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

Year Number of Results
1981 1
1982 1
1984 1
1985 1
1986 4
1987 3
1988 9
1989 8
1990 9
1991 8
1992 5
1993 14
1994 13
1995 14
1996 9
1997 10
1998 14
1999 9
2000 9
2001 21
2002 17
2003 13
2004 15
2005 17
2006 16
2007 18
2008 15
2009 23
2010 16
2011 17
2012 16
2013 20
2014 22
2015 13
2016 34
2017 29
2018 25
2019 19
2020 32
2021 24
2022 34
2023 32
2024 8

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573 results

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Page 1
Septo-optic dysplasia.
Sataite I, Cudlip S, Jayamohan J, Ganau M. Sataite I, et al. Handb Clin Neurol. 2021;181:51-64. doi: 10.1016/B978-0-12-820683-6.00005-1. Handb Clin Neurol. 2021. PMID: 34238479 Review.
Septo-optic dysplasia (SOD) or de Morsier's syndrome is a rare congenital disorder characterized by a classic triad of: (a) optic nerve hypoplasia, (b) agenesis of septum pellucidum and corpus callosum, and (c) hypoplasia of the hypothalamic-pituitary …
Septo-optic dysplasia (SOD) or de Morsier's syndrome is a rare congenital disorder characterized by a classic triad of: (a) optic nerve h …
Phenylketonuria and the brain.
Rovelli V, Longo N. Rovelli V, et al. Mol Genet Metab. 2023 May;139(1):107583. doi: 10.1016/j.ymgme.2023.107583. Epub 2023 Apr 15. Mol Genet Metab. 2023. PMID: 37105048 Review.
During fetal life, high levels of phenylalanine such as those seen in maternal PKU can result in microcephaly, neuronal loss and corpus callosum hypoplasia. Elevated phenylalanine levels during the first few years of life can cause acquired microcephaly, seve …
During fetal life, high levels of phenylalanine such as those seen in maternal PKU can result in microcephaly, neuronal loss and corpus …
Tubulin mutations in human neurodevelopmental disorders.
Maillard C, Roux CJ, Charbit-Henrion F, Steffann J, Laquerriere A, Quazza F, Buisson NB. Maillard C, et al. Semin Cell Dev Biol. 2023 Mar 15;137:87-95. doi: 10.1016/j.semcdb.2022.07.009. Epub 2022 Jul 30. Semin Cell Dev Biol. 2023. PMID: 35915025 Review.
Additional distinctive MRI features include dysmorphism of the basal ganglia, midline commissural structure hypoplasia or agenesis, and cerebellar and brainstem hypoplasia. Tubulinopathies can be diagnosed as early as 21-24 gestational weeks using imaging and neurop …
Additional distinctive MRI features include dysmorphism of the basal ganglia, midline commissural structure hypoplasia or agenesis, a …
Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
D'Antonio F, Pagani G, Familiari A, Khalil A, Sagies TL, Malinger G, Leibovitz Z, Garel C, Moutard ML, Pilu G, Bhide A, Acharya G, Leombroni M, Manzoli L, Papageorghiou A, Prefumo F. D'Antonio F, et al. Pediatrics. 2016 Sep;138(3):e20160445. doi: 10.1542/peds.2016-0445. Pediatrics. 2016. PMID: 27581855 Review.
CONTEXT: Antenatal counseling in cases of agenesis of the corpus callosum (ACC) is challenging. OBJECTIVES: To ascertain the outcome in fetuses with isolated complete ACC and partial ACC. ...STUDY SELECTION: Studies reporting a prenatal diagnosis of ACC. The outcome …
CONTEXT: Antenatal counseling in cases of agenesis of the corpus callosum (ACC) is challenging. OBJECTIVES: To ascertain the o …
[Structural and functional neuroanatomy of attention-deficit hyperactivity disorder (ADHD)].
Emond V, Joyal C, Poissant H. Emond V, et al. Encephale. 2009 Apr;35(2):107-14. doi: 10.1016/j.encep.2008.01.005. Epub 2008 Jul 7. Encephale. 2009. PMID: 19393378 Review. French.
This network involves the lateral prefrontal cortex, the dorsal anterior cingulate cortex, the caudate nucleus and putamen. Moreover, a growing literature demonstrates abnormalities affecting other cortical regions and the cerebellum. The exploratory brain regions of inter …
This network involves the lateral prefrontal cortex, the dorsal anterior cingulate cortex, the caudate nucleus and putamen. Moreover, a grow …
Hypoplasia of the Corpus Callosum: A Single Center Experience and a Concise Literature Review.
D'Ambrosio V, Boccherini C, Manganaro L, Panici PB, Cellitti R, Vena F, Pajno C, Corno S, Brunelli R, Giancotti A. D'Ambrosio V, et al. Fetal Pediatr Pathol. 2021 Dec;40(6):626-637. doi: 10.1080/15513815.2020.1723148. Epub 2020 Feb 18. Fetal Pediatr Pathol. 2021. PMID: 32070177 Review.
AimCorpus callosum hypoplasia is described as a fully formed corpus callosum with reduced thickness. ...Methods: PubMed, Medline and reference lists were searched using combinations of these terms: "Hypoplasia of corpus callosum an …
AimCorpus callosum hypoplasia is described as a fully formed corpus callosum with reduced thickness. ...Methods: …
Agenesis of the corpus callosum: What to tell expecting parents?
Tsai P, Shinar S. Tsai P, et al. Prenat Diagn. 2023 Nov;43(12):1527-1535. doi: 10.1002/pd.6447. Epub 2023 Oct 4. Prenat Diagn. 2023. PMID: 37794643 Review.
Agenesis of the corpus callosum (ACC) is one of the most common brain malformations, with an incidence estimated to range from 0.5 to 70 in 10,000 among the general population. Prenatal diagnosis is made via ultrasound; however, fetal MRI is useful to confirm or exc …
Agenesis of the corpus callosum (ACC) is one of the most common brain malformations, with an incidence estimated to range from …
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.
Recent advances in prenatal imaging have resulted in an increasing rate of prenatal diagnosis of abnormalities of the posterior fossa including rhombencephalosynapsis. ...The most common associated findings with rhombencephalosynapsis include hydrocephalus, mesencephalosyn …
Recent advances in prenatal imaging have resulted in an increasing rate of prenatal diagnosis of abnormalities of the posterior fossa …
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.
BACKGROUND: Septo-optic dysplasia (SOD), once a variable triad of septum pellucidum defects (SPDs), optic nerve hypoplasia (ONH), and hypopituitarism, has had multiple findings added, with uncertain causes, definitions, and limits. ...Disruption by-products can affect deve …
BACKGROUND: Septo-optic dysplasia (SOD), once a variable triad of septum pellucidum defects (SPDs), optic nerve hypoplasia (ONH), and …
[Dandy-Walker malformation].
Reith W, Haussmann A. Reith W, et al. Radiologe. 2018 Jul;58(7):629-635. doi: 10.1007/s00117-018-0403-7. Radiologe. 2018. PMID: 29797040 Review. German.
The Dandy-Walker malformation is the most frequent cerebral malformation. It is defined by hypoplasia and upward rotation of the vermis cerebelli, a cystic enlargement of the fourth ventricle and in total an enlarged posterior fossa with cranially shifted position of the l …
The Dandy-Walker malformation is the most frequent cerebral malformation. It is defined by hypoplasia and upward rotation of the verm …
573 results