The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
Long term outcome in children of sex chromosome abnormalities
Open accessAbstract
We tested whether the effect of influenza activity on invasive pneumococcal disease incidence and severity varies between age and comorbidity groups. Weekly rates of invasive pneumococcal disease were obtained from the Danish National Laboratory Surveillance System (1977–2007). Influenza-like illness data were collected from a sentinel surveillance system at the Statens Serum Institut (Copenhagen, Denmark). We fitted Poisson regression models for invasive pneumococcal disease, with predictors of seasonality, trends and influenza activity, and allowed the influenza activity variable to vary by comorbidity level and clinical presentation. Influenza activity accounted for 8.4% (95% CI 4.8−11.9%) and 6.9% (95% CI 5.4–10.2%) of all invasive pneumococcal disease cases among those aged 15–39 and ≥40 years, respectively, but had no measurable impact among children aged <15 years. Influenza activity was associated with significant increases in the incidence of invasive pneumococcal pneumonia in both children and adults. The association was more pronounced among younger adults without comorbidities. Case fatality also varied seasonally among the elderly, and this variation might be associated with influenza activity. Pneumococcal incidence and the severity of disease varied seasonally and between age groups. The effect of influenza activity on pneumococcal disease varied between children and adults, and this difference was largely due to differences in disease presentation.
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Cites
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Self-citationHarmon, R. J., Bender, B. G., Linden, M. G., & Robinson, A. (1998) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/00004583-199803000-00013 · Cited by 118
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Cited by
Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study
Bojesen, A., Juul, S., & Gravholt, C. H. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2002-021491 · Cited by 894
Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism
On behalf of the Klinefelter ItaliaN Group (KING), Bonomi, M., Rochira, V., Pasquali, D., Balercia, G., Jannini, E. A., & Ferlin, A. (2017) · Journal of Endocrinological Investigation · doi:10.1007/s40618-016-0541-6 · Cited by 365
Klinefelter Syndrome: Integrating Genetics, Neuropsychology, and Endocrinology
Gravholt, C. H., Chang, S., Wallentin, M., Fedder, J., Moore, P., & Skakkebæk, A. (2018) · Endocrine Reviews · doi:10.1210/er.2017-00212 · Cited by 328
Ottesen, A. M., Aksglaede, L., Garn, I., Tartaglia, N., Tassone, F., Gravholt, C. H., Bojesen, A., Sørensen, K., Jørgensen, N., Rajpert‐De Meyts, E., et al. (2010) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.33334 · Cited by 219
Behavioral and Social Phenotypes in Boys With 47,XYY Syndrome or 47,XXY Klinefelter Syndrome
Ross, J. L., Roeltgen, D. P., Kushner, H., Zinn, A. R., Reiss, A., Bardsley, M. Z., McCauley, E., & Tartaglia, N. (2012) · Pediatrics · doi:10.1542/peds.2011-0719 · Cited by 185
Metadata
- Authors
- Ratcliffe, S.
- Venue
- Archives of Disease in Childhood
- Publisher
- BMJ
- Published
- 1999-02-01
- Volume
- 80
- Issue
- 2
- Pages
- 192-195
- ISSN
- 0003-9888 (ISSN-L)
- 1468-2044
- OpenAlex
- W2141872203
- Cited by
- 334
- References
- 21
- FWCI
- 3.83
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Ratcliffe, S. (1999). Long term outcome in children of sex chromosome abnormalities. Archives of Disease in Childhood. https://doi.org/10.1136/adc.80.2.192
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.