Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1998 1
2001 1
2002 1
2004 1
2007 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

5 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Holoprosencephaly caudal dysgenesis"
Page 1
Holoprosencephaly--topologic variations in a liveborn series: a general model based upon MRI analysis.
Takahashi TS, Kinsman S, Makris N, Grant E, Haselgrove C, McInerney S, Kennedy DN, Takahashi TA, Fredrickson K, Mori S, Caviness VS. Takahashi TS, et al. J Neurocytol. 2004 Jan;33(1):23-35. doi: 10.1023/B:NEUR.0000029646.75645.9c. J Neurocytol. 2004. PMID: 15173630
We present an MRI-based anatomic analysis of a series of 9 human brains, representing lobar, semilobar and alobar forms of holoprosencephaly. The analysis of these variable forms of the malformation is based upon a topologic systematics established in a prior analysis of a …
We present an MRI-based anatomic analysis of a series of 9 human brains, representing lobar, semilobar and alobar forms of holoprosenceph …
Midline skeletodental morphology in holoprosencephaly.
Kjaer I, Keeling JW, Fischer Hansen B, Becktor KB. Kjaer I, et al. Cleft Palate Craniofac J. 2002 May;39(3):357-63. doi: 10.1597/1545-1569_2002_039_0357_msmih_2.0.co_2. Cleft Palate Craniofac J. 2002. PMID: 12019014
OBJECTIVE: The purpose of the present study was to analyze histologically the midline structures in a human fetus with holoprosencephaly and a single median maxillary central incisor. METHODS: A human male fetus, CRL 137 mm, postconceptional age 18 weeks, with a diagnosis …
OBJECTIVE: The purpose of the present study was to analyze histologically the midline structures in a human fetus with holoprosencephaly …
Expression of Sonic Hedgehog downstream genes is modified in rat embryos exposed in utero to a distal inhibitor of cholesterol biosynthesis.
Gofflot F, Gaoua W, Bourguignon L, Roux C, Picard JJ. Gofflot F, et al. Dev Dyn. 2001 Feb;220(2):99-111. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1092>3.0.CO;2-G. Dev Dyn. 2001. PMID: 11169843 Free article.
Holoprosencephaly is a common developmental anomaly of the forebrain and midface, that has been associated with mutations in the Sonic Hedgehog gene, and with perturbations of cholesterol synthesis and metabolism in mammalian embryos. ...Later in development this reduction …
Holoprosencephaly is a common developmental anomaly of the forebrain and midface, that has been associated with mutations in the Soni …
Cyclopia, aprosencephaly, and acardiac twinning: Is hypoxia-ischemia a unifying mechanism?
Siebert JR. Siebert JR. Am J Med Genet A. 2007 Dec 15;143A(24):3100-6. doi: 10.1002/ajmg.a.32027. Am J Med Genet A. 2007. PMID: 18000898
As a result, cranial tissues are less likely to be perfused with oxygenated blood than caudal tissues. A host of craniocerebral anomalies are observed in acardia, including total absence of the head and brain, rudimentary brain, anencephaly, holoprosencephaly, neuro …
As a result, cranial tissues are less likely to be perfused with oxygenated blood than caudal tissues. A host of craniocerebral anoma …
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. III: primary field defects, sequences, and other complex anomalies.
Oostra RJ, Baljet B, Verbeeten BW, Hennekam RC. Oostra RJ, et al. Am J Med Genet. 1998 Oct 30;80(1):46-59. doi: 10.1002/(sici)1096-8628(19981102)80:1<46::aid-ajmg8>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9800911
The Museum Vrolik collection of the Department of Anatomy and Embryology of the Academic Medical Center, University of Amsterdam, founded by Gerardus Vrolik (1775-1859) and his son Willem Vrolik (1801-1863), consists of more than 5,000 specimens of human and animal anatomy, embry …
The Museum Vrolik collection of the Department of Anatomy and Embryology of the Academic Medical Center, University of Amsterdam, founded by …