Výsledky vyhledávání - "C. B. van der Hagen"

A correlative study of prenatal ultrasound and post-mortem findings in fetuses and infants with an abnormal karyotype

Autor: C. B. Van Der Hagen, S. H. Torp, C. V. Isaksen, H.-G. Blaas, Eli Ormerod, Sturla H. Eik-Nes

Publikováno v: Ultrasound in Obstetrics and Gynecology. 16:37-45

Objective To compare ultrasound and post-mortem findings in 98 fetuses and infants with an abnormal karyotype. Design Criteria for inclusion were an ultrasound examination at the National Center for Fetal Medicine (NCFM), an abnormal karyotype, and a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e840e2a680a04b37c0ec1c6ebd5b0c0d
https://doi.org/10.1046/j.1469-0705.2000.00157.x

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Campomelic dysplasia — an underdiagnosed condition?

Autor: G. Stiris, J. C. Pedersen, C. B. van der Hagen, E. K. Normann

Publikováno v: European Journal of Pediatrics. 152:331-333

Campomelic dysplasia (CD) is a rare skeletal dysplasia. The incidence, reported in the literature, is 0.05-0.09 per 10,000 live births. During the period December 1985-December 1990 there were 18,350 live births with 4 cases of CD at Aker University

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::618932a42c49fe352a1a1a99f7592883
https://doi.org/10.1007/bf01956747

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Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study Group

Autor: T, Gedde-Dahl, O, Trygstad, L, Van Maldergem, J, Magré, C B, van der Hagen, B, Olaisen, M, Stenersen, B, Mevåg

Publikováno v: Acta paediatrica (Oslo, Norway : 1992). Supplement. 413

Five of the six families with the Berardinelli-Seip syndrome in Norway cluster in six adjacent rural municipalities of south-western Norway. The six patients from this area were born between 1951 and 1973, none between 1974 and 1995. The absence of n

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e0f3c242015ce414698b4a265a6d3fb5
https://pubmed.ncbi.nlm.nih.gov/8783773

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[Genetic disease in general practice. An interview study among general practitioners in Oppland and Oslo]

Autor: E, Hem, C B, van der Hagen, M H, Solaas

Publikováno v: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 114(9)

We interviewed 51 Norwegian general practitioners selected at random about their knowledge and practice of medical genetics. Of these doctors, 29 worked in Oslo and 22 in Oppland county. About 90% of the doctors working in Oslo knew where to refer pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cb4ece3814f3098878d4dc3fcb8ddeae
https://pubmed.ncbi.nlm.nih.gov/8009517

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[Karyotyping of fetuses with developmental disorders. A 5-year material 1985-89]

Autor: J M, Tuveng, S H, Eik-Nes, O, Sviggum, C, Isaksen, K, Berg, T P, Leren, C B, van der Hagen

Publikováno v: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 113(3)

During the period 1985 to 1989 foetal chromosomal analysis was performed in 121 of 318 pregnant women with foetal malformations detected by ultrasound. There were six failures. The percentage of foetuses karyotyped for developmental disorders increas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::82a4a16d15627090cb5676ce21d691cd
https://pubmed.ncbi.nlm.nih.gov/8441983

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Lethal Acute Gamma Radiation Accident at Kjeller, Norway: Report of a case

Autor: Brian Petersen, K. Kett, H. Høst, A. Brøgger, C. B. van der Hagen, T. Henriksen, J. Flatby, Per Stavem, F. Devik, P. S. Hoel

Publikováno v: Acta Radiologica: Oncology. 24:61-63

On September 2, 1982, a 64-year-old man accidently received a heavy dose of gamma radiation in a plant for sterilization by radiation. He developed an acute radiation syndrome. The leukocyte count rapidly diminished to low values, and extensive chrom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d8063b078025ef85a6327fed9ece92b
https://doi.org/10.3109/02841868509134366

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