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

Year Number of Results
1947 1
1948 1
1949 1
1952 1
1954 1
1957 1
1958 2
1959 1
1960 1
1961 1
1962 2
1963 4
1964 1
1965 4
1966 5
1967 9
1968 4
1969 5
1970 3
1971 8
1972 7
1973 4
1974 13
1975 75
1976 82
1977 86
1978 88
1979 81
1980 104
1981 125
1982 103
1983 118
1984 168
1985 190
1986 162
1987 191
1988 196
1989 194
1990 237
1991 242
1992 279
1993 292
1994 311
1995 349
1996 365
1997 392
1998 425
1999 448
2000 453
2001 438
2002 501
2003 491
2004 528
2005 598
2006 600
2007 660
2008 735
2009 715
2010 781
2011 845
2012 877
2013 1027
2014 973
2015 944
2016 974
2017 976
2018 965
2019 1032
2020 1214
2021 1225
2022 1089
2023 934
2024 468

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22,691 results

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Quoted phrase not found in phrase index: "Hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome"
Page 1
Histopathology of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis.
Takahashi Y, Fukusato T. Takahashi Y, et al. World J Gastroenterol. 2014 Nov 14;20(42):15539-48. doi: 10.3748/wjg.v20.i42.15539. World J Gastroenterol. 2014. PMID: 25400438 Free PMC article. Review.
Nonalcoholic fatty liver disease (NAFLD), a hepatic manifestation of metabolic syndrome, is the most common chronic liver disease, and the prevalence is rapidly increasing worldwide. ...Steatosis, lobular inflammation, and hepatocellular ballooning are all necessary compon …
Nonalcoholic fatty liver disease (NAFLD), a hepatic manifestation of metabolic syndrome, is the most common chronic liver disease, an …
Use of HINTS in the acute vestibular syndrome. An Overview.
Kattah JC. Kattah JC. Stroke Vasc Neurol. 2018 Jun 23;3(4):190-196. doi: 10.1136/svn-2018-000160. eCollection 2018 Dec. Stroke Vasc Neurol. 2018. PMID: 30637123 Free PMC article. Review.
Following the initial description of HINTS to diagnose acute vestibular syndrome (AVS) in 2009, there has been significant interest in the systematic evaluation of HINTs to diagnose stroke and other less common central causes of AVS. ...Twenty-five papers provide a summary …
Following the initial description of HINTS to diagnose acute vestibular syndrome (AVS) in 2009, there has been significant interest i …
Molecular Mechanisms Involved in Craniosynostosis.
Yapijakis C, Pachis N, Sotiriadou T, Vaila C, Michopoulou V, Vassiliou S. Yapijakis C, et al. In Vivo. 2023 Jan-Feb;37(1):36-46. doi: 10.21873/invivo.13052. In Vivo. 2023. PMID: 36593018 Free PMC article. Review.
Craniosynostosis refers to the early fusion of one or many cranial sutures, causing craniofacial abnormalities observed in 1:2,500 births worldwide. In most cases (85%), craniosynostosis is presented as sporadic anomaly (non-syndromic craniosynostosis) …
Craniosynostosis refers to the early fusion of one or many cranial sutures, causing craniofacial abnormalities observed in 1:2 …
Human dendritic cell immunodeficiencies.
Bigley V, Cytlak U, Collin M. Bigley V, et al. Semin Cell Dev Biol. 2019 Feb;86:50-61. doi: 10.1016/j.semcdb.2018.02.020. Epub 2018 Feb 23. Semin Cell Dev Biol. 2019. PMID: 29452225 Review.
This forms the basis of predicting the effects of DC deficiency in vivo and understanding the consequences of specific mutations on DC development and function. DC deficiency syndromes are associated with heterozygous GATA2 mutation, bi-allelic and heterozygous IRF8 …
This forms the basis of predicting the effects of DC deficiency in vivo and understanding the consequences of specific mutations on D …
Etiologies of uterine malformations.
