Search Results - "Harjama, L."

  • Showing 1 - 6 results of 6
Refine Results
  1. 1

    A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma by Brandt, E., Harjama, L., Elomaa, O., Saarela, J., Donner, K., Lappalainen, K., Kivirikko, S., Ranki, A., Kere, J., Kettunen, K., Hannula‐Jouppi, K.

    “…Background Hereditary palmoplantar keratodermas (hPPKs) comprise a heterogeneous group of skin disorders characterized by persistent palmoplantar…”
    Get full text
    Journal Article
  2. 2
  3. 3

    Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients by Harjama, L., Karvonen, V., Kettunen, K., Elomaa, O., Einarsdottir, E., Heikkilä, H., Kivirikko, S., Ellonen, P., Saarela, J., Ranki, A., Kere, J., Hannula‐Jouppi, K.

    “…Background Hereditary palmoplantar keratodermas (PPK) represent a heterogeneous group of rare skin disorders with epidermal hyperkeratosis of the palms and…”
    Get full text
    Journal Article
  4. 4

    A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign by Karvonen, V., Harjama, L., Heliö, K., Kettunen, K., Elomaa, O., Koskenvuo, J.W., Kere, J., Weckström, S., Holmström, M., Saarela, J., Ranki, A., Heliö, T., Hannula‐Jouppi, K.

    “…Background PPKs represent a heterogeneous group of disorders with hyperkeratosis of palmar and/or plantar skin. PPK, hair shaft abnormalities, cardiomyopathy…”
    Get full text
    Journal Article
  5. 5
  6. 6