Search Results - "Hagelsteen, J"

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  1. 1

    Bowel and bladder control of children with myelomeningocele: a Nordic study by Lie, H R, Lagergren, J, Rasmussen, F, Lagerkvist, B, Hagelsteen, J, Börjeson, M C, Muttilainen, M, Taudorf, K

    Published in Developmental medicine and child neurology (01-12-1991)
    “…The urinary and bowel control was studied of 527 children with myelomeningocele aged between four and 18 years. Information was obtained from medical records…”
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  2. 2

    Children with myelomeningocele: the impact of disability on family dynamics and social conditions. A Nordic study by Lie, H R, Börjeson, M C, Lagerkvist, B, Rasmussen, F, Hagelsteen, J H, Lagergren, J

    Published in Developmental medicine and child neurology (01-11-1994)
    “…Family dynamics and social conditions were studied of 527 children with myelomeningocele aged four to 18 years from Denmark, Finland, Norway and Sweden; the…”
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  3. 3

    Disability in children with myelomeningocele. A Nordic study by Hagelsteen, J H, Lagergren, J, Lie, H R, Rasmussen, F, Børjeson, M C, Lagerkvist, B, Muttilainen, M, Taudorf, K, Køhler, L

    Published in Acta pædiatrica Scandinavica (01-09-1989)
    “…This study was carried out to evaluate the medical impairments and disability among 527 children with myelomeningocele living in four Nordic countries. The…”
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  4. 4

    Nordic children with myelomeningocele. Parents' assessments of the handicap and physicians' classifications of the disabilities by Rasmussen, F, Lie, H R, Hagelsteen, J H, Lagergren, J, Börjeson, M C, Lagerkvist, B, Köhler, L

    Published in Acta pædiatrica (Oslo) (01-03-1993)
    “…The differences between parents' assessments of their child's handicap and professionals' assessment of disabilities were studied in 486 Nordic children with…”
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  5. 5

    Instability of lymphocyte chromosomes in a girl with Rothmund-Thomson syndrome by Orstavik, K H, McFadden, N, Hagelsteen, J, Ormerod, E, van der Hagen, C B

    Published in Journal of medical genetics (01-07-1994)
    “…Rothmund-Thomson syndrome is a rare autosomal recessive syndrome characterised by poikiloderma of the face and extremities, alopecia, short stature, and…”
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  6. 6

    Prosopagnosia. A rare disorder of visual perception by Wolland, A M, Hagelsteen, J H

    Published in Tidsskrift for den Norske Lægeforening (30-11-1991)
    “…Prosopagnosia is a rare neurological sign, characterized by disturbance of recognition of faces. It is important to remember that prosopagnosia can appear as a…”
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  7. 7
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    Nordic children with myelomeningocele: the utilization of and satisfaction with health care and medical services by Lie, H R, Lagerkvist, B, Rasmussen, F, Hagelsteen, J, Borjeson, M C, Lagergren, J, Kohler, L

    Published in Scandinavian journal of social medicine (01-12-1995)
    “…A study was conducted on utilization of and satisfaction with the health care and medical services among 527 Scandinavian children (aged 4-18) with…”
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  9. 9
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