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

Year Number of Results
1988 1
1989 1
1992 1
1994 3
1996 2
1997 1
1998 2
1999 4
2000 4
2001 3
2002 2
2003 4
2005 4
2006 1
2007 1
2008 3
2009 6
2010 5
2011 1
2012 1
2014 3
2015 2
2016 3
2017 1
2018 5
2019 4
2020 5
2021 2
2022 4
2023 3
2024 0

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72 results

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Page 1
Delineating septo-optic dysplasia.
Lubinsky M, Encha-Razavi F. Lubinsky M, et al. Birth Defects Res. 2022 Dec 1;114(20):1343-1353. doi: 10.1002/bdr2.2095. Epub 2022 Oct 6. Birth Defects Res. 2022. PMID: 36200678 Review.
ONH disruptions can spread to pituitary, SPD disruptions to the cerebral cortex, causing schizencephaly and related anomalies. Pituitary defects are rare without ONH, and cortical findings are rare without SPD. ...
ONH disruptions can spread to pituitary, SPD disruptions to the cerebral cortex, causing schizencephaly and related anomalies. Pituit …
Neuronal Migration Disorders.
Roberts B. Roberts B. Radiol Technol. 2018 Jan;89(3):279-295. Radiol Technol. 2018. PMID: 29298944 Review.
Magnetic resonance imaging plays a primary role in the diagnosis and classification of neuronal migration disorders. These disorders include polymicrogyria, schizencephaly, lissencephaly, heterotopia, and focal cortical dysplasia. ...
Magnetic resonance imaging plays a primary role in the diagnosis and classification of neuronal migration disorders. These disorders include …
Intracranial arachnoid cysts.
Ahmed AK, Cohen AR. Ahmed AK, et al. Childs Nerv Syst. 2023 Oct;39(10):2771-2778. doi: 10.1007/s00381-023-06066-0. Epub 2023 Jul 19. Childs Nerv Syst. 2023. PMID: 37466684 Review.
The underlying etiology is not entirely known, and they occur in greater proportion in males and in greater incidence with various genetic conditions including Down syndrome, mucopolysaccharidosis, schizencephaly, neurofibromatosis, autosomal dominant polycystic kidney dis …
The underlying etiology is not entirely known, and they occur in greater proportion in males and in greater incidence with various genetic c …
Imaging of Congenital Malformations of the Brain.
Fenton LZ. Fenton LZ. Clin Perinatol. 2022 Sep;49(3):587-601. doi: 10.1016/j.clp.2022.05.002. Epub 2022 Aug 22. Clin Perinatol. 2022. PMID: 36113924 Review.
The third and longest timeframe include the disorders of neuronal migration and proliferation (gestational weeks eight-25) and include malformations of cortical development: lissencephaly, polymicrogyria, schizencephaly, gray matter heterotopia, and corpus callosal dysgene …
The third and longest timeframe include the disorders of neuronal migration and proliferation (gestational weeks eight-25) and include malfo …
Prenatal stroke.
Govaert P. Govaert P. Semin Fetal Neonatal Med. 2009 Oct;14(5):250-66. doi: 10.1016/j.siny.2009.07.008. Epub 2009 Aug 6. Semin Fetal Neonatal Med. 2009. PMID: 19664975 Review.
Forebrain lesions of arterial type present as porencephaly, (hemi)hydranencephaly, multicystic encephalopathy or schizencephaly. Venous prenatal forebrain stroke presents as simple porencephaly (in some of genetic nature) and sinus thrombosis. ...
Forebrain lesions of arterial type present as porencephaly, (hemi)hydranencephaly, multicystic encephalopathy or schizencephaly. Veno …
Schizencephaly: A Review of 734 Patients.
Braga VL, da Costa MDS, Riera R, Dos Santos Rocha LP, de Oliveira Santos BF, Matsumura Hondo TT, de Oliveira Chagas M, Cavalheiro S. Braga VL, et al. Pediatr Neurol. 2018 Oct;87:23-29. doi: 10.1016/j.pediatrneurol.2018.08.001. Epub 2018 Aug 8. Pediatr Neurol. 2018. PMID: 30501885 Review.
BACKGROUND: Schizencephaly is a rare congenital cerebral malformation associated with serious neurological manifestations. The number of studies regarding schizencephaly is limited. METHODS: We conducted a literature review and extracted data from the case reports. …
BACKGROUND: Schizencephaly is a rare congenital cerebral malformation associated with serious neurological manifestations. The number …
Schizencephaly and the Neurodevelopmental Model of Psychosis.
Patwal R, Pai NM, Ganjekar S, Arshad F, Alladi S, Sharma MK, Desai G, Chaturvedi SK. Patwal R, et al. Neurol India. 2022 Mar-Apr;70(2):740-743. doi: 10.4103/0028-3886.344662. Neurol India. 2022. PMID: 35532651 Free article. Review.
BACKGROUND: Schizencephaly is a rare congenital disorder of cerebral cortical development. ...RESULTS: MRI findings are suggestive of closed lip schizencephaly. CONCLUSION: This case helps us in understanding the neurodevelopmental model and functional neuroanatomy …
BACKGROUND: Schizencephaly is a rare congenital disorder of cerebral cortical development. ...RESULTS: MRI findings are suggestive of …
A journey through formation and malformations of the neo-cortex.
Reghunath A, Ghasi RG. Reghunath A, et al. Childs Nerv Syst. 2020 Jan;36(1):27-38. doi: 10.1007/s00381-019-04429-0. Epub 2019 Nov 27. Childs Nerv Syst. 2020. PMID: 31776716 Review.
REVIEW: We discuss the classification of MCD according to the embryologic stage of cerebral cortex at which the abnormality occurred and the unique imaging features of various malformations, including microcephaly, hemimegalencephaly, lissencephaly, focal cortical dysplasia, hete …
REVIEW: We discuss the classification of MCD according to the embryologic stage of cerebral cortex at which the abnormality occurred and the …
[Disorders of migration and gyration].
Pogledic I. Pogledic I. Radiologe. 2018 Jul;58(7):653-658. doi: 10.1007/s00117-018-0400-x. Radiologe. 2018. PMID: 29846745 Review. German.
Absent Cavum Septi Pellucidi.
Society for Maternal-Fetal Medicine (SMFM); Ward A, Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B23-B26. doi: 10.1016/j.ajog.2020.08.180. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168214 Review. No abstract available.
72 results