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

Year Number of Results
1975 1
1984 1
1986 1
1989 1
1990 1
1991 2
1993 2
1994 1
1998 1
2000 1
2003 1
2005 1
2009 2
2011 2
2021 1
2022 2
2024 0

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20 results

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Page 1
Brain Organization and Human Diseases.
Sapir T, Sela-Donenfeld D, Karlinski M, Reiner O. Sapir T, et al. Cells. 2022 May 14;11(10):1642. doi: 10.3390/cells11101642. Cells. 2022. PMID: 35626679 Free PMC article. Review.
Prenatal diagnosis of middle interhemispheric variant of holoprosencephaly: review of literature and prenatal case series.
Tavano I, De Keersmaecker B, Aertsen M, De Catte L. Tavano I, et al. J Matern Fetal Neonatal Med. 2022 Dec;35(25):4976-4984. doi: 10.1080/14767058.2021.1873942. Epub 2021 Jan 17. J Matern Fetal Neonatal Med. 2022. PMID: 33455493 Review.
OBJECTIVE: Middle interhemispheric (MIH) variant of holoprosencephaly (HPE) or syntelencephaly is a rare prosencephalic cleavage disorder. ...A "PubMed" and "Trip database" search were conducted revealing six papers reporting on 11 prenatally diagnosed cases. RESULT …
OBJECTIVE: Middle interhemispheric (MIH) variant of holoprosencephaly (HPE) or syntelencephaly is a rare prosencephalic cleavage diso …
Holoprosencephaly: a guide to diagnosis and clinical management.
Raam MS, Solomon BD, Muenke M. Raam MS, et al. Indian Pediatr. 2011 Jun;48(6):457-66. doi: 10.1007/s13312-011-0078-x. Indian Pediatr. 2011. PMID: 21743112 Free PMC article. Review.
CONTEXT: Holoprosencephaly affects 1 in 8,000 live births and is the most common structural anomaly of the developing forebrain, resulting in facial dysmorphism, neurologic impairment, and additional clinical sequelae. ...EVIDENCE ACQUISITION: We used the PubMed database ( …
CONTEXT: Holoprosencephaly affects 1 in 8,000 live births and is the most common structural anomaly of the developing forebrain, resu …
Genetic forms of hypopituitarism and their manifestation in the neonatal period.
Alatzoglou KS, Dattani MT. Alatzoglou KS, et al. Early Hum Dev. 2009 Nov;85(11):705-12. doi: 10.1016/j.earlhumdev.2009.08.057. Epub 2009 Sep 16. Early Hum Dev. 2009. PMID: 19762173 Review.
The phenotype can be highly variable and may consist of isolated hypopituitarism, or more complex disorders such as septo-optic dysplasia (SOD) and holoprosencephaly. Neonates with congenital hypopituitarism may present with non-specific symptoms, with or without associate …
The phenotype can be highly variable and may consist of isolated hypopituitarism, or more complex disorders such as septo-optic dysplasia (S …
Central nervous system malformations in the CHARGE association.
Lin AE, Siebert JR, Graham JM Jr. Lin AE, et al. Am J Med Genet. 1990 Nov;37(3):304-10. doi: 10.1002/ajmg.1320370303. Am J Med Genet. 1990. PMID: 2260555 Review.
Twenty-six of 47 (55%) had definite central nervous system (CNS) malformations; arhinencephaly, with or without other defects (11), holoprosencephaly (2), holoprosencephaly with arhinencephaly (1), other forebrain defects (3), hindbrain defects (3), or other …
Twenty-six of 47 (55%) had definite central nervous system (CNS) malformations; arhinencephaly, with or without other defects (11), …
Prenatal diagnosis of triploidy associated with holoprosencephaly: a case report and review of the literature.
Bekdache GN, Begam M, Al Safi W, Mirghani H. Bekdache GN, et al. Am J Perinatol. 2009 Aug;26(7):479-83. doi: 10.1055/s-0029-1214248. Epub 2009 Apr 27. Am J Perinatol. 2009. PMID: 19399707 Review.
The latest search was done in June 2008. Literature review showed 11 reports with a total of 15 cases of holoprosencephaly associated with triploidy. ...Triploidy was mainly associated with the alobar type of holoprosencephaly. Only 3 (20%) cases had associat …
The latest search was done in June 2008. Literature review showed 11 reports with a total of 15 cases of holoprosencephaly ass …
Holoprosencephaly: a defect in brain patterning.
Golden JA. Golden JA. J Neuropathol Exp Neurol. 1998 Nov;57(11):991-9. doi: 10.1097/00005072-199811000-00001. J Neuropathol Exp Neurol. 1998. PMID: 9825935 Review. No abstract available.
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.
OBJECTIVE: To examine the performance of the 11-13 weeks scan in detecting non-chromosomal abnormalities. METHODS: Prospective first-trimester screening study for aneuploidies, including basic examination of the fetal anatomy, in 45 191 pregnancies. ...Fetal abnormalities …
OBJECTIVE: To examine the performance of the 11-13 weeks scan in detecting non-chromosomal abnormalities. METHODS: Prospective first- …
Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly.
Palacios J, Gamallo C, García M, Rodríguez JI. Palacios J, et al. Am J Med Genet. 1993 Jul 1;46(6):641-6. doi: 10.1002/ajmg.1320460608. Am J Med Genet. 1993. PMID: 8362905 Review.
In the present study, the quantitation of thyrocalcitonin immunoreactive cells (C-cells) has been used to evaluate whether cells derived from the cranial neural crest are or are not present in normal proportions in patients with this anomaly. Thyroid sections from 11 such …
In the present study, the quantitation of thyrocalcitonin immunoreactive cells (C-cells) has been used to evaluate whether cells derived fro …
Median facial malformations and their implications for brain malformations.
DeMyer W. DeMyer W. Birth Defects Orig Artic Ser. 1975;11(7):155-81. Birth Defects Orig Artic Ser. 1975. PMID: 764897 Review.
When combined in typical patterns with other median plane facial defects, the patient almost certainly has holoprosencephaly, and has a poor prognosis for useful psychomotor development and survival. ...
When combined in typical patterns with other median plane facial defects, the patient almost certainly has holoprosencephaly, and has …
20 results