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

Year Number of Results
1975 1
1976 2
1979 1
1982 2
1984 1
1985 1
1986 3
1988 5
1989 8
1990 7
1991 9
1992 6
1993 10
1994 6
1995 5
1996 3
1997 6
1998 15
1999 10
2000 18
2001 20
2002 12
2003 13
2004 4
2005 11
2006 9
2007 12
2008 7
2009 14
2010 30
2011 16
2012 12
2013 7
2014 12
2015 11
2016 16
2017 7
2018 15
2019 10
2020 12
2021 9
2022 10
2023 2

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368 results

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Page 1
First-trimester fetal neurosonography: technique and diagnostic potential.
Volpe N, Dall'Asta A, Di Pasquo E, Frusca T, Ghi T. Volpe N, et al. Ultrasound Obstet Gynecol. 2021 Feb;57(2):204-214. doi: 10.1002/uog.23149. Ultrasound Obstet Gynecol. 2021. PMID: 33049801 Free article. Review.
Using this basic approach, almost all cases of acrania, alobar holoprosencephaly and cephalocele are detected. However, the majority of other fetal brain abnormalities remain undiagnosed until the midtrimester. ...
Using this basic approach, almost all cases of acrania, alobar holoprosencephaly and cephalocele are detected. However, the majority …
Holoprosencephaly.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B13-B16. doi: 10.1016/j.ajog.2020.08.178. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168217 Review. No abstract available.
First and second trimester screening for fetal structural anomalies.
Edwards L, Hui L. Edwards L, et al. Semin Fetal Neonatal Med. 2018 Apr;23(2):102-111. doi: 10.1016/j.siny.2017.11.005. Epub 2017 Dec 9. Semin Fetal Neonatal Med. 2018. PMID: 29233624 Review.
Approximately one-half of all major structural anomalies can now be detected in the first trimester, including acrania/anencephaly, abdominal wall defects, holoprosencephaly and cystic hygromata. Due to the ongoing development of some organ systems however, some anomalies …
Approximately one-half of all major structural anomalies can now be detected in the first trimester, including acrania/anencephaly, abdomina …
Neuropathology of holoprosencephaly.
Fallet-Bianco C. Fallet-Bianco C. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):214-228. doi: 10.1002/ajmg.c.31623. Am J Med Genet C Semin Med Genet. 2018. PMID: 30182440 Review.
Holoprosencephaly (HPE) is a primary disorder of neural induction and patterning of the rostral neural tube resulting in noncleavage of the forebrain with failure to form two separate distinct hemispheres. ...
Holoprosencephaly (HPE) is a primary disorder of neural induction and patterning of the rostral neural tube resulting in noncleavage …
ZIC2 in Holoprosencephaly.
Barratt KS, Arkell RM. Barratt KS, et al. Adv Exp Med Biol. 2018;1046:269-299. doi: 10.1007/978-981-10-7311-3_14. Adv Exp Med Biol. 2018. PMID: 29442327 Review.
The ZIC2 transcription factor is one of the most commonly mutated genes in Holoprosencephaly (HPE) probands. HPE is a severe congenital defect of forebrain development which occurs when the cerebral hemispheres fail to separate during the early stages of organogenesis and …
The ZIC2 transcription factor is one of the most commonly mutated genes in Holoprosencephaly (HPE) probands. HPE is a severe congenit …
Prenatal diagnosis of holoprosencephaly.
Kousa YA, du Plessis AJ, Vezina G. Kousa YA, et al. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):206-213. doi: 10.1002/ajmg.c.31618. Epub 2018 May 17. Am J Med Genet C Semin Med Genet. 2018. PMID: 29770996 Review.
Holoprosencephaly is a spectrum of congenital defects of forebrain development characterized by incomplete separation of the cerebral hemispheres. ...Using an advanced MRI protocol and a 1.5-Tesla magnet, we show radiographic data diagnostic for the holoprosencephaly …
Holoprosencephaly is a spectrum of congenital defects of forebrain development characterized by incomplete separation of the cerebral …
Rhomboencephalosynapsis: Review of the Literature.
Fouda MA, Kim TY, Cohen AR. Fouda MA, et al. World Neurosurg. 2022 Mar;159:48-53. doi: 10.1016/j.wneu.2021.12.062. Epub 2021 Dec 22. World Neurosurg. 2022. PMID: 34954057 Review.
The most common associated findings with rhombencephalosynapsis include hydrocephalus, mesencephalosynapsis, holoprosencephaly, pontocerebellar hypoplasia, corpus callosum dysgenesis, and absence of septum pellucidum. Patients can be categorized into 4 groups: 1) rhombence …
The most common associated findings with rhombencephalosynapsis include hydrocephalus, mesencephalosynapsis, holoprosencephaly, ponto …
Holoprosencephaly in the genomics era.
Roessler E, Hu P, Muenke M. Roessler E, et al. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):165-174. doi: 10.1002/ajmg.c.31615. Epub 2018 May 17. Am J Med Genet C Semin Med Genet. 2018. PMID: 29770992 Review.
Holoprosencephaly (HPE) is the direct consequence of specific genetic and/or environmental insults interrupting the midline specification of the nascent forebrain. ...
Holoprosencephaly (HPE) is the direct consequence of specific genetic and/or environmental insults interrupting the midline specifica …
Neuro-osteology.
Kjaer I. Kjaer I. Crit Rev Oral Biol Med. 1998;9(2):224-44. doi: 10.1177/10454411980090020501. Crit Rev Oral Biol Med. 1998. PMID: 9603237 Review.
Results from pre-natal investigations provide information on the post-natal diagnosis of children with congenital developmental disorders in the central nervous system. Examples of these are myelomeningocele and holoprosencephaly. Three steps are important in clinical neur …
Results from pre-natal investigations provide information on the post-natal diagnosis of children with congenital developmental disorders in …
368 results