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

Year Number of Results
1982 1
1988 2
1989 2
1990 2
1991 2
1992 3
1993 1
1994 4
1995 1
1996 1
1997 1
1998 3
1999 2
2001 3
2002 6
2003 1
2005 4
2006 3
2007 2
2008 1
2009 5
2010 4
2011 3
2012 3
2013 4
2014 3
2015 1
2016 3
2017 2
2018 1
2019 1
2020 1
2021 3
2022 2
2023 1
2024 0

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78 results

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Page 1
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) rh …
The most common associated findings with rhombencephalosynapsis include hydrocephalus, mesencephalosynapsis, holoprosencephaly, ponto …
Teratogenesis of holoprosencephaly.
Cohen MM Jr, Shiota K. Cohen MM Jr, et al. Am J Med Genet. 2002 Apr 15;109(1):1-15. doi: 10.1002/ajmg.10258. Am J Med Genet. 2002. PMID: 11932986 Review.
Teratogenic causes of holoprosencephaly are critically assessed. A brief general review of holoprosencephaly is followed by four tables summarizing etiologic factors. Subjects evaluated here include: 1) maternal diabetes; 2) ethyl alcohol; 3) retinoic acid; 4
Teratogenic causes of holoprosencephaly are critically assessed. A brief general review of holoprosencephaly is followed by fo …
Four cholesterol-sensing proteins.
Lange Y, Steck TL. Lange Y, et al. Curr Opin Struct Biol. 1998 Aug;8(4):435-9. doi: 10.1016/s0959-440x(98)80119-x. Curr Opin Struct Biol. 1998. PMID: 9729733 Review.
What is the connection among the following three medical conditions: Niemann-Pick type C disease (a cause of mental retardation and early death), systemic lipidosis (in which an obscure side effect of numerous drugs transforms lysosomes into lamellar bodies), and holoprosencep
What is the connection among the following three medical conditions: Niemann-Pick type C disease (a cause of mental retardation and early de …
Monosomy 18p.
Turleau C. Turleau C. Orphanet J Rare Dis. 2008 Feb 19;3:4. doi: 10.1186/1750-1172-3-4. Orphanet J Rare Dis. 2008. PMID: 18284672 Free PMC article. Review.
A small subset of patients, about 10-15 percent of cases, present with severe brain/facial malformations evocative of holoprosencephaly spectrum disorders. In two-thirds of the cases, the 18p- syndrome is due to a mere terminal deletion occurring de novo, in one-third the …
A small subset of patients, about 10-15 percent of cases, present with severe brain/facial malformations evocative of holoprosencephaly
Developmental disorders of the dentition: an update.
Klein OD, Oberoi S, Huysseune A, Hovorakova M, Peterka M, Peterkova R. Klein OD, et al. Am J Med Genet C Semin Med Genet. 2013 Nov;163C(4):318-32. doi: 10.1002/ajmg.c.31382. Epub 2013 Oct 4. Am J Med Genet C Semin Med Genet. 2013. PMID: 24124058 Free PMC article. Review.
This is followed by a discussion of isolated as well as syndromic tooth agenesis, including Van der Woude syndrome (VWS), ectodermal dysplasias (EDs), oral-facial-digital (OFD) syndrome type I, Rieger syndrome, holoprosencephaly, and tooth anomalies associated with cleft l …
This is followed by a discussion of isolated as well as syndromic tooth agenesis, including Van der Woude syndrome (VWS), ectodermal dysplas …
The cavum septi pellucidi: why is it important?
Winter TC, Kennedy AM, Byrne J, Woodward PJ. Winter TC, et al. J Ultrasound Med. 2010 Mar;29(3):427-44. doi: 10.7863/jum.2010.29.3.427. J Ultrasound Med. 2010. PMID: 20194938 Review.
OBJECTIVE: The cavum septi pellucidi (CSP) is routinely imaged in the fetal brain during obstetric sonography; in fact, for well over a decade, assessment of the CSP has been considered part of the required elements of a standard examination of fetal morphology in guidelines deve …
OBJECTIVE: The cavum septi pellucidi (CSP) is routinely imaged in the fetal brain during obstetric sonography; in fact, for well over a deca …
Disorders of prosencephalic development.
Volpe P, Campobasso G, De Robertis V, Rembouskos G. Volpe P, et al. Prenat Diagn. 2009 Apr;29(4):340-54. doi: 10.1002/pd.2208. Prenat Diagn. 2009. PMID: 19184971 Review.
Abnormal ventral induction may result in disorders of formation, cleavage, and midline development of prosencephalic structures. Holoprosencephaly is a developmental field defect of impaired cleavage of prosencephalon. The most widely accepted classification of holopros
Abnormal ventral induction may result in disorders of formation, cleavage, and midline development of prosencephalic structures. Holopros
Holoprosencephaly and septo-optic dysplasia.
Fitz CR. Fitz CR. Neuroimaging Clin N Am. 1994 May;4(2):263-81. Neuroimaging Clin N Am. 1994. PMID: 8081628 Review.
Holoprosencephaly is a rare brain anomaly, which may be seen in liveborn neonates, although it is more common in stillbirths and abortions. ...Primary imaging findings include optic nerve hypoplasia and absent septum pellucidum. Septo-optic dysplasia somewhat resembles lob
Holoprosencephaly is a rare brain anomaly, which may be seen in liveborn neonates, although it is more common in stillbirths and abor
A Practical Approach to Supratentorial Brain Malformations: What Radiologists Should Know.
Yang E, Chu WCW, Lee EY. Yang E, et al. Radiol Clin North Am. 2017 Jul;55(4):609-627. doi: 10.1016/j.rcl.2017.02.005. Radiol Clin North Am. 2017. PMID: 28601171 Review.
It begins with a discussion of embryology and optimal imaging technique and then summarizes distinguishing imaging features for several major categories of cerebral malformation, including holoprosencephaly, gray matter heterotopia, lissencephaly/pachygyria, focal cortical …
It begins with a discussion of embryology and optimal imaging technique and then summarizes distinguishing imaging features for several majo …
Holoprosencephaly: genetic, neuroradiological, and clinical advances.
Hahn JS, Pinter JD. Hahn JS, et al. Semin Pediatr Neurol. 2002 Dec;9(4):309-19. doi: 10.1053/spen.2002.32507. Semin Pediatr Neurol. 2002. PMID: 12523555 Review.
Recent advances in genetics and neuroimaging have greatly contributed to our understanding of the spectrum of midline brain and craniofacial malformations known as holoprosencephaly. This review summarizes our current understanding of the epidemiology and molecular-genetic …
Recent advances in genetics and neuroimaging have greatly contributed to our understanding of the spectrum of midline brain and craniofacial …
78 results