analysis of large series of patients allows better prediction of associated anomalies and functio …
Better imaging techniques, and a better knowledge of the anatomy and physiology of the pelvic structures at birth have refined diagno …
Natural history of spinal cavernous malformations.
Otten M, Mccormick P. Otten M, et al. Handb Clin Neurol. 2017;143:233-239. doi: 10.1016/B978-0-444-63640-9.00022-9. Handb Clin Neurol. 2017. PMID: 28552145 Review.
Spinal cavernous malformations are intramedullary vascular lesions. ...Characteristics that correlated with better neurologic outcome were: resection within 3 months of the onset of symptoms, gross total resection, presentation with motor symptoms, and an acute course …
Spinal cavernous malformations are intramedullary vascular lesions. ...Characteristics that correlated with better neurologic outcome …
Somatic MAP3K3 and PIK3CA mutations in sporadic cerebral and spinal cord cavernous malformations.
Hong T, Xiao X, Ren J, Cui B, Zong Y, Zou J, Kou Z, Jiang N, Meng G, Zeng G, Shan Y, Wu H, Chen Z, Liang J, Xiao X, Tang J, Wei Y, Ye M, Sun L, Li G, Hu P, Hui R, Zhang H, Wang Y. Hong T, et al. Brain. 2021 Oct 22;144(9):2648-2658. doi: 10.1093/brain/awab117. Brain. 2021. PMID: 33729480

The mutation spectrum correlated with lesion size (P = 0.001), anatomical distribution (P < 0.001), MRI appearance (P = 0.004) and haemorrhage events (P = 0.006). PIK3CA mutation was a significant predictor of overt haemorrhage events (P = 0.003, odds ratio = 11.252, 95

…

The mutation spectrum correlated with lesion size (P = 0.001), anatomical distribution (P < 0.001), MRI appearance (P = 0.004) and haemor

…
What role should spinal cord MRI take in the future of multiple sclerosis surveillance?
Rocca MA, Preziosa P, Filippi M. Rocca MA, et al. Expert Rev Neurother. 2020 Aug;20(8):783-797. doi: 10.1080/14737175.2020.1739524. Epub 2020 Mar 25. Expert Rev Neurother. 2020. PMID: 32133874 Review.
Although spinal cord imaging may be challenging, improvements in MRI technologies have contributed to better evaluate spinal cord involvement in MS. ...The role of spinal cord atrophy and of other advanced MRI techniques to better evaluat …
Although spinal cord imaging may be challenging, improvements in MRI technologies have contributed to better evaluate spina …
Central nervous system vascular malformations: A clinical review.
Sabayan B, Lineback C, Viswanathan A, Leslie-Mazwi TM, Shaibani A. Sabayan B, et al. Ann Clin Transl Neurol. 2021 Feb;8(2):504-522. doi: 10.1002/acn3.51277. Epub 2021 Jan 12. Ann Clin Transl Neurol. 2021. PMID: 33434339 Free PMC article. Review.
This range spans lesions with a risk of devastating neurological compromise to lesions with a slow, static or benign course. Advances in neurovascular imaging along with increased utilization of these advances, have resulted in more frequent identification of these lesions …
This range spans lesions with a risk of devastating neurological compromise to lesions with a slow, static or benign course. Advances …
Neuro-osteology.
Kjaer I. Kjaer I. Crit Rev Oral Biol Med. 1998;9(2):224-44. doi: 10.1177/10454411980090020501. Crit Rev Oral Biol Med. 1998. PMID: 9603237 Review.
Also, abnormal development in the craniofacial region, such as tooth agenesis, is analyzed neuro-osteologically. Results from pre-natal investigations provide information on the post-natal diagnosis of children with congenital developmental disorders in the central …
Also, abnormal development in the craniofacial region, such as tooth agenesis, is analyzed neuro-osteologically. Results from pre-nat …
Arthrogryposis multiplex congenita.
Gordon N. Gordon N. Brain Dev. 1998 Oct;20(7):507-11. doi: 10.1016/s0387-7604(98)00037-0. Brain Dev. 1998. PMID: 9840670 Review.
The common factor causing congenital arthrogryposis is lack of fetal movements. This can result from a large number of disorders. They may be neuropathic, affecting the brain, the spinal cord, or the peripheral nerves; they may be abnormalities of the …
The common factor causing congenital arthrogryposis is lack of fetal movements. This can result from a large number of disorders. The …
Spinal dural arteriovenous fistula.
Koch C. Koch C. Curr Opin Neurol. 2006 Feb;19(1):69-75. doi: 10.1097/01.wco.0000200547.22292.11. Curr Opin Neurol. 2006. PMID: 16415680 Review.
PURPOSE OF REVIEW: To summarize clinical key points, diagnostic features, and results of imaging and therapy of spinal dural arteriovenous fistula (SDAVF). RECENT FINDINGS: SDAVF accounts for 70% of spinal arteriovenous malformation with an annual incidence of 5-10 …
PURPOSE OF REVIEW: To summarize clinical key points, diagnostic features, and results of imaging and therapy of spinal dural arteriov …
1,369 results