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

Year Number of Results
1981 1
1986 1
1987 1
1989 1
1990 1
1991 3
1993 2
1997 4
1998 1
1999 1
2000 5
2001 2
2003 2
2004 1
2005 4
2006 2
2007 2
2008 2
2009 1
2010 3
2011 5
2012 3
2013 3
2014 4
2015 1
2016 2
2017 4
2018 2
2019 3
2020 2
2021 2
2022 2
2023 2
2024 1

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71 results

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Page 1
Congenital facial palsy and emotion processing: The case of Moebius syndrome.
De Stefani E, Nicolini Y, Belluardo M, Ferrari PF. De Stefani E, et al. Genes Brain Behav. 2019 Jan;18(1):e12548. doi: 10.1111/gbb.12548. Genes Brain Behav. 2019. PMID: 30604920 Free article. Review.
Embodied cognition theories suggest that we understand others' emotions by reproducing the perceived expression in our own facial musculature (facial mimicry) and the mere observation of a facial expression can evoke the corresponding emotion in the perceiver …
Embodied cognition theories suggest that we understand others' emotions by reproducing the perceived expression in our own facial mus …
Management of Bilateral Facial Palsy.
Domeshek LF, Zuker RM, Borschel GH. Domeshek LF, et al. Otolaryngol Clin North Am. 2018 Dec;51(6):1213-1226. doi: 10.1016/j.otc.2018.07.014. Epub 2018 Aug 27. Otolaryngol Clin North Am. 2018. PMID: 30166122 Review.
Bilateral facial paralysis is a rare entity that occurs in both pediatric and adult patients and can have congenital or acquired causes. When paralysis does not resolve with conservative or medical management, surgical intervention may be indicated. This article pre …
Bilateral facial paralysis is a rare entity that occurs in both pediatric and adult patients and can have congenital or acquir …
The congenital cranial dysinnervation disorders.
Gutowski NJ, Chilton JK. Gutowski NJ, et al. Arch Dis Child. 2015 Jul;100(7):678-81. doi: 10.1136/archdischild-2014-307035. Epub 2015 Jan 29. Arch Dis Child. 2015. PMID: 25633065 Review.
Congenital cranial dysinnervation disorders (CCDD) encompass a number of related conditions and includes Duane syndrome, congenital fibrosis of the external ocular muscles, Mobius syndrome, congenital ptosis and hereditary congenital …
Congenital cranial dysinnervation disorders (CCDD) encompass a number of related conditions and includes Duane syndrome, co …
Congenital cranial dysinnervation disorders.
Singh A, Pandey PK, Agrawal A, Mittal SK, Rana KM, Bahuguna C. Singh A, et al. Int Ophthalmol. 2017 Dec;37(6):1369-1381. doi: 10.1007/s10792-016-0388-z. Epub 2016 Nov 11. Int Ophthalmol. 2017. PMID: 27837354 Review.
The European Neuromuscular Centre (ENMC) derived the term Congenital Cranial Dysinnervation Disorders in 2002 at an international workshop for a group of congenital neuromuscular diseases. CCDDs are congenital, non-progressive ophthalmoplegia with restriction …
The European Neuromuscular Centre (ENMC) derived the term Congenital Cranial Dysinnervation Disorders in 2002 at an international wor …
Prenatal exposure to misoprostol and congenital anomalies: systematic review and meta-analysis.
da Silva Dal Pizzol T, Knop FP, Mengue SS. da Silva Dal Pizzol T, et al. Reprod Toxicol. 2006 Nov;22(4):666-71. doi: 10.1016/j.reprotox.2006.03.015. Epub 2006 Jun 5. Reprod Toxicol. 2006. PMID: 16750609 Review.
None of the studies analyzed other adverse effects from misoprostol on the outcome from gestation. Increased risks of congenital anomalies related to misoprostol use were found for any congenital defect (OR=3.56; 95% CI: 0.98-12.98), Mobius sequence (OR=25.31 …
None of the studies analyzed other adverse effects from misoprostol on the outcome from gestation. Increased risks of congenital anom …
Congenital and infantile myotonic dystrophy.
Echenne B, Bassez G. Echenne B, et al. Handb Clin Neurol. 2013;113:1387-93. doi: 10.1016/B978-0-444-59565-2.00009-5. Handb Clin Neurol. 2013. PMID: 23622362 Review.
As consequence of the non coding unstable CTG repeat expansion mutation, DM1 presents as an extremely wide and diverse clinical continuum ranging from antenatal to late adult forms, the complexity of the disease being reinforced by multisystemic involvement. The congenital …
As consequence of the non coding unstable CTG repeat expansion mutation, DM1 presents as an extremely wide and diverse clinical continuum ra …
Imaging of congenital cranial dysinnervation disorders: What radiologist wants to know?
Razek AAKA, Maher H, Kasem MA, Helmy E. Razek AAKA, et al. Clin Imaging. 2021 Mar;71:106-116. doi: 10.1016/j.clinimag.2020.10.055. Epub 2020 Nov 6. Clin Imaging. 2021. PMID: 33189029 Review.
Duane retraction syndrome shows absent or hypoplasic 6th cranial nerve and preserved extraocular muscles (EOM). Mobius syndrome shows absent 7th and 6th cranial nerves, absence of facial colliculus, flattening of the dorsal aspect of the pons, hypoplas …
Duane retraction syndrome shows absent or hypoplasic 6th cranial nerve and preserved extraocular muscles (EOM). Mobius synd …
Developmental facial paralysis: a review.
Terzis JK, Anesti K. Terzis JK, et al. J Plast Reconstr Aesthet Surg. 2011 Oct;64(10):1318-33. doi: 10.1016/j.bjps.2011.04.015. Epub 2011 Jul 2. J Plast Reconstr Aesthet Surg. 2011. PMID: 21724478 Review.
The purpose of this study is to clarify the confusing nomenclature and pathogenesis of Developmental Facial Paralysis, and how it can be differentiated from other causes of facial paralysis present at birth. ...The 30 years experience of our center in the management …
The purpose of this study is to clarify the confusing nomenclature and pathogenesis of Developmental Facial Paralysis, and how it can …
Branchial arch syndromes.
Alfi D, Lam D, Gateno J. Alfi D, et al. Atlas Oral Maxillofac Surg Clin North Am. 2014 Sep;22(2):167-73. doi: 10.1016/j.cxom.2014.04.003. Epub 2014 Jul 15. Atlas Oral Maxillofac Surg Clin North Am. 2014. PMID: 25171997 Review. No abstract available.
Divergent roles of Plexin D1 in cancer.
Vivekanadhan S, Mukhopadhyay D. Vivekanadhan S, et al. Biochim Biophys Acta Rev Cancer. 2019 Aug;1872(1):103-110. doi: 10.1016/j.bbcan.2019.05.004. Epub 2019 May 30. Biochim Biophys Acta Rev Cancer. 2019. PMID: 31152824 Free PMC article. Review.
Mutations in Plexin D1 have been implicated in pathologic conditions such as truncus arteriosus and Mobius syndrome. Emerging data show that expression of Plexin D1 is deregulated in several cancers; it can support tumor development by aiding in tumor metastasis and …
Mutations in Plexin D1 have been implicated in pathologic conditions such as truncus arteriosus and Mobius syndrome. Emerging …
71 results