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

Year Number of Results
1933 1
1966 1
1970 1
1975 3
1976 1
1977 2
1978 1
1979 1
1980 2
1982 2
1983 1
1986 2
1988 2
1989 2
1990 3
1991 5
1992 3
1993 8
1994 2
1995 12
1996 9
1997 15
1998 8
1999 8
2000 6
2001 5
2002 9
2003 11
2004 6
2005 11
2006 6
2007 15
2008 9
2009 13
2010 16
2011 20
2012 25
2013 19
2014 28
2015 36
2016 38
2017 32
2018 34
2019 42
2020 50
2021 65
2022 56
2023 46
2024 18

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627 results

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Page 1
Craniosynostosis in primary metabolic bone disorders: a single-institution experience.
Punchak MA, Sarris C, Xu E, Flanders TM, Lang SS, Swanson JW, Taylor JA, Heuer GG. Punchak MA, et al. Childs Nerv Syst. 2023 Dec;39(12):3583-3588. doi: 10.1007/s00381-023-06059-z. Epub 2023 Jul 8. Childs Nerv Syst. 2023. PMID: 37420034 Review.
METHODS: Retrospective review of the electronic medical record database was performed to identify patients with primary metabolic bone disorders who underwent craniosynostosis surgery between 2011 and 2022 at a quaternary referral pediatric hospital. Literature revi …
METHODS: Retrospective review of the electronic medical record database was performed to identify patients with primary metabolic bon …
The clinical manifestations, molecular mechanisms and treatment of craniosynostosis.
Stanton E, Urata M, Chen JF, Chai Y. Stanton E, et al. Dis Model Mech. 2022 Apr 1;15(4):dmm049390. doi: 10.1242/dmm.049390. Epub 2022 Apr 22. Dis Model Mech. 2022. PMID: 35451466 Free PMC article. Review.
To date, surgical correction remains the primary treatment for craniosynostosis, but it is associated with complications and with the potential for re-synostosis. ...Here, we provide a comprehensive review of our current understanding of craniosynostosis, inc …
To date, surgical correction remains the primary treatment for craniosynostosis, but it is associated with complications and w …
Primary Delayed Onset Craniosynostosis in a Child With ERF-Related Craniosynostosis Syndrome and Familial Cerebral Cavernous Malformation Syndrome.
Radu S, Jedrzejewski B, Urbinelli L. Radu S, et al. Cleft Palate Craniofac J. 2023 Oct;60(10):1321-1325. doi: 10.1177/10556656221088743. Epub 2022 Mar 21. Cleft Palate Craniofac J. 2023. PMID: 35313736 Review.
Primary delayed onset craniosynostosis is defined as premature suture fusion that developed despite clear radiographic evidence of normal postnatal calvarial configuration and patent sutures earlier in life. It is rare in the literature and typically presents as sec …
Primary delayed onset craniosynostosis is defined as premature suture fusion that developed despite clear radiographic evidenc …
Primary delayed onset craniosynostosis in a child demonstrated by serial computed tomography imaging.
Guevara C, Wallender A, Steinberg B, Ranalli NJ. Guevara C, et al. Int J Oral Maxillofac Surg. 2016 Nov;45(11):1347-1350. doi: 10.1016/j.ijom.2016.05.014. Epub 2016 Jun 5. Int J Oral Maxillofac Surg. 2016. PMID: 27267708 Review.
Primary delayed onset craniosynostosis is a rarely reported phenomenon. ...This case report documents CT demonstrating true primary delayed onset craniosynostosis....
Primary delayed onset craniosynostosis is a rarely reported phenomenon. ...This case report documents CT demonstrating true …
Craniosynostosis: Neonatal Perspectives.
Bautista G. Bautista G. Neoreviews. 2021 Apr;22(4):e250-e257. doi: 10.1542/neo.22-4-e250. Neoreviews. 2021. PMID: 33795400
Primary or congenital craniosynostoses represent the majority of cases and consist of single-suture and multisuture synostoses. Multisuture synostoses are typically associated with distinct craniofacial syndromes, including Muenke syndrome, Apert syndrome, Crouzon s …
Primary or congenital craniosynostoses represent the majority of cases and consist of single-suture and multisuture synostoses …
Primary premature craniosynostosis.
Davidoff E. Davidoff E. Ophthalmic Semin. 1977;2(3):247-82. Ophthalmic Semin. 1977. PMID: 337200 Review. No abstract available.
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.
In this review, we outline the genetic mutations, pathogenesis, and accompanying symptoms underlying syndromic hydrocephalus in the context of: L1 syndrome, syndromic craniosynostoses, achondroplasia, NF 1/2, Down's syndrome, tuberous sclerosis, Walker-Warburg syndrome, …
In this review, we outline the genetic mutations, pathogenesis, and accompanying symptoms underlying syndromic hydrocephalus in the context …
Primary craniosynostosis: imaging features.
Benson ML, Oliverio PJ, Yue NC, Zinreich SJ. Benson ML, et al. AJR Am J Roentgenol. 1996 Mar;166(3):697-703. doi: 10.2214/ajr.166.3.8623653. AJR Am J Roentgenol. 1996. PMID: 8623653
In 1851, Virchow introduced the term craniosynostosis to describe a variety of abnormalities in calvarial growth. ...This pictorial essay illustrates the imaging findings, nomenclature, and associated abnormalities of the various types of primary craniosynostosis …
In 1851, Virchow introduced the term craniosynostosis to describe a variety of abnormalities in calvarial growth. ...This pictorial e …
Genetics of Nonsyndromic Craniosynostosis.
Timberlake AT, Persing JA. Timberlake AT, et al. Plast Reconstr Surg. 2018 Jun;141(6):1508-1516. doi: 10.1097/PRS.0000000000004374. Plast Reconstr Surg. 2018. PMID: 29579021
Nonsyndromic craniosynostosis is sporadic in more than 95 percent of affected families; thus, surgeons have suggested for decades that nonsyndromic craniosynostosis is likely a fluke occurrence. Contrary to this, recent studies have established that genetics underli …
Nonsyndromic craniosynostosis is sporadic in more than 95 percent of affected families; thus, surgeons have suggested for decades tha …
627 results