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
1975 1
1976 1
1977 3
1979 1
1980 1
1982 2
1984 2
1985 1
1986 2
1987 1
1989 3
1990 1
1991 2
1992 4
1993 2
1994 3
1995 6
1996 8
1997 2
1998 5
1999 7
2000 5
2001 9
2002 6
2003 5
2004 7
2005 9
2006 4
2007 14
2008 9
2009 9
2010 7
2011 15
2012 20
2013 11
2014 8
2015 16
2016 13
2017 18
2018 12
2019 16
2020 16
2021 24
2022 19
2023 21
2024 7

Text availability

Article attribute

Article type

Publication date

Search Results

323 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormality of cranial sutures"
Page 1
Nonsyndromic Craniosynostosis.
Dempsey RF, Monson LA, Maricevich RS, Truong TA, Olarunnipa S, Lam SK, Dauser RC, Hollier LH Jr, Buchanan EP. Dempsey RF, et al. Clin Plast Surg. 2019 Apr;46(2):123-139. doi: 10.1016/j.cps.2018.11.001. Epub 2019 Jan 30. Clin Plast Surg. 2019. PMID: 30851746 Review.
Nonsyndromic craniosynostosis is significantly more common than syndromic craniosynostosis, affecting the sagittal, coronal, metopic, and lambdoid sutures in decreasing order of frequency. Nonsyndromic craniosynostosis is most frequently associated with only 1 fused suture …
Nonsyndromic craniosynostosis is significantly more common than syndromic craniosynostosis, affecting the sagittal, coronal, metopic, and la …
Cranial sutures.
Ganz JC. Ganz JC. Prog Brain Res. 2024;285:127-136. doi: 10.1016/bs.pbr.2024.02.019. Epub 2024 Apr 25. Prog Brain Res. 2024. PMID: 38705712
Cranial sutures are not of great concern to the modern neurosurgeon, except when abnormalities interfere with the skull's shape and its ability to expand during childhood. ...Galen for reasons that are far from clear, "observed" relationships between t
Cranial sutures are not of great concern to the modern neurosurgeon, except when abnormalities interfere with the skull
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.
Craniosynostosis refers to the early fusion of one or many cranial sutures, causing craniofacial abnormalities observed in 1:2,500 births worldwide. ...The main gene mutations in craniosynostosis involve FGFR1, FGFR2, FGFR3, TWIST1 and MSX2, which enco …
Craniosynostosis refers to the early fusion of one or many cranial sutures, causing craniofacial abnormalities obser
Pycnodysostosis at otorhinolaryngology.
Baglam T, Binnetoglu A, Fatih Topuz M, Baş Ikizoglu N, Ersu R, Turan S, Sarı M. Baglam T, et al. Int J Pediatr Otorhinolaryngol. 2017 Apr;95:91-96. doi: 10.1016/j.ijporl.2017.02.009. Epub 2017 Feb 11. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28576543
Pycnodysostosis is characterized by short stature, characteristic facial appearance (delayed closure of fontanelles and cranial sutures, mandibular hypoplasia and angle disorder, blue sclera), and acroosteolysis of the distal phalanges. ...One patient (12.5%) had gr …
Pycnodysostosis is characterized by short stature, characteristic facial appearance (delayed closure of fontanelles and cranial su
A Genetic-Pathophysiological Framework for Craniosynostosis.
Twigg SR, Wilkie AO. Twigg SR, et al. Am J Hum Genet. 2015 Sep 3;97(3):359-77. doi: 10.1016/j.ajhg.2015.07.006. Am J Hum Genet. 2015. PMID: 26340332 Free PMC article. Review.
Craniosynostosis, the premature fusion of one or more cranial sutures of the skull, provides a paradigm for investigating the interplay of genetic and environmental factors leading to malformation. ...In parallel, however, we need a pathogenetic classification to de …
Craniosynostosis, the premature fusion of one or more cranial sutures of the skull, provides a paradigm for investigating the …
The foramen magnum in scaphocephaly.
Skadorwa T, Wierzbieniec O. Skadorwa T, et al. Childs Nerv Syst. 2022 Nov;38(11):2163-2170. doi: 10.1007/s00381-022-05624-2. Epub 2022 Aug 5. Childs Nerv Syst. 2022. PMID: 35931858 Free PMC article.
However, to date, no study has been devoted to its morphology and morphometry in scaphocephaly, which is the most common of cranial deformities resulting from premature fusion of cranial sutures. ...RESULTS: Dolichotrematous type of FM was dominant in the sca …
However, to date, no study has been devoted to its morphology and morphometry in scaphocephaly, which is the most common of cranial d …
Determining the fate of cranial sutures after surgical correction of non-syndromic craniosynostosis.
Kim SY, Shin HJ, Lim SY. Kim SY, et al. J Craniomaxillofac Surg. 2017 Nov;45(11):1801-1808. doi: 10.1016/j.jcms.2017.08.009. Epub 2017 Aug 19. J Craniomaxillofac Surg. 2017. PMID: 28939204 Review.
PURPOSE: "Secondary craniosynostosis" (SCS) refers to a loss of sutures after corrective vault reconstruction. There are no prior studies that comprehensively review SCS in various types of non-syndromic craniosynostosis. ...A literature search of the Medline and Ovid data …
PURPOSE: "Secondary craniosynostosis" (SCS) refers to a loss of sutures after corrective vault reconstruction. There are no prior stu …
Non-syndromic craniosynostosis in children: Scoping review.
Garrocho-Rangel A, Manriquez-Olmos L, Flores-Velazquez J, Rosales-Berber MA, Martinez-Rider R, Pozos-Guillen A. Garrocho-Rangel A, et al. Med Oral Patol Oral Cir Bucal. 2018 Jul 1;23(4):e421-e428. doi: 10.4317/medoral.22328. Med Oral Patol Oral Cir Bucal. 2018. PMID: 29924758 Free PMC article. Review.
BACKGROUND: Craniosynostosis (CS) is a complex condition consisting of the early fusion of one or more cranial sutures in the intrauterine stage. The affected infant exhibits abnormal head shape at time of birth or shortly thereafter. It can be observed
BACKGROUND: Craniosynostosis (CS) is a complex condition consisting of the early fusion of one or more cranial sutures in the …
Ciliary Signalling and Mechanotransduction in the Pathophysiology of Craniosynostosis.
Tiberio F, Parolini O, Lattanzi W. Tiberio F, et al. Genes (Basel). 2021 Jul 14;12(7):1073. doi: 10.3390/genes12071073. Genes (Basel). 2021. PMID: 34356089 Free PMC article. Review.
Craniosynostosis (CS) is the second most prevalent inborn craniofacial malformation; it results from the premature fusion of cranial sutures and leads to dimorphisms of variable severity. CS is clinically heterogeneous, as it can be either a sporadic isolated defect …
Craniosynostosis (CS) is the second most prevalent inborn craniofacial malformation; it results from the premature fusion of cranial
Understanding craniosynostosis as a growth disorder.
Flaherty K, Singh N, Richtsmeier JT. Flaherty K, et al. Wiley Interdiscip Rev Dev Biol. 2016 Jul;5(4):429-59. doi: 10.1002/wdev.227. Epub 2016 Mar 22. Wiley Interdiscip Rev Dev Biol. 2016. PMID: 27002187 Free PMC article. Review.
Craniosynostosis is a condition of complex etiology that always involves the premature fusion of one or multiple cranial sutures and includes various anomalies of the soft and hard tissues of the head. ...Identification of these genetic mutations has allowed signifi …
Craniosynostosis is a condition of complex etiology that always involves the premature fusion of one or multiple cranial sutures
323 results