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Year Number of Results
1815 1
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1857 1
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1882 3
1885 1
1886 1
1890 1
1909 1
1919 1
1920 1
1922 1
1927 1
1941 1
1946 3
1947 5
1948 6
1949 3
1950 3
1951 6
1952 3
1953 8
1954 3
1955 3
1956 4
1957 6
1958 3
1959 3
1960 5
1962 4
1963 4
1964 7
1965 8
1966 7
1967 3
1968 8
1969 7
1970 7
1971 11
1972 10
1973 14
1974 13
1975 26
1976 13
1977 26
1978 20
1979 19
1980 13
1981 15
1982 11
1983 17
1984 14
1985 22
1986 28
1987 17
1988 30
1989 21
1990 23
1991 27
1992 37
1993 35
1994 40
1995 38
1996 45
1997 65
1998 59
1999 66
2000 56
2001 73
2002 70
2003 80
2004 75
2005 69
2006 94
2007 107
2008 87
2009 85
2010 93
2011 83
2012 114
2013 137
2014 135
2015 123
2016 141
2017 125
2018 138
2019 157
2020 152
2021 195
2022 198
2023 158
2024 53

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The following term was not found in PubMed: etnovia
Page 1
Showing results for coffin etnovia
Your search for coffein-etnovia retrieved no results
Genotype-Phenotype Correlations in 208 Individuals with Coffin-Siris Syndrome.
Vasko A, Drivas TG, Schrier Vergano SA. Vasko A, et al. Genes (Basel). 2021 Jun 19;12(6):937. doi: 10.3390/genes12060937. Genes (Basel). 2021. PMID: 34205270 Free PMC article.
Coffin-Siris syndrome (CSS, MIM 135900) is a multi-system intellectual disability syndrome characterized by classic dysmorphic features, developmental delays, and organ system anomalies. ...
Coffin-Siris syndrome (CSS, MIM 135900) is a multi-system intellectual disability syndrome characterized by classic dysmorphic featur …
Coffin-Lowry syndrome.
Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A. Pereira PM, et al. Eur J Hum Genet. 2010 Jun;18(6):627-33. doi: 10.1038/ejhg.2009.189. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888300 Free PMC article. Review.
Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation, which is characterized in male patients by psychomotor and growth retardation and various skeletal anomalies. ...
Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation, which is characterized in male patients by psychomoto …
Digestive motility disorders.
Coffin B. Coffin B. J Visc Surg. 2022 Mar;159(1S):S1-S2. doi: 10.1016/j.jviscsurg.2022.01.004. Epub 2022 Feb 2. J Visc Surg. 2022. PMID: 35123907 No abstract available.
Coffin-Siris syndrome and epilepsy.
Curcio MR, Ferranti S, Lotti F, Grosso S. Curcio MR, et al. Neurol Sci. 2021 Feb;42(2):727-729. doi: 10.1007/s10072-020-04782-y. Epub 2020 Oct 2. Neurol Sci. 2021. PMID: 33006724
Coffin-Siris syndrome is a rare genetic disorder defined by the presence of particular facial traits, congenital malformations, intellectual disability, and speech impairment. Epilepsy in Coffin-Siris syndrome has only occasionally been reported, and its features ar …
Coffin-Siris syndrome is a rare genetic disorder defined by the presence of particular facial traits, congenital malformations, intel …
Premature burial.
Byard RW. Byard RW. Forensic Sci Med Pathol. 2023 Dec;19(4):625-628. doi: 10.1007/s12024-023-00644-z. Epub 2023 May 17. Forensic Sci Med Pathol. 2023. PMID: 37195590 Free PMC article.
In previous centuries however, reports of live burials were frequently promulgated in the media fostering an industry focused around the manufacturing and selling of security coffins which either facilitated egress or enabled the recently buried to alert those on the surfa …
In previous centuries however, reports of live burials were frequently promulgated in the media fostering an industry focused around the man …
[Coffin-Lowry syndrome].
Guitti JC, Peres FF. Guitti JC, et al. J Pediatr (Rio J). 2000 Jul-Aug;76(4):305-9. doi: 10.2223/jped.8. J Pediatr (Rio J). 2000. PMID: 14647661 Portuguese.
OBJECTIVE: To promote the diffusion of the knowledge on the Coffin-Lowry syndrome and to contribute to the outline of the disease.METHODS: Case report.RESULTS: The clinical signs of a patient with the Coffin-Lowry syndrome are described and discussed.CONCLUSIONS: Th …
OBJECTIVE: To promote the diffusion of the knowledge on the Coffin-Lowry syndrome and to contribute to the outline of the disease.MET …
Coffin-Lowry syndrome.
Ahuja SR, Upadhye S, Kulkarni HV, Kulkarni MV. Ahuja SR, et al. Indian J Pediatr. 2003 Dec;70(12):1001-2. doi: 10.1007/BF02723830. Indian J Pediatr. 2003. PMID: 14719793
The Coffin-Lowry syndrome is an established syndrome of severe mental and growth retardation, characteristic dysmorphic features and skeletal anomalies. ...
The Coffin-Lowry syndrome is an established syndrome of severe mental and growth retardation, characteristic dysmorphic features and …
Coffin-Siris syndrome.
Barber N, Say B. Barber N, et al. Am J Dis Child. 1978 Oct;132(10):1044. doi: 10.1001/archpedi.1978.02120350112028. Am J Dis Child. 1978. PMID: 717300 No abstract available.
Overdose Research: 15 Years Later.
Coffin PO, Rich JD. Coffin PO, et al. J Urban Health. 2019 Feb;96(1):1-5. doi: 10.1007/s11524-018-00344-y. J Urban Health. 2019. PMID: 30623291 Free PMC article. No abstract available.
Pigmentation abnormalities in Coffin-Siris syndrome.
Zapata-Aldana E, Ceballos-Sáenz D, Vásquez-Ríos JR, Vera-Alvarez L, Carrillo-Soler J. Zapata-Aldana E, et al. Clin Genet. 2023 Sep;104(3):393-394. doi: 10.1111/cge.14356. Epub 2023 May 11. Clin Genet. 2023. PMID: 37166055
Pigmentary abnormalities in Coffin-Siris Syndrome should be considered as part of the wide phenotypical spectrum of this patients....
Pigmentary abnormalities in Coffin-Siris Syndrome should be considered as part of the wide phenotypical spectrum of this patients....
3,416 results