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

Year Number of Results
1962 1
1963 87
1964 163
1965 101
1966 119
1967 195
1968 219
1969 261
1970 282
1971 359
1972 387
1973 444
1974 514
1975 403
1976 465
1977 435
1978 505
1979 574
1980 592
1981 588
1982 646
1983 827
1984 930
1985 974
1986 1071
1987 1622
1988 2667
1989 3162
1990 3290
1991 3372
1992 3605
1993 3738
1994 3977
1995 3927
1996 4294
1997 4293
1998 4490
1999 4645
2000 5220
2001 5461
2002 5423
2003 6004
2004 6319
2005 6595
2006 7381
2007 7196
2008 7169
2009 6941
2010 7368
2011 7698
2012 8184
2013 8776
2014 8892
2015 8681
2016 9139
2017 9129
2018 8297
2019 7802
2020 11152
2021 11782
2022 10328
2023 9045
2024 3338

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232,591 results

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The following term was not found in PubMed: Neurofacioskeletal
Page 1
Neuromuscular hyperexcitability syndromes.
De Wel B, Claeys KG. De Wel B, et al. Curr Opin Neurol. 2021 Oct 1;34(5):714-720. doi: 10.1097/WCO.0000000000000963. Curr Opin Neurol. 2021. PMID: 34914668 Review.
PURPOSE OF REVIEW: To provide an update on recent developments regarding acquired, antibody-mediated, neuromuscular hyperexcitability syndromes, including Isaac's and Morvan's syndromes, cramp-fasciculation syndrome and rippling muscle disease, and their gene …
PURPOSE OF REVIEW: To provide an update on recent developments regarding acquired, antibody-mediated, neuromuscular hyperexcitability syn …
VEXAS Syndrome-A Review of Pathophysiology, Presentation, and Prognosis.
Koster MJ, Samec MJ, Warrington KJ. Koster MJ, et al. J Clin Rheumatol. 2023 Sep 1;29(6):298-306. doi: 10.1097/RHU.0000000000001905. Epub 2022 Oct 17. J Clin Rheumatol. 2023. PMID: 36251488 Review.
VEXAS ( V acuoles, E 1 enzyme, X -linked, A utoinflammatory, S omatic) syndrome is a newly identified disease caused by somatic mutations in the UBA1 gene resulting in refractory autoinflammatory features, frequently accompanied by cytopenias. Although the prevalence of th …
VEXAS ( V acuoles, E 1 enzyme, X -linked, A utoinflammatory, S omatic) syndrome is a newly identified disease caused by somatic mutat …
[VEXAS syndrome].
Zeeck M, Kötter I, Krusche M. Zeeck M, et al. Z Rheumatol. 2022 Nov;81(9):782-786. doi: 10.1007/s00393-022-01169-6. Epub 2022 Feb 18. Z Rheumatol. 2022. PMID: 35179640 Free PMC article. Review. German.
The VEXAS syndrome is a recently identified autoinflammatory systemic disease. ...The patients present with a plethora of inflammatory clinical symptoms, often with overlap of hematologic, dermatologic, and rheumatologic syndromes. In particular, the presence of cyt …
The VEXAS syndrome is a recently identified autoinflammatory systemic disease. ...The patients present with a plethora of inflammator …
Neurovascular Syndromes.
Keith KA, Reed LK, Nguyen A, Qaiser R. Keith KA, et al. Neurosurg Clin N Am. 2022 Jan;33(1):135-148. doi: 10.1016/j.nec.2021.09.010. Neurosurg Clin N Am. 2022. PMID: 34801137 Review.
Patients with cerebrovascular syndromes are at risk for additional concerns associated with their syndrome. ...Precise diagnosis and appreciation for the underlying syndrome is critical for effective cerebrovascular and broader care. ...
Patients with cerebrovascular syndromes are at risk for additional concerns associated with their syndrome. ...Precise diagnos …
Sunflower syndrome: a poorly understood photosensitive epilepsy.
Geenen KR, Patel S, Thiele EA. Geenen KR, et al. Dev Med Child Neurol. 2021 Mar;63(3):259-262. doi: 10.1111/dmcn.14723. Epub 2020 Oct 31. Dev Med Child Neurol. 2021. PMID: 33135153 Free article. Review.
