Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1958 1
1961 1
1964 11
1965 7
1966 1
1967 7
1968 7
1969 13
1970 19
1971 27
1972 16
1973 15
1974 20
1975 21
1976 16
1977 34
1978 27
1979 42
1980 24
1981 49
1982 44
1983 61
1984 69
1985 77
1986 76
1987 66
1988 75
1989 102
1990 101
1991 81
1992 94
1993 116
1994 138
1995 136
1996 127
1997 116
1998 110
1999 136
2000 117
2001 167
2002 157
2003 171
2004 145
2005 173
2006 199
2007 203
2008 211
2009 236
2010 249
2011 229
2012 253
2013 277
2014 265
2015 289
2016 238
2017 236
2018 247
2019 234
2020 249
2021 227
2022 188
2023 160
2024 64

Text availability

Article attribute

Article type

Publication date

Search Results

6,519 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Abnormal cerebral signs in the newborn"
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. ...Thus, early diagnosis, expert surgic …
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped s …
Acalvaria.
Hawasli AH, Beaumont TL, Vogel TW, Woo AS, Leonard JR. Hawasli AH, et al. J Neurosurg Pediatr. 2014 Aug;14(2):200-2. doi: 10.3171/2014.5.PEDS13688. Epub 2014 Jun 13. J Neurosurg Pediatr. 2014. PMID: 24926969
Acalvaria is a rare congenital malformation characterized by an absence of skin and skull. The authors describe a newborn at an estimated 38 weeks gestational age who was delivered via cesarean section from a 32-year-old mother. ...
Acalvaria is a rare congenital malformation characterized by an absence of skin and skull. The authors describe a newborn at a …
Imaging the fetus and the newborn.
Hüppi PS. Hüppi PS. Top Magn Reson Imaging. 2011 Feb;22(1):1. doi: 10.1097/RMR.0b013e3182416f92. Top Magn Reson Imaging. 2011. PMID: 22186900 No abstract available.
Imaging of the Newborn Brain.
Barkovich AJ. Barkovich AJ. Semin Pediatr Neurol. 2019 Dec;32:100766. doi: 10.1016/j.spen.2019.08.002. Epub 2019 Sep 6. Semin Pediatr Neurol. 2019. PMID: 31813522 Review.
Neuroimaging enables the evaluation of many aspects of brain maturation, and detection of abnormalities such as malformation and injury. ...This paper reviews techniques to optimize assessment of maturity of the neonatal brain, as well as abnormalities …
Neuroimaging enables the evaluation of many aspects of brain maturation, and detection of abnormalities such as malformation a …
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 …
Neu Laxova syndrome.
Dwivedi T, Gosavi M. Dwivedi T, et al. Indian J Pathol Microbiol. 2019 Jan-Mar;62(1):149-152. doi: 10.4103/IJPM.IJPM_351_17. Indian J Pathol Microbiol. 2019. PMID: 30706883
NeuLaxova syndrome (NLS) is a rare congenital abnormality involving multiple systems. Until date, only 60 cases of this syndrome have been reported in the literature. ...Early diagnosis of the disease may offer termination of the pregnancy as an option. ...
NeuLaxova syndrome (NLS) is a rare congenital abnormality involving multiple systems. Until date, only 60 cases of this syndro …
Brainstem dysgenesis: beyond Moebius syndrome.
Munell F, Tormos MA, Roig-Quilis M. Munell F, et al. Rev Neurol. 2018 Apr 1;66(7):241-250. Rev Neurol. 2018. PMID: 29557550 Free article. Review. English, Spanish.
Brainstem dysgenesis designates all those patients with congenital dysfunction of cranial nerves and muscle tone due to prenatal lesions or malformations of the brainstem. ...Due to phenotypic heterogeneity associated with brainstem dysgenesis, it is crucial to evaluate ea …
Brainstem dysgenesis designates all those patients with congenital dysfunction of cranial nerves and muscle tone due to prenatal lesi …
Congenital Brain Malformations: An Integrated Diagnostic Approach.
Chaudhari BP, Ho ML. Chaudhari BP, et al. Semin Pediatr Neurol. 2022 Jul;42:100973. doi: 10.1016/j.spen.2022.100973. Epub 2022 Apr 22. Semin Pediatr Neurol. 2022. PMID: 35868725 Review.
Congenital brain malformations are abnormalities present at birth that can result from developmental disruptions at various embryonic or fetal stages. ...An informed combination of imaging and genetic testing enables early and accurate diagnosis and ma …
Congenital brain malformations are abnormalities present at birth that can result from developmental disruptions at var …
Hyponatremia and hypernatremia in the newborn: in medio stat virtus.
Marcialis MA, Dessi A, Pintus MC, Marinelli V, Fanos V. Marcialis MA, et al. Front Biosci (Elite Ed). 2012 Jan 1;4(1):132-40. doi: 10.2741/e364. Front Biosci (Elite Ed). 2012. PMID: 22201859 Review.
Pathogenetic mechanisms and clinical timing of hypo-hypernatremia are well known in adult people whereas in the newborn is less clear how and when hypo-hypernatremia could alter cerebral osmotic equilibrium and after how long time brain cells adapt themselves …
Pathogenetic mechanisms and clinical timing of hypo-hypernatremia are well known in adult people whereas in the newborn is less clear …
Atelencephalic aprosencephaly.
Harris CP, Townsend JJ, Norman MG, White VA, Viskochil DH, Pysher TJ, Klatt EC. Harris CP, et al. J Child Neurol. 1994 Oct;9(4):412-6. doi: 10.1177/088307389400900416. J Child Neurol. 1994. PMID: 7822735
Embryologically, aprosencephaly is thought to occur after the optic vesicles form but before the cerebral vesicles appear. The syndrome is quite rare, with only 10 cases previously reported. ...The optic globes were completely formed and attached to hypoplastic optic nerve …
Embryologically, aprosencephaly is thought to occur after the optic vesicles form but before the cerebral vesicles appear. The syndro …
6,519 results