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

Year Number of Results
1948 3
1951 2
1953 2
1956 1
1957 2
1958 2
1960 1
1961 5
1962 3
1963 4
1964 7
1965 1
1966 5
1967 1
1968 6
1969 4
1970 3
1971 2
1972 6
1973 4
1974 6
1975 2
1976 4
1977 4
1978 9
1979 4
1980 4
1981 8
1982 13
1983 9
1984 6
1985 10
1986 3
1987 13
1988 9
1989 11
1990 11
1991 17
1992 8
1993 12
1994 7
1995 12
1996 19
1997 10
1998 15
1999 21
2000 23
2001 14
2002 18
2003 26
2004 25
2005 28
2006 30
2007 30
2008 28
2009 42
2010 45
2011 52
2012 58
2013 68
2014 71
2015 84
2016 79
2017 89
2018 69
2019 99
2020 121
2021 118
2022 105
2023 106
2024 24

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1,577 results

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Page 1
In regard to Cabezas-Camarero et al.
Yilmaz MT, Yuce Sari S, Yazici G. Yilmaz MT, et al. Anticancer Drugs. 2023 Nov 1;34(10):1202-1204. doi: 10.1097/CAD.0000000000001511. Epub 2023 Oct 11. Anticancer Drugs. 2023. PMID: 37823285 No abstract available.
Nina Cabezas Wallscheid: Enjoying the freedom to decide my research path.
Van Emmenis L. Van Emmenis L. J Exp Med. 2023 Oct 2;220(10):e20231561. doi: 10.1084/jem.20231561. Epub 2023 Sep 19. J Exp Med. 2023. PMID: 37725354 Free PMC article.
Nina Cabezas Wallscheid is a group leader at the Max Planck Institute of Immunobiology and Epigenetics in Freiburg, Germany. ...
Nina Cabezas Wallscheid is a group leader at the Max Planck Institute of Immunobiology and Epigenetics in Freiburg, Germany. ...
Genome-first approach diagnosed Cabezas syndrome via novel CUL4B mutation detection.
Okamoto N, Watanabe M, Naruto T, Matsuda K, Kohmoto T, Saito M, Masuda K, Imoto I. Okamoto N, et al. Hum Genome Var. 2017 Jan 19;4:16045. doi: 10.1038/hgv.2016.45. eCollection 2017. Hum Genome Var. 2017. PMID: 28144446 Free PMC article.
Cabezas syndrome is a syndromic form of X-linked intellectual disability primarily characterized by a short stature, hypogonadism and abnormal gait, with other variable features resulting from mutations in the CUL4B gene. ...(Glu900*)] in the last coding exon of CUL4B, thu
Cabezas syndrome is a syndromic form of X-linked intellectual disability primarily characterized by a short stature, hypogonadism and
Historical Lattice Trees.
Cabezas M, Fribergh A, Holmes M, Perkins E. Cabezas M, et al. Commun Math Phys. 2023;401(1):435-496. doi: 10.1007/s00220-023-04641-9. Epub 2023 Jan 31. Commun Math Phys. 2023. PMID: 37360187 Free PMC article.
[Medical and health care in Peru].
Cabezas C. Cabezas C. Rev Peru Med Exp Salud Publica. 2019 Apr-Jun;36(2):165-166. doi: 10.17843/rpmesp.2019.362.4620. Epub 2019 Aug 22. Rev Peru Med Exp Salud Publica. 2019. PMID: 31460626 Spanish. No abstract available.
Importance of Genetic Diagnosis in Global Developmental Delay: A Case of Cabezas Syndrome Caused by CUL4B Gene Deletion and Not Identified by Array-CHG.
Magalhães TL, Viegas MV, Mendonça C, Travessa A, Soares D. Magalhães TL, et al. Cureus. 2023 Sep 26;15(9):e46010. doi: 10.7759/cureus.46010. eCollection 2023 Sep. Cureus. 2023. PMID: 37900499 Free PMC article.
We report a case of a 10-year-old boy with ID and GDD who was diagnosed with Cabezas syndrome, a rare genetic disorder caused by a deletion of the CUL4B gene. ...
We report a case of a 10-year-old boy with ID and GDD who was diagnosed with Cabezas syndrome, a rare genetic disorder caused by a de …
[COVID-19 pandemic: storms and challenges].
Cabezas C. Cabezas C. Rev Peru Med Exp Salud Publica. 2020 Oct-Dec;37(4):603-604. doi: 10.17843/rpmesp.2020.374.6866. Epub 2021 Feb 3. Rev Peru Med Exp Salud Publica. 2020. PMID: 33566897 Spanish. No abstract available.
1-(Phenyl-sulfon-yl)-1H-indole-2-carbaldehyde.
Pineda LW, Ferllini N, Cabezas JA. Pineda LW, et al. IUCrdata. 2022 Apr 22;7(Pt 4):x220401. doi: 10.1107/S2414314622004011. eCollection 2022 Apr. IUCrdata. 2022. PMID: 36337686 Free PMC article.
1,577 results