Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Susann Andersson"'
Publikováno v:
Acta Ophthalmologica. 100:673-681
To map the morphology of the retina and optic disc in adolescents with surgically treated hydrocephalus (HC) in infancy and to compare the results with healthy controls.The study comprised 26 adolescents (16 male, mean age 15 years) with HC and 31 se
Publikováno v:
Acta Ophthalmologica. 92:682-688
Purpose The purpose was to characterize normal growth patterns of ocular and optical components and to relate them to auxological data in a sample of Swedish children aged 4–15 years. Methods A prospective cross-sectional study was carried out in 1
Autor:
Rebecka Åkebrand, Antovan K. Seyedi Honarvar, Marita Andersson Grönlund, Kalliopi Sofou, Niklas Darin, Susann Andersson, M. Tulinius
Publikováno v:
Acta ophthalmologica. 95(1)
Autor:
Ann Hellström, Susann Andersson
Publikováno v:
British Journal of Ophthalmology. 93:526-530
Aims: To investigate the morphology of the optic disc and retinal vessels in children with surgically treated hydrocephalus. Methods: A prospective, population-based study was performed in 69 children (median age 9.6 years) with early surgically trea
Autor:
Niklas Darin, Kalliopi Sofou, Antovan K. Seyedi Honarvar, Susann Andersson, Marita Andersson Grönlund, Rebecka Åkebrand, Mar Tulinius
Publikováno v:
Acta ophthalmologica. 94(6)
Purpose To describe ophthalmological characteristics in children with Leigh syndrome (LS), an inherited, progressive, mitochondrial encephalomyopathy, at diagnosis and over time, and relate the results to causative genetic mutations. Methods Forty-fo
Publikováno v:
Acta Ophthalmologica Scandinavica. 84:169-176
Aims: To characterize ophthalmological findings in a sample of Swedish children aged 4–15 years. Methods: A prospective cross-sectional comprehensive ophthalmological investigation was performed on a sample of 143 children (67 girls, 76 boys) aged
Autor:
Elisabeth Holme, Anders Oldfors, M. Andersson Grönlund, M. Tulinius, A-R. Moslemi, Gittan Kollberg, Niklas Darin, Susann Andersson
Publikováno v:
Neuromuscular Disorders. 16:504-506
We describe a second patient with the 583G>A mutation in the tRNA(phe) gene of mitochondrial DNA (mtDNA). This 17-year-old girl had a mitochondrial myopathy with exercise intolerance and an asymptomatic retinopathy. Muscle investigations showed occas
Autor:
E Holme, Susann Andersson, A K Seyedi Honarvar, Niklas Darin, A R Moslemi, M. Tulinius, A Oldfors, Marita Andersson Grönlund
Publikováno v:
The British journal of ophthalmology. 94(1)
Aim: To describe ophthalmological phenotypes in patients with mitochondrial disease and known genotypes. Methods: A retrospective study was performed on 59 patients (29 male, 30 female) with a mean age of 11.8 years who had mitochondrial disease with
Autor:
Eva Aring, Susann Andersson, Anna-Lena Hård, Ann Hellström, Eva-Karin Persson, Paul Uvebrant, Jan Ygge
Publikováno v:
Strabismus. 15(2)
To investigate heterotropia, heterophoria, head posture, nystagmus, stereo acuity, ocular motility and near point of convergence (NPC) in children with hydrocephalus treated surgically before 1 year of age. In addition, the effects of being born with
Autor:
Marita Andersson Grönlund, Jan Ygge, Anna-Lena Hård, Ann Hellström, Susann Andersson, Eva Aring
Publikováno v:
Strabismus. 13(2)
To investigate strabismus, head posture, nystagmus, stereoacuity, ocular motility, near point of convergence (NPC) and accommodative convergence to accommodation ratio (AC/A) in a sample of Swedish children.A prospective cross-sectional study was car