Congenital pseudarthrosis of the tibia: Treatment and outcome at skeletal maturity in 10 children von Heikkinen, Erkki S, Poyhonen, Minna H, Kinnunen, Pentti K, Seppänen, Ulpu I

Volltext

A Mutation in COL9A1 Causes Multiple Epiphyseal Dysplasia: Further Evidence for Locus Heterogeneity von Czarny-Ratajczak, Malwina, Lohiniva, Jaana, Rogala, Piotr, Kozlowski, Kazimierz, Perälä, Merja, Carter, Liisa, Spector, Tim D., Kolodziej, Lukasz, Seppänen, Ulpu, Glazar, Renata, Królewski, Jan, Latos-Bielenska, Anna, Ala-Kokko, Leena

Volltext

Matrix Metalloproteinase-21 Expression Is Associated with Keratinocyte Differentiation and Upregulated by Retinoic Acid in HaCaT Cells von Skoog, Tiina, Elomaa, Outi, Pasonen-Seppänen, Sanna M., Forsberg, Sofi, Ahokas, Katja, Jeskanen, Leila, Pärssinen, Jenita, Tiala, Inkeri, Rollman, Ola, Lohi, Jouko, Saarialho-Kere, Ulpu

Volltext

Five-year study of medical or surgical treatment in children with severe reflux : radiological renal findings. The international reflux study in children von SMELLIE, J. M, TAMMINEN-MÖBIUS, T, OLBING, H, CLAESSON, I, WIKSTAD, I, JODAL, U, SEPPANEN, U

Volltext

Childhood‐onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg 75 ‐Cys mutation in procollagen type II gene (COL2A1) von Löppönen, Tuija, Körkkö, Jarmo, Lundan, Tuija, Seppänen, Ulpu, Ignatius, Jaakko, Kääriäinen, Helena

Volltext

Childhood-onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75-Cys mutation in procollagen type II gene (COL2A1) von LÖPPÖNEN, Tuija, KÖRKKÖ, Jarmo, LUNDAN, Tuija, SEPPÄNEN, Ulpu, IGNATIUS, Jaakko, KÄÄRIÄINEN, Helena

Volltext

Screening of urinary tract abnormalities among day and nightwetting children von J rvelin, Marjo R., Huttunen, Niilo-Pekka, Sepp nen, Juhani, Sepp nen, Ulpu, Moilanen, Irma

Volltext

Splicing mutations in the COL3 domain of collagen IX cause multiple epiphyseal dysplasia von Lohiniva, Jaana, Paassilta, Petteri, Seppänen, Ulpu, Vierimaa, Outi, Kivirikko, Sirpa, Ala-Kokko, Leena

Volltext

Screening of Urinary Tract Abnormalities Among Day and Nightwetting Children von Järvelin, Marjo R., Huttunen, Niilo-Pekka, Seppänen, Juhani, Seppänen, Ulpu, Moilanen, Irma

Volltext

Childhood‐onset osteoarthritis, tall stature, and sensorineural hearing loss associated with Arg75‐Cys mutation in procollagen type II gene (COL2A1) von Löppönen, Tuija, Körkkö, Jarmo, Lundan, Tuija, Seppänen, Ulpu, Ignatius, Jaakko, Kääriäinen, Helena

Volltext

A lethal autosomal recessive syndrome of multiple congenital contractures von Herva, Riitta, Leisti, Jaakko, Kirkinen, Pertti, Seppänen, Ulpu, Opitz, John M., Reynolds, James F.

Volltext

Prediction of vesico-ureteral reflux in children from intravenous urography films von Lanning, Peter, Seppänen, Ulpu, Huttunen, Niilo-Pekka, Uhari, Matti

Volltext