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pro vyhledávání: '"Kurt Kaijser"'
Autor:
Kurt Kaijser
Publikováno v:
Clinical Genetics. 2:255-260
Autor:
Kurt Kaijser
Publikováno v:
Clinical Genetics. 5:254-258
The case described here is a non-mongoloid girl, with an extra, small, acrocentric chromosome. She shows some of the clinical features previously described in non-mongoloid children with a similar chromosomal karyotype, including severe mental retard
Autor:
Kurt Kaijser
Publikováno v:
Acta paediatrica. 32(3-4)
Summary. An investigation of the bacteriological diagnosis of throat tests made on 385 children aged from 1 month to 13 years who have been treated at the Crown Princess Louise's Children's Hospital (Kronprinsessan Lovisas Barnsjukhus) in Stockholm f
Autor:
Kurt Kaijser
Publikováno v:
Acta Paediatrica. 27:245-272
Autor:
Kurt Kaijser, Fredrik Fränkel
Publikováno v:
Acta Paediatrica. 38:340-350
Summary An investigation of the distribution of the birth weights per month in a material comprising 8 284 children born during a 10 year period in the Maternity Department of a General Hospital in a northerly part of Sweden (latitude 64) is reported
Autor:
Kurt Kaijser
Publikováno v:
Acta Endocrinologica. 3:351-364
Publikováno v:
Acta Paediatrica. 56:279-285
Serum specimens from 161 pregnant women or newborn children and from 280 females of different age groups, obtained in the cities of Stockholm and Eskilstuna, Sweden, were tested for neutralizing antibody to rubella virus, some of them also for hemagg
Autor:
Kurt Kaijser
Publikováno v:
Acta Paediatrica. 25:149-155
Summary. A boy, three years old, healthy and well-developed, who was by chance X-ray-examined, showed a typical interposition of the colon between the right part of the diaphragm and the liver. At a new X-ray-examination with a barium-enema 3 days la
Publikováno v:
Acta paediatrica. 46(2)
Autor:
Kurt Kaijser
Publikováno v:
The Lancet. 278:1362