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

Year Number of Results
1990 1
1991 1
1996 1
2000 2
2001 2
2003 1
2004 1
2005 1
2008 2
2012 1
2013 1
2015 1
2016 2
2017 2
2018 1
2019 1
2021 2
2024 0

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19 results

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Page 1
Imaging Spectrum of Calvarial Abnormalities.
Khodarahmi I, Alizai H, Chalian M, Alaia EF, Burke CJ, Slasky SE, Wenokor C. Khodarahmi I, et al. Radiographics. 2021 Jul-Aug;41(4):1144-1163. doi: 10.1148/rg.2021200198. Radiographics. 2021. PMID: 34197249 Review.
Prior trauma (congenital depression, leptomeningeal cysts, posttraumatic osteolysis), surgical intervention (flap osteonecrosis and burr holes), infection, and inflammatory processes (sarcoidosis) can result in focal bone loss, which may also be seen with idiopathic disorders wit …
Prior trauma (congenital depression, leptomeningeal cysts, posttraumatic osteolysis), surgical intervention (flap osteonecrosis and burr hol …
Syndromes, disorders and maternal risk factors associated with neural tube defects (VII).
Chen CP. Chen CP. Taiwan J Obstet Gynecol. 2008 Sep;47(3):276-82. doi: 10.1016/S1028-4559(08)60124-2. Taiwan J Obstet Gynecol. 2008. PMID: 18935989 Free article. Review.
This article provides a comprehensive review of the syndromes, disorders and maternal risk factors associated with NTDs, including DK phocomelia syndrome (von Voss-Cherstvoy syndrome), Siegel-Bartlet syndrome, fetal warfarin syndrome, craniotelencephalic dysplasia, Czeizel-Losonc …
This article provides a comprehensive review of the syndromes, disorders and maternal risk factors associated with NTDs, including DK phocom …
Craniosynostosis and related limb anomalies.
Wilkie AO, Oldridge M, Tang Z, Maxson RE Jr. Wilkie AO, et al. Novartis Found Symp. 2001;232:122-33; discussion 133-43. doi: 10.1002/0470846658.ch9. Novartis Found Symp. 2001. PMID: 11277076 Review.
We have recently identified three MSX2 mutations associated with a different cranial phenotype, parietal foramina. DNA binding studies show that the craniosynostosis and parietal foramina arise from gain and loss of function, respectively....
We have recently identified three MSX2 mutations associated with a different cranial phenotype, parietal foramina. DNA binding …
Hereditary cranium bifidum and symmetric parietal foramina are the same entity.
Little BB, Knoll KA, Klein VR, Heller KB. Little BB, et al. Am J Med Genet. 1990 Apr;35(4):453-8. doi: 10.1002/ajmg.1320350402. Am J Med Genet. 1990. PMID: 2185629 Review.
McKusick's catalog contains only one family with cranium bifidum but several familial reports of symmetrical parietal foramina. Available information indicates that cranium bifidum and symmetrical parietal foramina are inherited in an autosomal dominan …
McKusick's catalog contains only one family with cranium bifidum but several familial reports of symmetrical parietal foramina …
[Cranium bifidum occultum].
Kimura Y, Moritake K. Kimura Y, et al. Ryoikibetsu Shokogun Shirizu. 2000;(28 Pt 3):374. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11043269 Review. Japanese. No abstract available.
Enlarged parietal foramina: a review of genetics, prognosis, radiology, and treatment.
Griessenauer CJ, Veith P, Mortazavi MM, Stewart C, Grochowsky A, Loukas M, Tubbs RS. Griessenauer CJ, et al. Childs Nerv Syst. 2013 Apr;29(4):543-7. doi: 10.1007/s00381-012-1982-7. Epub 2012 Dec 4. Childs Nerv Syst. 2013. PMID: 23207976 Review.
In contrast to the normal small parietal foramina, enlarged parietal foramina are a hereditary condition and genes associated with it have been identified. ...This article provides a comprehensive review of the current knowledge of enlarged parietal …
In contrast to the normal small parietal foramina, enlarged parietal foramina are a hereditary condition and gen …
Foramina parietalia permagna: familial and radiological evaluation of two cases and review of literature.
Gabor L, Canaz H, Canaz G, Kara N, Gulec EY, Alatas I. Gabor L, et al. Childs Nerv Syst. 2017 May;33(5):853-857. doi: 10.1007/s00381-016-3315-8. Epub 2016 Dec 14. Childs Nerv Syst. 2017. PMID: 27975139 Review.
Foramina parietalia permagna have an autosomal dominant inheritance, and it is showed that mutations in chromosome 5 and 11 are causing this anomaly. Enlarged parietal foramina occurs extremely rare. They are usually asymptomatic, but occasional headache, vomiting, …
Foramina parietalia permagna have an autosomal dominant inheritance, and it is showed that mutations in chromosome 5 and 11 are causing this …
Common surgical pitfalls in the skull.
Keskil S, Gözil R, Calgüner E. Keskil S, et al. Surg Neurol. 2003 Mar;59(3):228-31; discussion 231. doi: 10.1016/s0090-3019(02)01038-8. Surg Neurol. 2003. PMID: 12681561 Review.
METHODS: A surgical reminder of possible pitfalls was composed based on the incidences of most of the minor variations such as the supraorbital notch, frontal foramen, metopism, foramen caecum, parietal foramina, bony defects in the fossa occipitalis cerebellaris, I …
METHODS: A surgical reminder of possible pitfalls was composed based on the incidences of most of the minor variations such as the supraorbi …
Craniofacial anomalies: from development to molecular pathogenesis.
Rice DP. Rice DP. Curr Mol Med. 2005 Nov;5(7):699-722. doi: 10.2174/156652405774641043. Curr Mol Med. 2005. PMID: 16305494 Review.
The more common craniofacial anomalies cleft lip and palate and craniosynostosis, as well as cleidocranial dysplasia, hemifacial microsomia, holoprosencephaly, enlarged parietal foramina, Treacher Collins syndrome and cherubism are discussed....
The more common craniofacial anomalies cleft lip and palate and craniosynostosis, as well as cleidocranial dysplasia, hemifacial microsomia, …
19 results