Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ulpu Seppänen"'
Autor:
Ulpu Seppänen, Tuija Lundán, Tuija Löppönen, Jarmo Körkkö, Jaakko Ignatius, Helena Kääriäinen
Publikováno v:
Arthritis Care & Research. 51:925-932
Objective To define the clinical, radiologic, and molecular genetic characteristics of a family with early progressive osteoarthritis mimicking childhood rheumatoid arthritis, Scheuermann-like changes of the spine, tall stature, short 3 and 4 metatar
Autor:
Renata Glazar, Ulpu Seppänen, Tim D. Spector, Liisa Carter, Malwina Czarny-Ratajczak, Anna Latos-Bielenska, Jaana Lohiniva, Jan Królewski, Leena Ala-Kokko, Kazimierz Kozlowski, Piotr Rogala, Merja Perälä, Lukasz Kolodziej
Publikováno v:
The American Journal of Human Genetics. 69:969-980
Multiple epiphyseal dysplasia (MED) is an autosomal dominantly inherited chondrodysplasia. It is clinically highly heterogeneous, partially because of its complex genetic background. Mutations in four genes, COL9A2, COL9A3, COMP, and MATR3, all codin
Autor:
Ulpu Seppänen, H. Olbing, O. Koskimies, I. Wikstad, Herbert Hirche, Hildegard Lax, Jean M. Smellie, Tytti Tamminen-Möbius
Publikováno v:
Radiology. 216:731-737
To determine whether medical or surgical treatment better promotes renal growth in children with severe vesicoureteric reflux (VUR) and to examine factors influencing renal growth.Three hundred two children younger than 11 years with urinary tract in
Autor:
Sirpa Kivirikko, Ulpu Seppänen, Petteri Paassilta, Outi Vierimaa, Leena Ala-Kokko, Jaana Lohiniva
Publikováno v:
American Journal of Medical Genetics. 90:216-222
We report on a three-generation family with multiple epiphyseal dysplasia (MED). The propositus had typical MED findings of knees, ankles, elbows, and hands in childhood. The 2 other affected relatives were adults. The main clinical findings consiste
Autor:
Jean M. Smellie, H. Olbing, Ulf Jodal, I. Wikstad, Ulpu Seppänen, Tytti Tamminen-Möbius, Ingemar Claesson
Publikováno v:
Pediatric Nephrology. 6:223-230
The renal findings on intravenous urography (IVU) are reported in 306 children (73 boys, 233 girls) from eight European centres entered into an international study comparing medical and surgical management of children with urinary tract infection and
Autor:
Tuija, Löppönen, Jarmo, Körkkö, Tuija, Lundan, Ulpu, Seppänen, Jaakko, Ignatius, Helena, Kääriäinen
Publikováno v:
Arthritis and rheumatism. 51(6)
To define the clinical, radiologic, and molecular genetic characteristics of a family with early progressive osteoarthritis mimicking childhood rheumatoid arthritis, Scheuermann-like changes of the spine, tall stature, short 3 and 4 metatarsals, and
Publikováno v:
Scandinavian journal of urology and nephrology. 24(3)
In order to detect possible urinary tract abnormalities among wetters, assessments of previous history completed by ultrasonography of the urinary tract and uroflowmetry were obtained for 145 wetting children and a random sample of 156 sex-matched no
Publikováno v:
Annual Review of Hydrocephalus ISBN: 9783662111543
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a432c47a1f0f2fdcac8e642211dd7ee5
https://doi.org/10.1007/978-3-662-11152-9_55
https://doi.org/10.1007/978-3-662-11152-9_55
Publikováno v:
Neuroradiology. 29:53-57
Assessment of hydrocephalus shunt dysfunction, especially when partial, causes severe differential diagnostic problems. Ordinary computer assisted tomography gives only indirect information about shunt dynamics and the estimation of intraventricular
Publikováno v:
Clinical radiology. 30(1)
Intravenous urography and voiding urethrocystography were performed on 255 children with urinary tract infection. Eighty-six (34%) of these children had some kind of abnormality of the urinary tract. Vesico-ureteral reflux was observed to 96 ureters