Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1967 1
1968 1
1969 1
1970 1
1972 1
1974 2
1975 2
1976 3
1980 1
1981 1
1984 2
1985 1
1987 2
1988 6
1989 9
1990 8
1991 6
1992 9
1993 7
1994 13
1995 13
1996 10
1997 12
1998 12
1999 12
2000 13
2001 14
2002 15
2003 7
2004 14
2005 12
2006 11
2007 14
2008 15
2009 17
2010 13
2011 15
2012 17
2013 15
2014 20
2015 20
2016 13
2017 16
2018 15
2019 14
2020 16
2021 13
2022 12
2023 10
2024 4

Text availability

Article attribute

Article type

Publication date

Search Results

431 results

Results by year

Filters applied: . Clear all
Page 1
Klippel-Feil syndrome: a review of the literature.
Frikha R. Frikha R. Clin Dysmorphol. 2020 Jan;29(1):35-37. doi: 10.1097/MCD.0000000000000301. Clin Dysmorphol. 2020. PMID: 31577545 Review.
Klippel-Feil syndrome is a congenital defect in the formation or segmentation of the cervical spine. ...This heterogeneity has complicated clarification of the genetic causes and management of patient's with congenital vertebral fusion. In this review, …
Klippel-Feil syndrome is a congenital defect in the formation or segmentation of the cervical spine. ...This heterogene …
Ischemic Stroke in the Young.
Berkman SA, Song SS. Berkman SA, et al. Clin Appl Thromb Hemost. 2021 Jan-Dec;27:10760296211002274. doi: 10.1177/10760296211002274. Clin Appl Thromb Hemost. 2021. PMID: 33870763 Free PMC article. Review.
Cervicothoracic cystic dysraphism.
Valeur NS, Iyer RS, Ishak GE. Valeur NS, et al. Pediatr Radiol. 2016 Sep;46(10):1471-81. doi: 10.1007/s00247-016-3632-9. Epub 2016 May 5. Pediatr Radiol. 2016. PMID: 27147079 Review.
Cystic dysraphism of the cervical and upper thoracic spine is very rare. It differs from the much more common lumbosacral dysraphism in appearance and structure, and usually portends a better prognosis due to lack of functional neurological tissue in the dysraphic s …
Cystic dysraphism of the cervical and upper thoracic spine is very rare. It differs from the much more common lumbosacral dysr …
Anterocollis and anterocaput.
Finsterer J, Revuelta GJ. Finsterer J, et al. Clin Neurol Neurosurg. 2014 Dec;127:44-53. doi: 10.1016/j.clineuro.2014.09.020. Epub 2014 Oct 2. Clin Neurol Neurosurg. 2014. PMID: 25459242 Review.
Anterocollis/anterocaput is a subtype of cervical dystonia and the most infrequent of its abnormal head-positions. Anterocollis can be differentiated from anterocaput by the abnormal angle between thoracic and cervical spine or between skull-bas …
Anterocollis/anterocaput is a subtype of cervical dystonia and the most infrequent of its abnormal head-positions. Anterocolli …
Cervical Vertigo: Historical Reviews and Advances.
Peng B. Peng B. World Neurosurg. 2018 Jan;109:347-350. doi: 10.1016/j.wneu.2017.10.063. Epub 2017 Oct 20. World Neurosurg. 2018. PMID: 29061460 Review.
Vertigo is one of the most common presentations in adult patients. Among the various causes of vertigo, so-called cervical vertigo is still a controversial entity. Cervical vertigo was first thought to be due to abnormal input from cervical sympathetic …
Vertigo is one of the most common presentations in adult patients. Among the various causes of vertigo, so-called cervical vertigo is …
Adult cervical deformity: radiographic and osteotomy classifications.
Diebo BG, Shah NV, Solow M, Challier V, Paulino CB, Passias PG, Lafage R, Schwab FJ, Kim HJ, Lafage V. Diebo BG, et al. Orthopade. 2018 Jun;47(6):496-504. doi: 10.1007/s00132-018-3581-0. Orthopade. 2018. PMID: 29881915 Review. English.
