Sökning: "scoliosis"

Visar resultat 26 - 30 av 30 avhandlingar innehållade ordet scoliosis.

  1. 26. Range Camera Imaging : From Human Body Measurements to Very Large 3D Points Scenes Visualization

    Författare :Gaël Neuez; Chalmers tekniska högskola; []
    Nyckelord :TEKNIK OCH TEKNOLOGIER; ENGINEERING AND TECHNOLOGY; 3D visualization; EASYTEX; anatomical landmarks; body scanner; range camera; 2D image projections; structured light; octree data structure;

    Sammanfattning : The use of camera range imaging for the purpose of 3-dimensional representation and non-contact measures is widely used in industry, medicine, computer-aided design and other areas. Different range imaging methods can be applied, such as stereo, laser sheet of light, and structured light. LÄS MER

  3. 27. Congenital muscular dystrophy with laminin α2 chain-deficiency. Initiation of disease and development of treatment

    Författare :Zandra Körner; Muskelbiologi; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; muskeldystrofi; Muscular dystrophy; Autophagy; proteasome; Laminin; MDC1A;

    Sammanfattning : Congenital muscle dystrophy type 1A (MDC1A) is a muscle disease caused bymutations in the LAMA2 gene, encoding the basement membrane protein lamininα2 chain. MDC1A patients exhibit neonatal onset of muscle weakness, progressivemuscle wasting and hypotonia, joint contractures that mostly affect elbows, hips,knees and ankles along with scoliosis and delayed motor milestones. LÄS MER

  4. 28. Living with osteogenesis imperfecta

    Författare :Veronica Balkefors; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Osteogenesis Imperfecta (OI) is a hereditary connective tissue disorder with fragility of the bones as the dominant symptom. There is no cure for OI, but symptoms are treated with medical, orthopaedic and physiotherapy methods. The disease group is very heterogeneous and knowledge about adults living with the milder forms, type I or IV is limited. LÄS MER

  5. 29. Application of next generation sequencing in genetic and genomic studies

    Författare :Jingwen Wang; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Genetic variants that spread along the human genome play vital roles in determining our traits, affecting development and potentially causing disorders. Most common disorders have complex underlying mechanisms involving genetic or environmental factors and the interaction between them. LÄS MER

  7. 30. Long-term follow-up in children born with congenital diaphragmatic hernia

    Författare :Elin Öst; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Congenital diaphragmatic hernia (CDH) is a developmental defect which occurs in approximately 1 per 3000 births. The incomplete development of the diaphragm early in gestation allows abdominal viscera to herniate into the thoracic cavity. The malformation differs in size and can occur on either one or both sides, but most commonly on the left. LÄS MER