Biomedical subjects
E O Nightingale
Publications and source records attributed to E O Nightingale.
Immigrating unaccompanied minors--a neglected minority?
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Promoting the healthy development of adolescents.
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Children and childhoods. Hidden casualties of war and civil unrest.
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Physicians and the basic human rights of women.
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Partnerships for improving border health.
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Last-minute ban on medical visit to South Africa.
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Visas not approved for medical delegation to South Africa.
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Facilitating the transitions of adolescence. Council on Adolescent Development.
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Conjunction of biomedical and behavioral sciences: can research on alcoholism show the way?
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The medical profession and the prevention of torture.
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Support urged for Syrian doctors.
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Science for health in the future.
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Research opportunities in alcoholism.
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Toward a sane national policy on food safety.
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Recommendations for a national policy on poliomyelitis vaccination.
Declining numbers of adequately vaccinated persons, new data about the comparative safety and effectiveness of live, attenuated and killed poliomyelitis-virus vaccines, increased consumer awareness of adverse reactions and pressure from manufacturers seeking protection from liability were factors leading the Institute of Medicine to re-examine poliomyelitis vaccination programs. The relative merits of live and killed virus vaccines as immunizing agents were reviewed within the context of the 60 to 70 per cent level of poliomyelitis vaccination now reached in the United States. Until about 90 per cent of persons are adequately immunized, the continued use of live-virus vaccines for infants is recommended, with provision that certain categories of persons receive killed-virus vaccine. Vaccination with attenuated live virus of children 11 to 12 years old is suggested to reduce vaccine-associated disease when they become parents of vaccinated infants. Recommendations are made on education, research, liability and informed consent as they pertain to prevention of polyomyelitis.
Observations on patients with neural-tube defects in a metropolitan hospital clinic: an epidemiological history.
A survey of the population of the Spina Bifida Service (107 patients) of Georgetown University Hospital, Washington, D.C., and of a control population in the same hospital revealed that, although situated in an ethnically heterogeneous area, Service patients with a history of neural-tube defects in siblings or family significantly more often had ancestors on both sides from the British Isles than did either isolated cases or the controls. In addition, of 107 families reviewed, nine had more than one affected child, nine had a positive family history for neural-tube defects, and nine of the patients and seven of an estimated total of 220 siblings had an unrelated major birth-defect. These incidences are among the highest published so far. Contrary to other surveys, there was no deficiency of twinning among the sibships, nor of males among the Spina Bifida Service patients. These observations indicate the desirability of studying each population of patients with neural-tube defects in order to provide more realistic counseling and so that clues may be gathered as to the genetic mechanisms and environmental factors which led to the production of such defects.