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

Year Number of Results
1945 2
1946 1
1947 3
1948 1
1950 2
1952 1
1953 2
1954 6
1955 2
1956 4
1957 3
1958 5
1959 3
1960 5
1961 7
1962 6
1963 16
1964 33
1965 22
1966 11
1967 26
1968 23
1969 34
1970 51
1971 67
1972 101
1973 127
1974 161
1975 269
1976 278
1977 295
1978 268
1979 300
1980 291
1981 308
1982 303
1983 357
1984 510
1985 540
1986 531
1987 581
1988 737
1989 860
1990 1068
1991 1064
1992 1148
1993 1306
1994 1490
1995 1646
1996 1715
1997 1841
1998 1929
1999 2005
2000 2026
2001 2111
2002 2343
2003 2644
2004 2721
2005 3335
2006 3317
2007 3641
2008 3723
2009 3870
2010 4138
2011 4500
2012 4818
2013 5327
2014 5525
2015 5757
2016 5770
2017 6056
2018 6105
2019 6429
2020 8439
2021 8982
2022 6923
2023 5956
2024 2477

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123,882 results

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Quoted phrase not found in phrase index: "Microcephaly-seizures-intellectual disability-heart disease syndrome"
Page 1
VEXAS Syndrome-A Review of Pathophysiology, Presentation, and Prognosis.
Koster MJ, Samec MJ, Warrington KJ. Koster MJ, et al. J Clin Rheumatol. 2023 Sep 1;29(6):298-306. doi: 10.1097/RHU.0000000000001905. Epub 2022 Oct 17. J Clin Rheumatol. 2023. PMID: 36251488 Review.
VEXAS ( V acuoles, E 1 enzyme, X -linked, A utoinflammatory, S omatic) syndrome is a newly identified disease caused by somatic mutations in the UBA1 gene resulting in refractory autoinflammatory features, frequently accompanied by cytopenias. ...The pathophysiology …
VEXAS ( V acuoles, E 1 enzyme, X -linked, A utoinflammatory, S omatic) syndrome is a newly identified disease caused by somati …
Axillary web syndrome: Incidence, pathogenesis, and management.
Dinas K, Kalder M, Zepiridis L, Mavromatidis G, Pratilas G. Dinas K, et al. Curr Probl Cancer. 2019 Dec;43(6):100470. doi: 10.1016/j.currproblcancer.2019.02.002. Epub 2019 Mar 15. Curr Probl Cancer. 2019. PMID: 30898366 Review.
Axillary web syndrome (AWS) refers to the development of fibrotic bands or "cords" in the axilla of patients who have undergone axillary lymph node dissection for breast cancer. ...
Axillary web syndrome (AWS) refers to the development of fibrotic bands or "cords" in the axilla of patients who have undergone axill …
Aspiration syndromes and associated lung injury: incidence, pathophysiology and management.
Košutova P, Mikolka P. Košutova P, et al. Physiol Res. 2021 Dec 30;70(Suppl4):S567-S583. doi: 10.33549/physiolres.934767. Physiol Res. 2021. PMID: 35199544 Free PMC article. Review.
Aspiration is a common condition affecting healthy or sick patients which could create an acute or chronic inflammatory reaction in the lungs. Aspiration syndromes could be categorized according to a content entering the respiratory system into bacterial aspiration pneumon …
Aspiration is a common condition affecting healthy or sick patients which could create an acute or chronic inflammatory reaction in the lung …
Alstrom syndrome.
Marshall JD, Beck S, Maffei P, Naggert JK. Marshall JD, et al. Eur J Hum Genet. 2007 Dec;15(12):1193-202. doi: 10.1038/sj.ejhg.5201933. Epub 2007 Oct 17. Eur J Hum Genet. 2007. PMID: 17940554
Very high incidences of additional disease phenotypes that may severely affect prognosis and survival include endocrine abnormalities, dilated cardiomyopathy, pulmonary fibrosis and restrictive lung disease, and progressive hepatic and renal failure. ...Most …
Very high incidences of additional disease phenotypes that may severely affect prognosis and survival include endocrine abnorm …
ROSAH syndrome mimicking chronic uveitis.
Fardeau C, Alafaleq M, Dhaenens CM, Dollfus H, Koné-Paut I, Grunewald O, Morel JB, Titah C, Saadoun D, Lazeran PO, Meunier I. Fardeau C, et al. Clin Genet. 2023 Apr;103(4):453-458. doi: 10.1111/cge.14286. Epub 2022 Dec 30. Clin Genet. 2023. PMID: 36543582
