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

Year Number of Results
1963 1
1979 1
1984 1
1987 1
1988 1
1990 1
1994 1
1995 1
1997 1
1999 2
2000 2
2001 2
2002 1
2004 1
2005 4
2006 7
2007 1
2008 2
2009 6
2010 5
2011 4
2012 3
2013 9
2014 6
2015 5
2016 12
2017 16
2018 11
2019 7
2020 12
2021 13
2022 9
2023 8

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139 results

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Page 1
Rubella.
Winter AK, Moss WJ. Winter AK, et al. Lancet. 2022 Apr 2;399(10332):1336-1346. doi: 10.1016/S0140-6736(21)02691-X. Lancet. 2022. PMID: 35367004 Review.
Rubella is an acute illness caused by rubella virus and characterised by fever and rash. Although rubella is a clinically mild illness, primary rubella virus infection in early pregnancy can result in congenital rubella syndrome, which has serious medical and public health …
Rubella is an acute illness caused by rubella virus and characterised by fever and rash. Although rubella is a clinically mild illness, p
Microcephaly, an etiopathogenic vision.
Becerra-Solano LE, Mateos-Sánchez L, López-Muñoz E. Becerra-Solano LE, et al. Pediatr Neonatol. 2021 Jul;62(4):354-360. doi: 10.1016/j.pedneo.2021.05.008. Epub 2021 May 25. Pediatr Neonatol. 2021. PMID: 34112604 Free article. Review.
Microcephaly is defined by an occipital-frontal head circumference (OFD) 2 standard deviations (SD) smaller than the average expected for age, gender and population. ...The objective of this work is to review the available information and reinforce the proposal to carry ou
Microcephaly is defined by an occipital-frontal head circumference (OFD) 2 standard deviations (SD) smaller than the average expected
Imaging of Microcephaly.
Okafor C, Kanekar S. Okafor C, et al. Clin Perinatol. 2022 Sep;49(3):693-713. doi: 10.1016/j.clp.2022.04.004. Clin Perinatol. 2022. PMID: 36113930 Review.
Similarly, severe microcephaly is defined as an OFC that is less than three standard deviations below the average. Microcephaly is not a diagnosis, but rather, a finding that is secondary to a multitude of etiologies that can be categorized as prenatal versus postna …
Similarly, severe microcephaly is defined as an OFC that is less than three standard deviations below the average. Microcephaly
STIL balancing primary microcephaly and cancer.
Patwardhan D, Mani S, Passemard S, Gressens P, El Ghouzzi V. Patwardhan D, et al. Cell Death Dis. 2018 Jan 19;9(2):65. doi: 10.1038/s41419-017-0101-9. Cell Death Dis. 2018. PMID: 29352115 Free PMC article. Review.
The role played by the centriolar protein STIL is highly illustrative of this balance at different stages of life as deregulation of the human STIL gene expression has been associated with either insufficient brain development (primary microcephaly) or cancer, two c …
The role played by the centriolar protein STIL is highly illustrative of this balance at different stages of life as deregulation of the hum …
HIV neuropathology.
Morgello S. Morgello S. Handb Clin Neurol. 2018;152:3-19. doi: 10.1016/B978-0-444-63849-6.00002-5. Handb Clin Neurol. 2018. PMID: 29604982 Review.
Primary human immunodeficiency virus (HIV) neuropathologies can affect all levels of the neuraxis and occur in all stages of natural history disease. ...In pediatric patients, the spectrum of neuropathology is altered by the impacts of HIV on a developing nervous system, w
Primary human immunodeficiency virus (HIV) neuropathologies can affect all levels of the neuraxis and occur in all stages of natural
D-glyceric aciduria.
Dimer NW, Schuck PF, Streck EL, Ferreira GC. Dimer NW, et al. An Acad Bras Cienc. 2015 Aug;87(2 Suppl):1409-14. doi: 10.1590/0001-3765201520150021. Epub 2015 Aug 4. An Acad Bras Cienc. 2015. PMID: 26247153 Free article. Review.
The main clinical and neurological symptoms seen in affected patients include progressive encephalopathy, hypotonia, psychomotor and mental retardation, microcephaly, seizures, speech delay, metabolic acidosis, and even death. ...
The main clinical and neurological symptoms seen in affected patients include progressive encephalopathy, hypotonia, psychomotor and mental …
The Genetics of Primary Microcephaly.
Jayaraman D, Bae BI, Walsh CA. Jayaraman D, et al. Annu Rev Genomics Hum Genet. 2018 Aug 31;19:177-200. doi: 10.1146/annurev-genom-083117-021441. Epub 2018 May 23. Annu Rev Genomics Hum Genet. 2018. PMID: 29799801 Review.
Primary microcephaly (MCPH, for "microcephaly primary hereditary") is a disorder of brain development that results in a head circumference more than 3 standard deviations below the mean for age and gender. It has a wide variety of causes, including tox
Primary microcephaly (MCPH, for "microcephaly primary hereditary") is a disorder of brain development that resul
Multifaceted Microcephaly-Related Gene MCPH1.
Kristofova M, Ori A, Wang ZQ. Kristofova M, et al. Cells. 2022 Jan 14;11(2):275. doi: 10.3390/cells11020275. Cells. 2022. PMID: 35053391 Free PMC article. Review.
MCPH1, or BRIT1, is often mutated in human primary microcephaly type 1, a neurodevelopmental disorder characterized by a smaller brain size at birth, due to its dysfunction in regulating the proliferation and self-renewal of neuroprogenitor cells. ...
MCPH1, or BRIT1, is often mutated in human primary microcephaly type 1, a neurodevelopmental disorder characterized by a small …
Investigating microcephaly.
Woods CG, Parker A. Woods CG, et al. Arch Dis Child. 2013 Sep;98(9):707-13. doi: 10.1136/archdischild-2012-302882. Epub 2013 Jun 28. Arch Dis Child. 2013. PMID: 23814088 Review.
1. Microcephaly is a clinical finding, not a 'disease', and is a crude but trusted assessment of intracranial brain volume. 2. Developmental processes reducing in utero neuron generation present at birth with 'Primary microcephaly'. 3. 'Secondary microceph
1. Microcephaly is a clinical finding, not a 'disease', and is a crude but trusted assessment of intracranial brain volume. 2. Develo …
Microcephaly.
Passemard S, Kaindl AM, Verloes A. Passemard S, et al. Handb Clin Neurol. 2013;111:129-41. doi: 10.1016/B978-0-444-52891-9.00013-0. Handb Clin Neurol. 2013. PMID: 23622158 Review.
Primary non-syndromal microcephalies are recessive disorders resulting from abnormal control of mitotic spindle and cell cycle kinetics in progenitor cells. ...Genetic etiologies of developmental microcephalies are reviewed....
Primary non-syndromal microcephalies are recessive disorders resulting from abnormal control of mitotic spindle and cell cycle
139 results