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

Year Number of Results
1946 1
1948 2
1952 1
1953 1
1954 2
1956 1
1957 2
1958 3
1959 1
1960 1
1961 4
1964 1
1965 3
1966 8
1967 10
1968 26
1969 26
1970 25
1971 47
1972 30
1973 29
1974 52
1975 77
1976 53
1977 70
1978 65
1979 77
1980 64
1981 77
1982 88
1983 91
1984 103
1985 148
1986 184
1987 182
1988 202
1989 238
1990 340
1991 304
1992 349
1993 454
1994 420
1995 515
1996 499
1997 569
1998 618
1999 625
2000 688
2001 802
2002 693
2003 739
2004 823
2005 830
2006 975
2007 996
2008 1107
2009 1035
2010 1064
2011 1176
2012 1178
2013 1282
2014 1319
2015 1221
2016 884
2017 814
2018 825
2019 841
2020 813
2021 599
2022 518
2023 466
2024 147

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25,651 results

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Quoted phrase not found in phrase index: "Abnormality of brain morphology"
Page 1
Craniosynostosis - Recognition, clinical characteristics, and treatment.
Kajdic N, Spazzapan P, Velnar T. Kajdic N, et al. Bosn J Basic Med Sci. 2018 May 20;18(2):110-116. doi: 10.17305/bjbms.2017.2083. Bosn J Basic Med Sci. 2018. PMID: 28623672 Free PMC article. Review.
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped skull. The main cause of craniosynostosis is premature closure of one or more cranial sutures. ...When left untreated, craniosynostosis can c …
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped s …
Neuronal Migration Disorders.
Roberts B. Roberts B. Radiol Technol. 2018 Jan;89(3):279-295. Radiol Technol. 2018. PMID: 29298944 Review.
Enhanced understanding of brain development has led to increased awareness of the links between disorders of neuronal migration and seizure disorders. ...
Enhanced understanding of brain development has led to increased awareness of the links between disorders of neuronal migration and s …
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA Jr, Kim R, Bilguvar K, López-Giráldez F, Tikhonova I, Mane S, Romano-Adesman A, Qi H, Vardarajan B, Ma L, Daly M, Roberts AE, Russell MW, Mital S, Newburger JW, Gaynor JW, Breitbart RE, Iossifov I, Ronemus M, Sanders SJ, Kaltman JR, Seidman JG, Brueckner M, Gelb BD, Goldmuntz E, Lifton RP, Seidman CE, Chung WK. Homsy J, et al. Science. 2015 Dec 4;350(6265):1262-6. doi: 10.1126/science.aac9396. Science. 2015. PMID: 26785492 Free PMC article.
Congenital heart disease (CHD) patients have an increased prevalence of extracardiac congenital anomalies (CAs) and risk of neurodevelopmental disabilities (NDDs). Exome sequencing of 1213 CHD parent-offspring trios identified an excess of protein-damaging de novo m …
Congenital heart disease (CHD) patients have an increased prevalence of extracardiac congenital anomalies (CAs) and risk of ne …
Walker-Warburg syndrome.
Vajsar J, Schachter H. Vajsar J, et al. Orphanet J Rare Dis. 2006 Aug 3;1:29. doi: 10.1186/1750-1172-1-29. Orphanet J Rare Dis. 2006. PMID: 16887026 Free PMC article. Review.
Walker-Warburg Syndrome (WWS) is a rare form of autosomal recessive congenital muscular dystrophy associated with brain and eye abnormalities. ...It is associated with type II cobblestone lissencephaly, hydrocephalus, cerebellar malformations, eye abnormal …
Walker-Warburg Syndrome (WWS) is a rare form of autosomal recessive congenital muscular dystrophy associated with brain and ey …
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. Patients with rhombencephalosynapsis may present with motor developmental delay, ataxia, swallowing diffi …
Recent advances in prenatal imaging have resulted in an increasing rate of prenatal diagnosis of abnormalities of the posterior fossa …
Acalvaria.
Hawasli AH, Beaumont TL, Vogel TW, Woo AS, Leonard JR. Hawasli AH, et al. J Neurosurg Pediatr. 2014 Aug;14(2):200-2. doi: 10.3171/2014.5.PEDS13688. Epub 2014 Jun 13. J Neurosurg Pediatr. 2014. PMID: 24926969
Acalvaria is a rare congenital malformation characterized by an absence of skin and skull. ...Upon delivery, the child was noted to have a frontal encephalocele and an absence of calvaria including skull and skin overlying the brain. A thin membrane representing dur …
Acalvaria is a rare congenital malformation characterized by an absence of skin and skull. ...Upon delivery, the child was noted to h …
Disorders of Ventral Induction/Spectrum of Holoprosencephaly.
Calloni SF, Caschera L, Triulzi FM. Calloni SF, et al. Neuroimaging Clin N Am. 2019 Aug;29(3):411-421. doi: 10.1016/j.nic.2019.03.003. Epub 2019 Apr 13. Neuroimaging Clin N Am. 2019. PMID: 31256862 Review.
Disorders of the ventral induction give rise to a group of congenital malformations that share in common the failure of the prosencephalon cleavage and subsequent formation of midline structures, presenting with a wide spectrum of severity. ...
Disorders of the ventral induction give rise to a group of congenital malformations that share in common the failure of the prosencep …
Brainstem dysgenesis: beyond Moebius syndrome.
Munell F, Tormos MA, Roig-Quilis M. Munell F, et al. Rev Neurol. 2018 Apr 1;66(7):241-250. Rev Neurol. 2018. PMID: 29557550 Free article. Review. English, Spanish.
Brainstem dysgenesis designates all those patients with congenital dysfunction of cranial nerves and muscle tone due to prenatal lesions or malformations of the brainstem. ...
Brainstem dysgenesis designates all those patients with congenital dysfunction of cranial nerves and muscle tone due to prenatal lesi …
Neu Laxova syndrome.
Dwivedi T, Gosavi M. Dwivedi T, et al. Indian J Pathol Microbiol. 2019 Jan-Mar;62(1):149-152. doi: 10.4103/IJPM.IJPM_351_17. Indian J Pathol Microbiol. 2019. PMID: 30706883
NeuLaxova syndrome (NLS) is a rare congenital abnormality involving multiple systems. Until date, only 60 cases of this syndrome have been reported in the literature. ...On dissection, all organs were in situ. Both lungs were hypoplastic, brain was atrophied, …
NeuLaxova syndrome (NLS) is a rare congenital abnormality involving multiple systems. Until date, only 60 cases of this syndro …
Fetal Brain Development in Congenital Heart Disease.
Peyvandi S, Rollins C. Peyvandi S, et al. Can J Cardiol. 2023 Feb;39(2):115-122. doi: 10.1016/j.cjca.2022.09.020. Epub 2022 Sep 27. Can J Cardiol. 2023. PMID: 36174913 Free PMC article. Review.
With the advent of fetal brain MRI, these brain abnormalities are now documented as they begin in utero, as early as the third trimester. ...The causes of abnormal fetal brain development are multifactorial and include cardiovascular physiology, …
With the advent of fetal brain MRI, these brain abnormalities are now documented as they begin in utero, as early as th …
25,651 results
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