Zobrazeno 1 - 10
of 56
pro vyhledávání: '"U. Seppänen"'
Autor:
U. Seppänen, K.-D. Ebel, I. Wikstad, J. M. Smellie, Tytti Tamminen-Möbius, H. Olbing, I. Claesson
Publikováno v:
Journal of Urology. 148:1653-1656
A total of 321 children less than 11 years old with nonobstructive grade III or IV vesicoureteral reflux and with previous urinary tract infection was randomly allocated to medical or surgical treatment in the European branch of the International Ref
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::002296a42d860ea9a5caf03db83b09f8
https://doi.org/10.1016/s0022-5347(17)36995-1
https://doi.org/10.1016/s0022-5347(17)36995-1
Autor:
R. Sixt, H. Olbing, U. Seppänen, K.-D. Ebel, E. Brunier, Tytti Tamminen-Möbius, Robert L. Lebowitz
Publikováno v:
Journal of Urology. 148:1662-1666
A total of 401 children with severe vesicoureteral reflux (97 with grade III and 304 with grade IV) was entered into the European branch of the International Reflux Study in Children. Of these patients 37 with grade III and 43 with grade IV reflux we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8852e0ac44d3d376063afa559deb7ce
https://doi.org/10.1016/s0022-5347(17)36997-5
https://doi.org/10.1016/s0022-5347(17)36997-5
Publikováno v:
American journal of medical genetics. 90(3)
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::27bfdf21f2d729136679b456a3e0363e
https://pubmed.ncbi.nlm.nih.gov/10678658
https://pubmed.ncbi.nlm.nih.gov/10678658
Publikováno v:
The Journal of urology. 148(5 Pt 2)
A total of 401 children with severe vesicoureteral reflux (97 with grade III and 304 with grade IV) was entered into the European branch of the International Reflux Study in Children. Of these patients 37 with grade III and 43 with grade IV reflux we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f3656267d9c6884547ba3b6260397e51
https://pubmed.ncbi.nlm.nih.gov/1433584
https://pubmed.ncbi.nlm.nih.gov/1433584
Autor:
U. Seppänen
Publikováno v:
Acta Radiologica. Diagnosis. 27:481-494
Despite the heterogeneous nature of congenital defects, an increasing number of aetiologically specific entities are being delineated, which is partly due to the increasing use of radiology. Data concerning the aetiology are especially important to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b1992d1925f99d8a475db743168cac9
https://doi.org/10.1177/028418518602700501
https://doi.org/10.1177/028418518602700501
Autor:
R. Herva, U. Seppänen
Publikováno v:
Pediatric Radiology. 13:329-331
The Meckel syndrome is an autosomal recessive lethal malformation syndrome. The main features are multicystic dysplastic kidneys, microcephaly with occipital encephalocele and polydactyly. This paper describes 6 new cases, with special reference to s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43a50371246c557f467be8a0f372330c
https://doi.org/10.1007/bf01625959
https://doi.org/10.1007/bf01625959
Publikováno v:
Rontgen-Blatter; Zeitschrift fur Rontgen-Technik und medizinisch-wissenschaftliche Photographie. 40(2)
Bronchial foreign bodies by children are dangerous and require immediate therapeutic measures. Findings and significance of chest film in the diagnosis of bronchial foreign bodies in 24 children were analysed. All patients were symptomatic. 18 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::27a5e2ff306e2b42e25b40aecfb31574
https://pubmed.ncbi.nlm.nih.gov/3563335
https://pubmed.ncbi.nlm.nih.gov/3563335
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 99(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f7101fa75453874be1ea5ac14a716ba
https://pubmed.ncbi.nlm.nih.gov/6884244
https://pubmed.ncbi.nlm.nih.gov/6884244
Autor:
U. Seppänen, R. Herva
Publikováno v:
Pediatric radiology. 14(1)
The hydrolethalus syndrome is an autosomal recessive malformation syndrome which has been recently described in Finland. The name hydrolethalus refers to the main findings, namely polyhydramnios, hydrocephalus and lethality. The patients are either s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ddfcde6973c1c8f937566a32e0255ab
https://pubmed.ncbi.nlm.nih.gov/6364021
https://pubmed.ncbi.nlm.nih.gov/6364021
Publikováno v:
European journal of pediatrics. 140(1)
A male infant with full 21-monosomy was identified by chromosome investigation. Clinical resemblance to the three former cases was obvious. Radiologic investigation showed unusual skeletal findings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b39e03e63a6b7a5418f3ce37cc564c7
https://pubmed.ncbi.nlm.nih.gov/6873114
https://pubmed.ncbi.nlm.nih.gov/6873114