Cervical spine deformity represents a broad spectrum of pathologies that are both complex in etiology and debilitating towards quality of life for patients. Despite advances in the understanding of drivers and outcomes of cervical spine deformity, only
Cervical spine deformity represents a broad spectrum of pathologies that are both complex in etiology and debilitating towards
Cervical spine anomalies in children and adolescents.
Kim HJ. Kim HJ. Curr Opin Pediatr. 2013 Feb;25(1):72-7. doi: 10.1097/MOP.0b013e32835bd4cf. Curr Opin Pediatr. 2013. PMID: 23263023 Review.
PURPOSE OF REVIEW: Cervical spine anomalies in paediatric patients are difficult to recognize due to the unique anatomy of the developing spine as well as the rarity of their occurrence. ...SUMMARY: Due to the unique anatomy of the cervical
PURPOSE OF REVIEW: Cervical spine anomalies in paediatric patients are difficult to recognize due to the unique anatomy
Review of cervical spine anomalies in genetic syndromes.
McKay SD, Al-Omari A, Tomlinson LA, Dormans JP. McKay SD, et al. Spine (Phila Pa 1976). 2012 Mar 1;37(5):E269-77. doi: 10.1097/BRS.0b013e31823b3ded. Spine (Phila Pa 1976). 2012. PMID: 22045003 Review.
STUDY DESIGN: Focused review of the literature. OBJECTIVE: Assist spine specialists in diagnosis and treatment of cervical spine anomalies found in selected genetic syndromes. SUMMARY OF BACKGROUND DATA: Cervical spine instability and/or stenosi …
STUDY DESIGN: Focused review of the literature. OBJECTIVE: Assist spine specialists in diagnosis and treatment of cervical
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Peluso F, Caraffi SG, Contrò G, Valeri L, Napoli M, Carboni G, Seth A, Zuntini R, Coccia E, Astrea G, Bisgaard AM, Ivanovski I, Maitz S, Brischoux-Boucher E, Carter MT, Dentici ML, Devriendt K, Bellini M, Digilio MC, Doja A, Dyment DA, Farholt S, Ferreira CR, Wolfe LA, Gahl WA, Gnazzo M, Goel H, Grønborg SW, Hammer T, Iughetti L, Kleefstra T, Koolen DA, Lepri FR, Lemire G, Louro P, McCullagh G, Madeo SF, Milone A, Milone R, Nielsen JEK, Novelli A, Ockeloen CW, Pascarella R, Pippucci T, Ricca I, Robertson SP, Sawyer S, Falkenberg Smeland M, Stegmann S, Stumpel CT, Goel A, Taylor JM, Barbuti D, Soresina A, Bedeschi MF, Battini R, Cavalli A, Fusco C, Iascone M, Van Maldergem L, Venkateswaran S, Zuffardi O, Vergano S, Garavelli L, Bayat A. Peluso F, et al. J Med Genet. 2023 Nov 27;60(12):1224-1234. doi: 10.1136/jmg-2023-109141. J Med Genet. 2023. PMID: 37586838 Free PMC article. Review.
We found no correlation between these structural anomalies and epilepsy or intellectual disability. Prevalent skeletal findings comprised abnormalities of the spine including scoliosis, coccygeal anomalies and cervical ribs. Hand X-rays revealed frequent a
We found no correlation between these structural anomalies and epilepsy or intellectual disability. Prevalent skeletal findings comprised …
A Review of Spinal Lesions in Neurofibromatosis Type 1 in a Large Neurofibromatosis Type 1 Center.
Sial M, George KJ. Sial M, et al. World Neurosurg. 2023 Jan;169:e157-e163. doi: 10.1016/j.wneu.2022.10.100. Epub 2022 Nov 2. World Neurosurg. 2023. PMID: 36334707 Review.
RESULTS: Four-hundred forty-seven patients had classic NF1, and 67 patients had spinal NF1. Many of the patients had spinal abnormalities; 25.7% of these patients were found to have dural ectasia, whereas 44.9% of patients had a spinal deformity. ...The patients with spina …
RESULTS: Four-hundred forty-seven patients had classic NF1, and 67 patients had spinal NF1. Many of the patients had spinal abnormalities
431 results