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

Year Number of Results
1967 1
1968 3
1969 1
1971 1
1972 3
1974 1
1975 2
1977 1
1978 1
1979 2
1980 1
1981 6
1982 1
1985 6
1987 2
1988 10
1989 4
1990 10
1991 23
1992 6
1993 17
1994 21
1995 26
1996 22
1997 29
1998 20
1999 16
2000 29
2001 23
2002 21
2003 15
2004 19
2005 27
2006 30
2007 25
2008 27
2009 13
2010 26
2011 25
2012 46
2013 27
2014 31
2015 32
2016 35
2017 32
2018 39
2019 44
2020 23
2021 43
2022 42
2023 35
2024 7

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883 results

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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.
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped skull. ...Thus, early diagnosis, expert surgical techniques, postoperative care, and adequate follow-up are of vital importance in treating crani …
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped skull. . …
Anaesthesia of brachycephalic dogs.
Downing F, Gibson S. Downing F, et al. J Small Anim Pract. 2018 Dec;59(12):725-733. doi: 10.1111/jsap.12948. Epub 2018 Oct 29. J Small Anim Pract. 2018. PMID: 30374971 Review.
These breeds are predisposed to several conditions, notably brachycephalic obstructive airway syndrome and gastro-oesophageal reflux, that have important implications for anaesthetic management and carry high risk for complications. ...We focus on preoperative identificati …
These breeds are predisposed to several conditions, notably brachycephalic obstructive airway syndrome and gastro-oesophageal reflux, …
Positional Plagiocephaly and Craniosynostosis.
Santiago GS, Santiago CN, Chwa ES, Purnell CA. Santiago GS, et al. Pediatr Ann. 2023 Jan;52(1):e10-e17. doi: 10.3928/19382359-20221114-03. Epub 2023 Jan 1. Pediatr Ann. 2023. PMID: 36625797 Review.
Along with the decrease in sudden infant death syndrome due to the successful "Back to Sleep" Campaign, there was a reciprocal increase in cases of positional plagiocephaly (PP). ...This review explores the causes, risk factors, and treatment options of PP and craniosyn …
Along with the decrease in sudden infant death syndrome due to the successful "Back to Sleep" Campaign, there was a reciprocal increa …
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 is a major congenital craniofacial disorder characterized by the premature fusion of cranial suture(s). ...Here, we provide a comprehensive review of our current understanding of craniosynostosis, including typical craniosynostosis types, the …
Craniosynostosis is a major congenital craniofacial disorder characterized by the premature fusion of cranial suture(s). ...Here, we …
Syndromic Craniosynostosis.
Sawh-Martinez R, Steinbacher DM. Sawh-Martinez R, et al. Clin Plast Surg. 2019 Apr;46(2):141-155. doi: 10.1016/j.cps.2018.11.009. Clin Plast Surg. 2019. PMID: 30851747 Review.
The most common craniosynostosis syndromes include Apert (FGFR2), Crouzon (FGFR2), Muenke (FGFR3), Pfeiffer (FGFR1 and FGFR2), and Saethre-Chotzen (TWIST). Bicoronal craniosynostosis (turribrachycephaly) is most commonly associated with syndromic craniosynostosis …
The most common craniosynostosis syndromes include Apert (FGFR2), Crouzon (FGFR2), Muenke (FGFR3), Pfeiffer (FGFR1 and FGFR2), and Sa …
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.
The 22q11.2 deletion syndrome has an estimated prevalence of 1 in 4-6,000 livebirths. The phenotype varies widely; the most common features include: facial dysmorphia, hypocalcemia, palate and speech disorders, feeding and gastrointestinal disorders, immunodeficiency, recu …
The 22q11.2 deletion syndrome has an estimated prevalence of 1 in 4-6,000 livebirths. The phenotype varies widely; the most common fe …
Craniosynostosis and ENT.
Couloigner V, Ayari Khalfallah S. Couloigner V, et al. Neurochirurgie. 2019 Nov;65(5):318-321. doi: 10.1016/j.neuchi.2019.09.015. Epub 2019 Sep 27. Neurochirurgie. 2019. PMID: 31568777 Review.
OBJECTIVE: The aim of the present study was to review the literature on ENT disorders associated with craniosynostosis (CS), focusing on symptoms, diagnostic work-up, treatment and outcome. METHODS: Publications were retrieved by consulting the PubMed free search engine of …
OBJECTIVE: The aim of the present study was to review the literature on ENT disorders associated with craniosynostosis (CS), focusing …
Craniosynostosis.
Nagaraja S, Anslow P, Winter B. Nagaraja S, et al. Clin Radiol. 2013 Mar;68(3):284-92. doi: 10.1016/j.crad.2012.07.005. Epub 2012 Aug 28. Clin Radiol. 2013. PMID: 22939693 Review.
Craniosynostosis is a complex condition, characterized by the premature fusion of one of more of the cranial sutures. ...This review uses computed tomography (CT) with three-dimensional reconstructions to help describe some of the types and classifications of craniosyno …
Craniosynostosis is a complex condition, characterized by the premature fusion of one of more of the cranial sutures. ...This review …
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 cranios …
Craniosynostosis, in which 1 or more cranial sutures prematurely fuse, is associated with diverse environmental and genetic factors. …
Craniofacial syndromes.
Buchanan EP, Xue AS, Hollier LH Jr. Buchanan EP, et al. Plast Reconstr Surg. 2014 Jul;134(1):128e-153e. doi: 10.1097/PRS.0000000000000308. Plast Reconstr Surg. 2014. PMID: 25028828 Review.
Understand the most serious complications associated with each syndrome. 3. Formulate the best age-appropriate surgical plans. SUMMARY: Craniofacial syndromes fall into two major categories-those associated with craniosynostosis, and those associated with clefts. Ea …
Understand the most serious complications associated with each syndrome. 3. Formulate the best age-appropriate surgical plans. SUMMAR …
883 results