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1988 1
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2004 3
2006 2
2007 5
2008 2
2009 4
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Page 1
Craniosynostosis - Recognition, clinical characteristics, and treatment.
Kajdic N, Spazzapan P, Velnar T. Kajdic N, et al. Bosn J Basic Med Sci. 2018 May 20;18(2):110-116. doi: 10.17305/bjbms.2017.2083. Bosn J Basic Med Sci. 2018. PMID: 28623672 Free PMC article. Review.
The main cause of craniosynostosis is premature closure of one or more cranial sutures. It usually occurs as an isolated condition, but may also be associated with other malformations as part of complex syndromes. ...
The main cause of craniosynostosis is premature closure of one or more cranial sutures. It usually occurs as an isolated condition, b …
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.
Craniosynostosis can result from mutations, chromosomal abnormalities or adverse environmental effects, and can occur in isolation or in association with numerous syndromes. To date, surgical correction remains the primary treatment for craniosynostosis, but it is associat …
Craniosynostosis can result from mutations, chromosomal abnormalities or adverse environmental effects, and can occur in isolation or …
Craniosynostosis.
Governale LS. Governale LS. Pediatr Neurol. 2015 Nov;53(5):394-401. doi: 10.1016/j.pediatrneurol.2015.07.006. Epub 2015 Jul 22. Pediatr Neurol. 2015. PMID: 26371995 Review.
About 8% of the patients have familial or syndromic forms of synostosis, and in the remainder it occurs as a spontaneous isolated defect. Familial craniosynostosis syndromes are typically transmitted as an autosomal dominant trait resulting in disruption of the fibroblast …
About 8% of the patients have familial or syndromic forms of synostosis, and in the remainder it occurs as a spontaneous isolated def …
22q11.2 deletion syndrome and congenital heart disease.
Goldmuntz E. Goldmuntz E. Am J Med Genet C Semin Med Genet. 2020 Mar;184(1):64-72. doi: 10.1002/ajmg.c.31774. Epub 2020 Feb 12. Am J Med Genet C Semin Med Genet. 2020. PMID: 32049433 Review.
New guidelines suggest screening for a 22q11.2 deletion in the patient with tetralogy of Fallot, truncus arteriosus, interrupted aortic arch type B, conoventricular septal defects as well as those with an isolated aortic arch anomaly. Early identification of a 22q11.2 dele …
New guidelines suggest screening for a 22q11.2 deletion in the patient with tetralogy of Fallot, truncus arteriosus, interrupted aortic arch …
Craniofacial anomalies.
Nagy L, Demke JC. Nagy L, et al. Facial Plast Surg Clin North Am. 2014 Nov;22(4):523-48. doi: 10.1016/j.fsc.2014.08.002. Epub 2014 Nov 8. Facial Plast Surg Clin North Am. 2014. PMID: 25444726 Review.
Craniosynostosis, in which 1 or more cranial sutures prematurely fuse, is associated with diverse environmental and genetic factors. Whereas isolated single-suture synostosis is usually sporadic and nonfamilial, FGFR mutations account for most cases of syndromic craniosyno …
Craniosynostosis, in which 1 or more cranial sutures prematurely fuse, is associated with diverse environmental and genetic factors. Whereas …
Management of craniosynostoses.
Renier D, Lajeunie E, Arnaud E, Marchac D. Renier D, et al. Childs Nerv Syst. 2000 Nov;16(10-11):645-58. doi: 10.1007/s003810000320. Childs Nerv Syst. 2000. PMID: 11151714 Review.
Although it is currently thought that surgery is indicated mainly for cosmetic reasons in isolated craniosynostoses, the functional aspects of the treatment must not be underestimated. ...The study of a personal series of 2,137 craniosynostoses shows that the …
Although it is currently thought that surgery is indicated mainly for cosmetic reasons in isolated craniosynostoses, the funct …
Genetics of craniosynostosis.
Kimonis V, Gold JA, Hoffman TL, Panchal J, Boyadjiev SA. Kimonis V, et al. Semin Pediatr Neurol. 2007 Sep;14(3):150-61. doi: 10.1016/j.spen.2007.08.008. Semin Pediatr Neurol. 2007. PMID: 17980312 Review.
Nonsyndromic craniosynostosis is typically an isolated finding that is classified according to the suture(s) involved. Syndromic craniosynostosis is associated with various dysmorphisms involving the face, skeleton, nervous system, and other anomalies and is usually accomp …
Nonsyndromic craniosynostosis is typically an isolated finding that is classified according to the suture(s) involved. Syndromic cran …
Craniosynostosis: Current Evaluation and Management.
Sullivan LE, Li R, Tong VS, Jagasia P, Bonfield CM, Golinko MS, Pontell ME. Sullivan LE, et al. Ann Plast Surg. 2024 Dec 1;93(6S Suppl 3):S144-S149. doi: 10.1097/SAP.0000000000004131. Ann Plast Surg. 2024. PMID: 39527402 Review.
Craniosynostosis is characterized by the premature fusion of one or more cranial sutures, which can lead to abnormal skull shape and restricted skull growth. Although most cases are present in isolation, some are associated with genetic syndromes, such as Pfeiffer, Muenke, …
Craniosynostosis is characterized by the premature fusion of one or more cranial sutures, which can lead to abnormal skull shape and restric …
Genetic advances in craniosynostosis.
Lattanzi W, Barba M, Di Pietro L, Boyadjiev SA. Lattanzi W, et al. Am J Med Genet A. 2017 May;173(5):1406-1429. doi: 10.1002/ajmg.a.38159. Epub 2017 Feb 4. Am J Med Genet A. 2017. PMID: 28160402 Free PMC article. Review.
Craniosynostosis, the premature ossification of one or more skull sutures, is a clinically and genetically heterogeneous congenital anomaly affecting approximately one in 2,500 live births. In most cases, it occurs as an isolated congenital anomaly, that is, nonsyndromic c …
Craniosynostosis, the premature ossification of one or more skull sutures, is a clinically and genetically heterogeneous congenital anomaly …
Consensus: trigonocephaly.
Collmann H, Sörensen N, Krauss J. Collmann H, et al. Childs Nerv Syst. 1996 Nov;12(11):664-8. doi: 10.1007/BF00366148. Childs Nerv Syst. 1996. PMID: 9118128 Review.
Trigonocephaly mostly occurs in isolated synostosis of the metopic suture, but 10-20% of patients are affected by complex syndromes, and in 2-5% the condition is familial. ...
Trigonocephaly mostly occurs in isolated synostosis of the metopic suture, but 10-20% of patients are affected by complex syndromes, …
70 results