Zobrazeno 1 - 10
of 362
pro vyhledávání: '"H, Forsius"'
Publikováno v:
Hereditas. 57:373-381
Autor:
H. Forsius
Publikováno v:
Acta Ophthalmologica. 66:71-85
This introductory lecture to the epidemiological session in the Workshop on the Exfoliation Syndrome (ES) gathers together figures for the prevalence of ES around the world. Prevalence figures from published reports are shown in the text separately f
Publikováno v:
Acta Ophthalmologica. 47:1135-1148
Publikováno v:
Acta Ophthalmologica. 46:542-552
Autor:
H, FORSIUS, P, METSAELAE
Publikováno v:
Acta Ophthalmologica. 41:768-776
Autor:
U. Krause, H. Forsius
Publikováno v:
Acta Ophthalmologica. 46:1251-1255
Autor:
Aldur W. Eriksson, D. B. van Dorp, A.Th.M. van Balen, H. Collewijn, A. G. M. van Vliet, J.W. Delleman, H. Forsius
Publikováno v:
Clinical Genetics. 28:526-531
Electrophysiological studies showed that a patient with Aland eye disease had no misrouting of the optic pathways which is always found in all forms of albinism as a consequence of the retino-geniculate anomaly. Also the spontaneous and optokinetic n
An extensive electronystagmographical examination was made of 25 members of a family with Aland eye disease (Forsius-Eriksson syndrome). It appears that the nystagmus belongs to the syndrome of latent nystagmus. Out of seven investigated male subject
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7226d15bfc00791901de5f96884768e6
https://doi.org/10.1159/000392708
https://doi.org/10.1159/000392708
Autor:
Anne Rantala, A. W. Eriksson, A de la Chapelle, Johan Fellman, Laura Huopaniemi, H. Forsius, Tiina Alitalo
Publikováno v:
Annals of Human Genetics. 63:521-533
Carriers of X-linked juvenile retinoschisis (RS) were previously suggested to give birth to an excess of boys. We determined the carrier status for the 214G > A mutation of the RS1 gene in 202 females belonging to a large RS founder pedigree. The sec