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

Year Number of Results
1964 1
1965 1
1966 1
1967 2
1968 16
1969 5
1970 5
1971 14
1972 17
1973 16
1974 21
1975 24
1976 19
1977 10
1978 14
1979 15
1980 14
1981 25
1982 17
1983 22
1984 26
1985 35
1986 49
1987 51
1988 91
1989 85
1990 108
1991 128
1992 147
1993 166
1994 132
1995 168
1996 171
1997 201
1998 231
1999 278
2000 321
2001 312
2002 303
2003 303
2004 341
2005 341
2006 370
2007 383
2008 402
2009 411
2010 455
2011 492
2012 515
2013 535
2014 523
2015 437
2016 411
2017 387
2018 394
2019 332
2020 323
2021 263
2022 224
2023 202
2024 62

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10,352 results

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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 …
Midbrain, Pons, and Medulla: Anatomy and Syndromes.
Sciacca S, Lynch J, Davagnanam I, Barker R. Sciacca S, et al. Radiographics. 2019 Jul-Aug;39(4):1110-1125. doi: 10.1148/rg.2019180126. Radiographics. 2019. PMID: 31283463 Review.
The anatomy of the brainstem is complex. It contains numerous cranial nerve nuclei and is traversed by multiple tracts between the brain and spinal cord. ...These syndromes can have subtle imaging findings that may be missed by a radiologist unfamiliar with the a …
The anatomy of the brainstem is complex. It contains numerous cranial nerve nuclei and is traversed by multiple tracts between the …
Neuroscience and Sex/Gender: Looking Back and Forward.
Hines M. Hines M. J Neurosci. 2020 Jan 2;40(1):37-43. doi: 10.1523/JNEUROSCI.0750-19.2019. Epub 2019 Sep 5. J Neurosci. 2020. PMID: 31488609 Free PMC article. Review.
In addition to influencing behavior, testosterone and hormones produced from testosterone affect mammalian brain structure. Studies using human autopsy material have found some sex differences in the human brain similar to those seen in other species, and have repor …
In addition to influencing behavior, testosterone and hormones produced from testosterone affect mammalian brain structure. Studies u …
Dandy-Walker Malformation.
Society for Maternal-Fetal Medicine (SMFM); Monteagudo A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B38-B41. doi: 10.1016/j.ajog.2020.08.184. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168220 Review. No abstract available.
Neurocutaneous syndromes.
Klar N, Cohen B, Lin DDM. Klar N, et al. Handb Clin Neurol. 2016;135:565-589. doi: 10.1016/B978-0-444-53485-9.00027-1. Handb Clin Neurol. 2016. PMID: 27432683 Review.
Neurocutaneous syndromes (or phakomatoses) are a diverse group of congenital disorders that encompass abnormalities of neuroectodermal and, sometimes, mesodermal development, hence commonly involving the skin, eye, and central nervous system. These are often inherit …
Neurocutaneous syndromes (or phakomatoses) are a diverse group of congenital disorders that encompass abnormalities of neuroec …
Neuropathology of holoprosencephaly.
Fallet-Bianco C. Fallet-Bianco C. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):214-228. doi: 10.1002/ajmg.c.31623. Am J Med Genet C Semin Med Genet. 2018. PMID: 30182440 Review.
Although the term "HPE" suggests a disorder affecting only the prosencephalon, other brain structures are involved, underlining the complexity of the malformation. Because of close spatiotemporal interactions and common signaling pathways contributing to the development of …
Although the term "HPE" suggests a disorder affecting only the prosencephalon, other brain structures are involved, underlining the c …
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 …
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 …
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 …
The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies.
Van De Weghe JC, Gomez A, Doherty D. Van De Weghe JC, et al. Annu Rev Genomics Hum Genet. 2022 Aug 31;23:301-329. doi: 10.1146/annurev-genom-121321-093528. Epub 2022 Jun 2. Annu Rev Genomics Hum Genet. 2022. PMID: 35655331 Free PMC article. Review.
Ciliary dysfunction causes many human conditions termed ciliopathies, which range from multiple congenital malformations to adult-onset single-organ failure. Research on the genetics of the JS-MKS-NPH spectrum has spurred extensive functional work exploring the broadly imp …
Ciliary dysfunction causes many human conditions termed ciliopathies, which range from multiple congenital malformations to adult-ons …
10,352 results
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