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- Lundqvist, Anette, et al.
(författare)
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8 av 10 barnmorskor gav information om folsyra : de flesta ansåg sig ha otillräckliga kunskaper
- 2004
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Ingår i: Läkartidningen. - Stockholm : Sveriges läkarförbund. - 0023-7205 .- 1652-7518. ; 101:15-16, s. 1380-1386
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Deficiency of folic acid increases the risk for neural tube defects among newborn children and megaloblastic anaemia in the mother. The aim of this study was to make a survey of how midwives working in maternity health care, family planning guidance, and specialist prenatal care in a Swedish county inform women of childbearing age about folic acid. The questionnaire study showed that 79% of the midwives informed the women about folic acid. Usually, the women received information first when they asked for it and midwifes were less prone to inform young women about folic acid. 87% of the midwives felt that they did not know enough about folic acid. Conclusions: Midwives play an important role in information about the need of folic acid intake for women in childbearing age. Changes in local routines, guidelines and further education of midwifes would subsequently provide information about the importance of folic acid to women in childbearing age.
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- Sandström, Herbert, et al.
(författare)
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[Localized gene of the rare "Norrland disease". CDA-III blood disease with dominant heredity].
- 1999
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Ingår i: Läkartidningen. - 0023-7205 .- 1652-7518. ; 96:4, s. 343-7
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Tidskriftsartikel (refereegranskat)abstract
- The article consists in a review of available knowledge of the rare blood disorder, congenital dyserythropoietic anaemia, type III (CDA-III), a disease characterised by autosomal dominant heredity, and mild to moderate haemolytic anaemia. The gene causing CDA-III has been localised on chromosome 15q22. Most patients are adapted to their disease, and have few or no overt manifestations. Bone marrow examination yields a characteristic picture of erythroid hyperplasia and multinucleate erythroblasts. A Swedish family affected with CDA-III has been reported to be characterised by a high prevalence of monoclonal gammopathy and angioid streaks, a triad suggested by the authors to represent a hitherto unreported syndrome.
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