Zobrazeno 1 - 10
of 13
pro vyhledávání: '"S E Tangsrud"'
Publikováno v:
Respiratory Medicine. 95(11):898-903
Duchenne's muscular dystrophy (DMD), characterized by gradually developing muscular weakness, leads to respiratory symptoms and reduced lung function. We aimed to assess lung function in 25 patients with DMD in relationship to age and muscular functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b847000b8ac6cf225abe7b51fc86fd1
Autor:
I, Lund-Petersen, S E, Tangsrud
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 121(22)
Information from parents of children with neuromuscular diseases and from the children 16 years later is used to discuss specialist medical care towards this group in view of new treatment possibilities and the Norwegian health and social service ref
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c2f3780c997449b2a0ebe6588bcbfe1
https://pubmed.ncbi.nlm.nih.gov/11668756
https://pubmed.ncbi.nlm.nih.gov/11668756
BACKGROUNDSpinal muscular atrophy (SMA) affects respiratory muscles, which in addition to progressive scoliosis leads to respiratory impairment. Children with developing scoliosis are usually treated with spinal bracing to delay the progress.AIMSTo a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82c512d65ec7c44dbbd85c52b3ce3116
https://europepmc.org/articles/PMC1718814/
https://europepmc.org/articles/PMC1718814/
Severe craniofacial malformations and deglutition dysfunction in a brother and sister: new syndrome?
Publikováno v:
American journal of medical genetics. 78(3)
We report seemingly unique craniofacial malformations and deglutition dysfunction in a sib pair. The boy had right maxillomandibular alveolar synechae, ankylosis of right temporomandibular joint, hypoplasia of the zygomatico-maxillary region, nasal d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d56f1ea746a26a97c31138188cbd787
https://pubmed.ncbi.nlm.nih.gov/9677062
https://pubmed.ncbi.nlm.nih.gov/9677062
Publikováno v:
Journal of medical genetics. 29(11)
The orofaciodigital syndromes are a group of possibly seven different malformation syndromes including oral, facial, and digital malformations. Type I has X linked dominant inheritance whereas the other types show autosomal recessive inheritance. An
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0e327125a48d4949021bc0870d682d1
https://pubmed.ncbi.nlm.nih.gov/1453437
https://pubmed.ncbi.nlm.nih.gov/1453437
Publikováno v:
Acta Paediatrica. 71:711-715
In the present study, auditory brainstem responses (ABR) were recorded in 60 high-risk neonates in the intensive care unit selected by the following criteria: Birth-weight less than 2000 g, hyperbilirubinemia requiring phototherapy or exchange transf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98ade16bdc8c214157b83ac70a287f1c
https://doi.org/10.1111/j.1651-2227.1982.tb09508.x
https://doi.org/10.1111/j.1651-2227.1982.tb09508.x
Autor:
S E, Tangsrud
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 98(16)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::507ee2e33b9bd25c8785277d4c26d57b
https://pubmed.ncbi.nlm.nih.gov/675628
https://pubmed.ncbi.nlm.nih.gov/675628
Publikováno v:
Acta paediatrica Scandinavica. 68(4)
Scleroderma in a two-year-old boy with gross enlargement of the right inguinal lymph nodes, as an early sign, is reported. Repeated lymph node biopsies revealed non-characteristic reactive changes and hyperplasia, but eventually histological examinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e57c9a6a8523073087a24e172aea69c4
https://pubmed.ncbi.nlm.nih.gov/463550
https://pubmed.ncbi.nlm.nih.gov/463550
Autor:
S. Halvorsen, S. E. Tangsrud
Publikováno v:
Acta paediatrica Scandinavica. 78(1)
In a survey carried out to determine the incidence of Duchenne muscular dystrophy in South East Norway, 38 cases were ascertained among 149,975 live male births during the years 1968-1978. The overall incidence is 1:3,917 in live male births (25.33 x
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacfedeee7443a51bece3f50e2f8fe13
https://pubmed.ncbi.nlm.nih.gov/2784019
https://pubmed.ncbi.nlm.nih.gov/2784019
Autor:
E H, Strøm, S E, Tangsrud
Publikováno v:
Clinical neuropathology. 5(2)
This report describes a case of centronuclear myopathy which was considered to represent an example of severe x-linked myotubular myopathy [van Wijngaarden et al. 1969]. The neonatal period was dramatic with weak movements and respiratory problems. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7fdd071f9f1381d2fce38cfe12b2dfb
https://pubmed.ncbi.nlm.nih.gov/3708957
https://pubmed.ncbi.nlm.nih.gov/3708957