To suggest a unique missense variant candidate based on long-term ophthalmological changes and associated systemic signs described in five patients from two unrelated families affected by an autosomal dominant multi-systemic disorder including Retinal dystrophy, Optic nerve oedem …
To suggest a unique missense variant candidate based on long-term ophthalmological changes and associated systemic signs described in five p …
When should clinicians use the term syndrome?
Nugent K, Nugent R, Yang S. Nugent K, et al. Am J Med Sci. 2023 Jun;365(6):475-479. doi: 10.1016/j.amjms.2023.03.001. Epub 2023 Mar 9. Am J Med Sci. 2023. PMID: 36906228 Review.
In particular, the word syndrome should imply a definite and stable association between patient characteristics that have implications for treatment, prognosis, pathogenesis, and possibly clinical studies. ...Clinicians should use the word syndrome carefully. …
In particular, the word syndrome should imply a definite and stable association between patient characteristics that have implication …
Coronavirus Disease: Subacute to Chronic Neuroimaging Findings.
Mogensen MA, Filippi CG. Mogensen MA, et al. Neuroimaging Clin N Am. 2023 Feb;33(1):69-82. doi: 10.1016/j.nic.2022.07.004. Epub 2022 Jul 18. Neuroimaging Clin N Am. 2023. PMID: 36404048 Free PMC article. Review.
Several neurologic disorders are associated with coronavirus disease 2019 (COVID-19). In this article, clinical syndromes typically occurring in the subacute to chronic phase of illness and their neuroimaging findings are described with discussion of their COVID-19 …
Several neurologic disorders are associated with coronavirus disease 2019 (COVID-19). In this article, clinical syndromes typi …
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
Calcagni G, Unolt M, Digilio MC, Baban A, Versacci P, Tartaglia M, Baldini A, Marino B. Calcagni G, et al. Expert Rev Mol Diagn. 2017 Sep;17(9):861-870. doi: 10.1080/14737159.2017.1360766. Epub 2017 Aug 3. Expert Rev Mol Diagn. 2017. PMID: 28745539 Review.
Advances in genetics allowed a better definition of the role of specific genetic background in the etiology of syndromic congenital heart defects (CHDs). The identification of a number of disease genes responsible for different syndromes have led to the ident …
Advances in genetics allowed a better definition of the role of specific genetic background in the etiology of syndromic congenital h …
Muir-Torre syndrome.
Ponti G, Ponz de Leon M. Ponti G, et al. Lancet Oncol. 2005 Dec;6(12):980-7. doi: 10.1016/S1470-2045(05)70465-4. Lancet Oncol. 2005. PMID: 16321766 Review.
Muir-Torre syndrome is an autosomal-dominant skin condition of genetic origin, characterised by tumours of the sebaceous gland or keratoacanthoma that are associated with visceral malignant diseases. The cutaneous characteristics of Muir-Torre syndrome are se …
Muir-Torre syndrome is an autosomal-dominant skin condition of genetic origin, characterised by tumours of the sebaceous gland or ker …
Toxic anterior segment syndrome-an updated review.
Park CY, Lee JK, Chuck RS. Park CY, et al. BMC Ophthalmol. 2018 Oct 25;18(1):276. doi: 10.1186/s12886-018-0939-3. BMC Ophthalmol. 2018. PMID: 30359246 Free PMC article. Review.
BACKGROUND: Toxic anterior segment syndrome (TASS) can be a rare complication of anterior segment surgery. ...METHODS: English articles related to TASS were retrieved from "PubMed" using the following keywords; "toxic anterior segment syndrome" or "TASS". The author …
BACKGROUND: Toxic anterior segment syndrome (TASS) can be a rare complication of anterior segment surgery. ...METHODS: English articl …
123,882 results
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