Sunflower syndrome is a rare photosensitive epilepsy which has received little attention in recent medical literature. ...Further study is required to determine the syndrome's natural history and to identify more effective treatment options. ...
Sunflower syndrome is a rare photosensitive epilepsy which has received little attention in recent medical literature. ...Further stu …
Hemangioma-related syndromes.
Valdebran M, Wine Lee L. Valdebran M, et al. Curr Opin Pediatr. 2020 Aug;32(4):498-505. doi: 10.1097/MOP.0000000000000925. Curr Opin Pediatr. 2020. PMID: 32692048 Review.
The current review will discuss recent clinical advances in syndromes associated with segmental hemangiomas, including PHACE and LUMBAR syndrome. ...Segmental hemangiomas of the head and neck region may indicate a risk of PHACE syndrome and associated develop …
The current review will discuss recent clinical advances in syndromes associated with segmental hemangiomas, including PHACE and LUMB …
Syndromic Hydrocephalus.
Varagur K, Sanka SA, Strahle JM. Varagur K, et al. Neurosurg Clin N Am. 2022 Jan;33(1):67-79. doi: 10.1016/j.nec.2021.09.006. Neurosurg Clin N Am. 2022. PMID: 34801143 Free PMC article. Review.
Hydrocephalus, the abnormal accumulation and impaired circulation/clearance of cerebrospinal fluid, occurs as a common phenotypic feature of a diverse group of genetic syndromes. In this review, we outline the genetic mutations, pathogenesis, and accompanying symptoms unde …
Hydrocephalus, the abnormal accumulation and impaired circulation/clearance of cerebrospinal fluid, occurs as a common phenotypic feature of …
[Dystonia].
Løkkegaard A, Danielsen EH. Løkkegaard A, et al. Ugeskr Laeger. 2019 May 13;181(20):V06180403. Ugeskr Laeger. 2019. PMID: 31124448 Free article. Review. Danish.
Dystonia is a rare and heterogeneous movement disorder defined as a syn-drome of sustained muscle contractions with twisting and abnormal postures, and tremor. Dystonia is a collective term for different syndromes, primary idiopathic forms as well as genetic and secondary …
Dystonia is a rare and heterogeneous movement disorder defined as a syn-drome of sustained muscle contractions with twisting and abnormal po …
Clinical approach to neuro-rheumatology.
Goglin S, Cho TA. Goglin S, et al. J Neurol Sci. 2021 Dec 15;431:120048. doi: 10.1016/j.jns.2021.120048. Epub 2021 Nov 6. J Neurol Sci. 2021. PMID: 34768134 Review.
Using a systematic approach allows the clinician to diagnose these conditions more readily and to initiate treatment more rapidly. Specific neurological syndromes frequently associated with rheumatologic or specific autoimmune conditions can suggest the diagnosis. ...Judic …
Using a systematic approach allows the clinician to diagnose these conditions more readily and to initiate treatment more rapidly. Specific …
Molecular Mechanisms Involved in Craniosynostosis.
Yapijakis C, Pachis N, Sotiriadou T, Vaila C, Michopoulou V, Vassiliou S. Yapijakis C, et al. In Vivo. 2023 Jan-Feb;37(1):36-46. doi: 10.21873/invivo.13052. In Vivo. 2023. PMID: 36593018 Free PMC article. Review.
In most cases (85%), craniosynostosis is presented as sporadic anomaly (non-syndromic craniosynostosis), while in other cases (15%) as part of syndromes (syndromic craniosynostosis). ...Most common syndromes of craniosynostosis include Pfeiffer, Apert, …
In most cases (85%), craniosynostosis is presented as sporadic anomaly (non-syndromic craniosynostosis), while in other cases (15%) a …
232,591 results
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