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

Year Number of Results
1972 1
1974 1
1979 1
1981 4
1982 2
1983 2
1985 2
1986 1
1987 1
1988 3
1989 2
1990 7
1991 3
1992 1
1993 5
1994 6
1995 4
1996 2
1997 1
1998 2
1999 6
2000 4
2001 7
2002 5
2003 2
2004 2
2005 8
2006 2
2007 6
2008 8
2009 10
2010 6
2011 6
2012 7
2013 10
2014 6
2015 5
2016 5
2017 3
2018 9
2019 6
2020 8
2021 4
2022 8
2023 3
2024 1

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182 results

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Page 1
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.
[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. ...The current description as Dandy-Walker malformation was introduced in 1954 by Bender. In addition to these classical findings, the Dandy-Walker malformation is …
The Dandy-Walker malformation is the most frequent cerebral malformation. ...The current description as Dandy-Walker …
Fetal cerebellar disorders.
Lerman-Sagie T, Prayer D, Stöcklein S, Malinger G. Lerman-Sagie T, et al. Handb Clin Neurol. 2018;155:3-23. doi: 10.1016/B978-0-444-64189-2.00001-9. Handb Clin Neurol. 2018. PMID: 29891067 Review.
Neurocutaneous melanocytosis.
Flores-Sarnat L. Flores-Sarnat L. Handb Clin Neurol. 2013;111:369-88. doi: 10.1016/B978-0-444-52891-9.00042-7. Handb Clin Neurol. 2013. PMID: 23622187 Review.
The neurological manifestations often appear in infancy.The special association of neurocutaneous melanosis with Dandy-Walker malformation complex may be explained by a common pathogenesis. ...
The neurological manifestations often appear in infancy.The special association of neurocutaneous melanosis with Dandy-Walker …
Prenatal diagnosis of Emanuel syndrome - case series and review of the literature.
Piwowarczyk P, Massalska D, Obodzińska I, Gawlik Zawiślak S, Bijok J, Kucińska-Chahwan A, Roszkowski T. Piwowarczyk P, et al. J Obstet Gynaecol. 2022 Oct;42(7):2615-2620. doi: 10.1080/01443615.2022.2114331. Epub 2022 Sep 1. J Obstet Gynaecol. 2022. PMID: 36048922 Review.
Defects of the posterior fossa (62% of foetuses; 13/21) and left diaphragmatic hernia (29% of foetuses; 6/21) are the most frequently reported prenatal findings in ES syndrome. No pattern of specific prenatal ultrasound markers of ES exists. ...Specific diagnosis can be ma …
Defects of the posterior fossa (62% of foetuses; 13/21) and left diaphragmatic hernia (29% of foetuses; 6/21) are the most frequently report …
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.
Fetal Ventriculomegaly.
Society for Maternal-Fetal Medicine (SMFM); Norton ME, Fox NS, Monteagudo A, Kuller JA, Craigo S. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2020 Dec;223(6):B30-B33. doi: 10.1016/j.ajog.2020.08.182. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168210 Review. No abstract available.
Dandy-Walker syndrome associated with syringomyelia in an adult: a case report and literature review.
Zhang N, Qi Z, Zhang X, Zhong F, Yao H, Xu X, Liu J, Huang Y. Zhang N, et al. J Int Med Res. 2019 Apr;47(4):1771-1777. doi: 10.1177/0300060518808961. Epub 2019 Feb 24. J Int Med Res. 2019. PMID: 30799663 Free PMC article. Review.
Dandy-Walker syndrome associated with syringomyelia is a rare condition, with few reports of adult cases. ...Magnetic resonance imaging showed that syringomyelia was greatly reduced and the hydrocephalus remained unchanged. Dandy-Walker syndr …
Dandy-Walker syndrome associated with syringomyelia is a rare condition, with few reports of adult cases. ...Magnetic r …
Kabuki syndrome: novel pathogenic variants, new phenotypes and review of literature.
Shangguan H, Su C, Ouyang Q, Cao B, Wang J, Gong C, Chen R. Shangguan H, et al. Orphanet J Rare Dis. 2019 Nov 14;14(1):255. doi: 10.1186/s13023-019-1219-x. Orphanet J Rare Dis. 2019. PMID: 31727177 Free PMC article. Review.
OBJECTIVE: This study describes 5 novel variants of 7 KMT2D/KDM6A gene and summarizes the clinical manifestations and the mutational spectrum of 47 Chinese Kabuki syndrome (KS) patients. METHODS: Blood samples were collected for whole-exome sequencing (WES) for 7 patients …
OBJECTIVE: This study describes 5 novel variants of 7 KMT2D/KDM6A gene and summarizes the clinical manifestations and the mutational spectru …
Posterior fossa malformations.
Shekdar K. Shekdar K. Semin Ultrasound CT MR. 2011 Jun;32(3):228-41. doi: 10.1053/j.sult.2011.02.003. Semin Ultrasound CT MR. 2011. PMID: 21596278 Review.
Disorders associated with a large posterior fossa include classic Dandy-Walker malformation, Blake's pouch cyst, mega cisterna magna, and posterior fossa arachnoid cyst. Disorders associated with normal or small posterior fossa include Dandy-Walker var …
Disorders associated with a large posterior fossa include classic Dandy-Walker malformation, Blake's pouch cyst, mega cisterna …
182 results