Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1991
2025

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

Year Number of Results
1991 2
1996 1
1997 1
1998 1
2001 1
2011 5
2012 2
2013 1
2022 1
2024 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

15 results

Results by year

Filters applied: . Clear all
Page 1
The spectrum of median craniofacial dysplasia.
Allam KA, Wan DC, Kawamoto HK, Bradley JP, Sedano HO, Saied S. Allam KA, et al. Plast Reconstr Surg. 2011 Feb;127(2):812-821. doi: 10.1097/PRS.0b013e318200aa08. Plast Reconstr Surg. 2011. PMID: 21285785 Review.
Given the multiple permutations in craniofacial malformations, classification of median craniofacial dysplasia or midline Tessier no. 0 to 14 clefts has been difficult and disjointed. In this review, the authors present a summary of normal embryology, prior terminology, an …
Given the multiple permutations in craniofacial malformations, classification of median craniofacial dysplasia or midline Tessier no. 0 to …
Patterning of the antero-ventral mammalian brain: Lessons from holoprosencephaly comparative biology in man and mouse.
Barratt KS, Drover KA, Thomas ZM, Arkell RM. Barratt KS, et al. WIREs Mech Dis. 2022 Jul;14(4):e1552. doi: 10.1002/wsbm.1552. Epub 2022 Feb 8. WIREs Mech Dis. 2022. PMID: 35137563 Review.
Comparative biology has extended the holoprosencephaly network via the inclusion of gene mutations from multiple signaling pathways known to be required for anterior midline formation. ...The challenges now at the forefront of holoprosencephaly research include deci …
Comparative biology has extended the holoprosencephaly network via the inclusion of gene mutations from multiple signaling pathways k …
Congenital nasal pyriform aperture stenosis: a report of 10 cases and literature review.
Visvanathan V, Wynne DM. Visvanathan V, et al. Int J Pediatr Otorhinolaryngol. 2012 Jan;76(1):28-30. doi: 10.1016/j.ijporl.2011.09.016. Epub 2011 Oct 22. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22024577 Review.
Surgical widening of the pyriform aperture was performed at an average of 14 days at birth. Associated malformations include holoprosencephaly, hypopituitarism, cardiac and urogenital malformations. ...
Surgical widening of the pyriform aperture was performed at an average of 14 days at birth. Associated malformations include holop
Molecular genetics of human microcephaly.
Mochida GH, Walsh CA. Mochida GH, et al. Curr Opin Neurol. 2001 Apr;14(2):151-6. doi: 10.1097/00019052-200104000-00003. Curr Opin Neurol. 2001. PMID: 11262728 Review.
Solitary median maxillary central incisor syndrome (SMMCI) with congenital nasal puriform aperture stenosis: literature review and case report with comprehensive dental treatment and 14 years follow-up.
Lygidakis NN, Chatzidimitriou K, Petrou N, Lygidakis NA. Lygidakis NN, et al. Eur Arch Paediatr Dent. 2013 Dec;14(6):417-23. doi: 10.1007/s40368-013-0044-5. Epub 2013 Jun 18. Eur Arch Paediatr Dent. 2013. PMID: 23775592 Review.
In more severe cases, SMMCI has been associated with holoprosencephaly, the CHARGE and the VACTERL association. Also, published sporadic cases have been related with rare variants of ectodermal dysplasia, chromosomal abnormalities, precocious puberty, hypothalamic hamartom …
In more severe cases, SMMCI has been associated with holoprosencephaly, the CHARGE and the VACTERL association. Also, published spora …
Prenatal neurologic anomalies: sonographic diagnosis and treatment.
De Catte L, De Keersmaeker B, Claus F. De Catte L, et al. Paediatr Drugs. 2012 Jun 1;14(3):143-55. doi: 10.2165/11597030-000000000-00000. Paediatr Drugs. 2012. PMID: 22242843 Review.
The failure of prosencephalic midline induction and development results in midline defects ranging from alobar holoprosencephaly to isolated corpus callosum defects. The detection of callosal abnormaties is enhanced by 3D ultrasound, but counseling on neurodevelopmental ou …
The failure of prosencephalic midline induction and development results in midline defects ranging from alobar holoprosencephaly to i …
Challenges in the diagnosis of fetal non-chromosomal abnormalities at 11-13 weeks.
Syngelaki A, Chelemen T, Dagklis T, Allan L, Nicolaides KH. Syngelaki A, et al. Prenat Diagn. 2011 Jan;31(1):90-102. doi: 10.1002/pd.2642. Prenat Diagn. 2011. PMID: 21210483 Review.
The early scan detected all cases of acrania, alobar holoprosencephaly, exomphalos, gastroschisis, megacystis and body stalk anomaly, 77% of absent hand or foot, 50% of diaphragmatic hernia, 50% of lethal skeletal dysplasias, 60% of polydactyly, 34% of major cardiac defect …
The early scan detected all cases of acrania, alobar holoprosencephaly, exomphalos, gastroschisis, megacystis and body stalk anomaly, …
Prenatal detection of distal 18p deletion by chromosomal microarray analysis: Three case reports and literature review.
Xu T, Yue F, He J, Zhang H, Liu R. Xu T, et al. Medicine (Baltimore). 2024 Jul 26;103(30):e39046. doi: 10.1097/MD.0000000000039046. Medicine (Baltimore). 2024. PMID: 39058883 Free PMC article. Review.
Meanwhile, CMA detected 4.37 Mb (case 1), 7.26 Mb (case 2) and 14.97 Mb (case 3) deletions in chromosome 18p region. All 3 pregnancies were terminated finally according to genetic counseling based upon abnormal CMA results. ...Increased nuchal translucency and holoprose
Meanwhile, CMA detected 4.37 Mb (case 1), 7.26 Mb (case 2) and 14.97 Mb (case 3) deletions in chromosome 18p region. All 3 pregnancie …
An acardiac twin with advanced brain development and a minor form of holoprosencephaly and intracerebral retina-like pigmented tissue: a case report and review of the literature.
Huss S, Fronhoffs F, Gembruch U, Loeffler K, Born M, Gessi M, Kuchelmeister K, Müller AM. Huss S, et al. Pediatr Dev Pathol. 2011 Sep-Oct;14(5):411-7. doi: 10.2350/10-09-0916-CR.1. Epub 2011 Apr 13. Pediatr Dev Pathol. 2011. PMID: 21488711 Review.
We report, according to our review of the literature, for the first time, a very unusual case of acardius with features of acardius amorphus and acormus (fused head and malformed axial skeleton without macroscopically detectable internal organs) with lobar holoprosencephaly
We report, according to our review of the literature, for the first time, a very unusual case of acardius with features of acardius amorphus …
Holoprosencephaly and chromosomal anomalies.
Chow BH, Loh SF, Yan YL, Ang HK, Yeo GS. Chow BH, et al. Singapore Med J. 1996 Aug;37(4):394-7. Singapore Med J. 1996. PMID: 8993141 Review.
Holoprosencephaly is a rare cerebral malformation resulting from failure or incomplete cleavage of the forebrain. ...Chromosomal anomalies, diabetes mellitus, alcohol, autosomal recessive inheritance and toxins have been implicated. We describe seven cases of holoprosen
Holoprosencephaly is a rare cerebral malformation resulting from failure or incomplete cleavage of the forebrain. ...Chromosomal anom
15 results