Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mieke M. C. Bijveld"'
Autor:
Mieke M C Bijveld, Maria M van Genderen, Frank P Hoeben, Amir A Katzin, Ruth M A van Nispen, Frans C C Riemslag, Astrid M L Kappers
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e62927 (2013)
Congenital Stationary Night Blindness (CSNB) is a retinal disorder caused by a signal transmission defect between photoreceptors and bipolar cells. CSNB can be subdivided in CSNB2 (rod signal transmission reduced) and CSNB1 (rod signal transmission a
Externí odkaz:
https://doaj.org/article/2fbacc0c497a4118bdcbb3bb5e6b7c8a
Autor:
Gerard C. de Wit, Florine Pilon, Maria M. van Genderen, Marjoke J. Dekker, Mieke M. C. Bijveld
Publikováno v:
Strabismus. 20:49-54
To determine normal values of the crowding ratio (CR) in children.Of 62 normally sighted primary school children aged 4-12 years old the CR was determined both for distance and near vision. The examinations were performed using commonly available tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08924928aa81c0fd3f991bf6db746e8
https://doi.org/10.3109/09273972.2012.680233
https://doi.org/10.3109/09273972.2012.680233
Autor:
Liesbeth Prick, Maria M. van Genderen, Maarten Kamermans, Ralph J. Florijn, Astrid M. L. Kappers, Arthur A.B. Bergen, Frans C. C. Riemslag, Mieke M. C. Bijveld, L. Ingeborgh van den Born, Mary J. van Schooneveld
Publikováno v:
Ophthalmology, 120, 2072-2081. Elsevier B.V.
Bijveld, M M C, Florijn, R J, Bergen, A A B, van den Born, L I, Kamermans, M, Prick, L, Riemslag, F C C, van Schooneveld, M J, Kappers, A M L & van Genderen, M M 2013, ' Genotype and Phenotype of 101 Dutch Patients with Congenital Stationary Night Blindness ', Ophthalmology, vol. 120, no. 10, pp. 2072-2081 . https://doi.org/10.1016/j.ophtha.2013.03.002
Ophthalmology, 120(10), 2072-2081. Elsevier Inc.
Bijveld, M M C, Florijn, R J, Bergen, A A B, van den Born, L I, Kamermans, M, Prick, L, Riemslag, F C C, van Schooneveld, M J, Kappers, A M L & van Genderen, M M 2013, ' Genotype and Phenotype of 101 Dutch Patients with Congenital Stationary Night Blindness ', Ophthalmology, vol. 120, no. 10, pp. 2072-2081 . https://doi.org/10.1016/j.ophtha.2013.03.002
Ophthalmology, 120(10), 2072-2081. Elsevier Inc.
Objective: To investigate the relative frequency of the genetic causes of the Schubert-Bornschein type of congenital stationary night blindness (CSNB) and to determine the genotype-phenotype correlations in CSNB1 and CSNB2. Design: Clinic-based, long
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d07eb224e736828b67241f70612f728
https://pure.knaw.nl/portal/en/publications/bf5d0039-9329-4cc6-b3e0-1d4e198a0adc
https://pure.knaw.nl/portal/en/publications/bf5d0039-9329-4cc6-b3e0-1d4e198a0adc
Autor:
Maria M. van Genderen, Frank P. Hoeben, Ruth M. A. van Nispen, Astrid M. L. Kappers, Mieke M. C. Bijveld, Frans C. C. Riemslag, Amir A. Katzin
Publikováno v:
Bijveld, M M C, van Genderen, M M, Hoeben, F P, Katzin, A A, van Nispen, R M A, Riemslag, F C C & Kappers, A M L 2013, ' Assessment of Night Vision Problems in Patients with Congenital Stationary Night Blindness ', PLoS ONE, vol. 8, no. 5, e62927 . https://doi.org/10.1371/journal.pone.0062927
PLoS ONE, 8(5):e62927. Public Library of Science
PLoS ONE, Vol 8, Iss 5, p e62927 (2013)
PLoS ONE
PLoS ONE, 8(5):e62927. Public Library of Science
PLoS ONE, Vol 8, Iss 5, p e62927 (2013)
PLoS ONE
Congenital Stationary Night Blindness (CSNB) is a retinal disorder caused by a signal transmission defect between photoreceptors and bipolar cells. CSNB can be subdivided in CSNB2 (rod signal transmission reduced) and CSNB1 (rod signal transmission a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::237147fbedc4326563f42301ccbc6eb2
https://research.vu.nl/en/publications/4ba98c28-9a38-43e5-b878-e696f68ab796
https://research.vu.nl/en/publications/4ba98c28-9a38-43e5-b878-e696f68ab796
Autor:
Frans C. C. Riemslag, Frank P. Hoeben, Mieke M. C. Bijveld, Astrid M. L. Kappers, Anne C. L. Vrijling, Maria M. van Genderen
Publikováno v:
Documenta ophthalmologica. Advances in ophthalmology. 123(3)
The minimum in the amplitude versus flash strength curve of dark-adapted 15 Hz electroretinograms (ERGs) has been attributed to interactions between the primary and secondary rod pathways. The 15 Hz ERGs can be used to examine the two rod pathways in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1198979bc4e8891fb6328bcaee506695
https://pubmed.ncbi.nlm.nih.gov/21947561
https://pubmed.ncbi.nlm.nih.gov/21947561
Autor:
Maarten Kamermans, Jillian N. Pearring, Maureen A. McCall, Arthur A.B. Bergen, Mieke M. C. Bijveld, Frans C. C. Riemslag, Maria M. van Genderen, Y. Claassen, Ralph J. Florijn, Ronald G. Gregg, Françoise Meire
Publikováno v:
American Journal of Human Genetics, 85, 730-736. Cell Press
American journal of human genetics, 85(5), 730-736. Cell Press
The American Journal of Human Genetics; Vol 85
American journal of human genetics, 85(5), 730-736. Cell Press
The American Journal of Human Genetics; Vol 85
Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive impaired night vision and variable decreased visual acuity. We report here that six out of eight fem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::557de094a207dd7523f85e10b2e303c6
https://pure.knaw.nl/portal/en/publications/b90e003e-d893-47dc-a204-7fd504a60cbc
https://pure.knaw.nl/portal/en/publications/b90e003e-d893-47dc-a204-7fd504a60cbc