Jacquinet A, Millar D, Lehman A. Jacquinet A, et al. Am J Med Genet A. 2016 Aug;170(8):2141-72. doi: 10.1002/ajmg.a.37775. Epub 2016 Jun 8. Am J Med Genet A. 2016. PMID: 27273803 Review.
Although most occurrences ostensibly seem sporadic, familial recurrences have been observed, which strongly implicate genetic factors. Through the study of animal models, human syndromes, and structural chromosomal variation, several candidate genes have been propos …
Although most occurrences ostensibly seem sporadic, familial recurrences have been observed, which strongly implicate genetic factors …
Combined and complex vascular malformations.
Clemens RK, Pfammatter T, Meier TO, Alomari AI, Amann-Vesti BR. Clemens RK, et al. Vasa. 2015 Mar;44(2):92-105. doi: 10.1024/0301-1526/a000414. Vasa. 2015. PMID: 25698387 Review.
This is especially the case in combined or complex vascular malformations or vascular malformations that are part of syndromes as these have overlapping clinical and imaging features. New entities in the field of vascular anomalies have been described recently like …
This is especially the case in combined or complex vascular malformations or vascular malformations that are part of syndromes as the …
The telecanthus-hypospadias syndrome.
Stevens CA, Wilroy RS Jr. Stevens CA, et al. J Med Genet. 1988 Aug;25(8):536-42. doi: 10.1136/jmg.25.8.536. J Med Genet. 1988. PMID: 3050099 Free PMC article. Review.
In our series, the most frequent anomalies include telecanthus 18/18, hypospadias 18/18, cleft lip/palate or uvula 8/18, high, broad nasal bridge 10/11, cranial abnormality 12/18, congenital heart defect 3/18, upper urinary tract anomaly 4/9, and mental retardation …
In our series, the most frequent anomalies include telecanthus 18/18, hypospadias 18/18, cleft lip/palate or uvula 8/18, high, broad …
Genetics of patella hypoplasia/agenesis.
Vanlerberghe C, Boutry N, Petit F. Vanlerberghe C, et al. Clin Genet. 2018 Jul;94(1):43-53. doi: 10.1111/cge.13209. Epub 2018 Apr 11. Clin Genet. 2018. PMID: 29322497 Review.
When absent or hypoplastic, recurrent knee subluxations, patellofemoral dysfunction and early gonarthrosis may occur. Patella hypoplasia/agenesis may be isolated or observed in syndromic conditions, either as the main clinical feature (Nail-patella syndrome, …
When absent or hypoplastic, recurrent knee subluxations, patellofemoral dysfunction and early gonarthrosis may occur. Patella hypoplasia/age …
Acrofacial dysostoses.
Le Merrer M, Cikuli M, Ribier J, Briard ML. Le Merrer M, et al. Am J Med Genet. 1989 Jul;33(3):318-22. doi: 10.1002/ajmg.1320330307. Am J Med Genet. 1989. PMID: 2801764
She also has downward-slanting palpebral fissures, malar hypoplasia, and deepset eyes. This observation offers an opportunity to revisit the acrofacial dysostoses syndromes, including Nager-Reynier syndrome, Genee-Wiedeman syndrome, and lethal forms... …
She also has downward-slanting palpebral fissures, malar hypoplasia, and deepset eyes. This observation offers an opportunity to revi …
Survival Trends and Syndromic Esophageal Atresia.
Tan Tanny SP, Beck C, King SK, Hawley A, Brooks JA, McLeod E, Hutson JM, Teague WJ. Tan Tanny SP, et al. Pediatrics. 2021 May;147(5):e2020029884. doi: 10.1542/peds.2020-029884. Pediatrics. 2021. PMID: 33911029
BACKGROUND AND OBJECTIVES: Presence of a syndrome (or association) is predictive of poor survival in esophageal atresia (EA). ...Data were collected for recognized risk factors: preterm delivery; birth weight <1500 g; major cardiac disease; vertebral defects, ana …
BACKGROUND AND OBJECTIVES: Presence of a syndrome (or association) is predictive of poor survival in esophageal atresia (EA). …
22,691 results
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