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D Wittebol-Post

Showing results (21-30 of 39) with videos related to

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Developmental Medicine and Child Neurology|June 1, 1992
The prevalence of cerebral visual disturbance in children with cerebral palsyA J Schenk-Rootlieb, O van Nieuwenhuizen, Y van der Graaf, et al.
Journal of Pediatric Ophthalmology and Strabismus|January 1, 1996
Screening for retinopathy of prematurity: do former guidelines still apply?N E Schalij-Delfos, B L Zijlmans, D Wittebol-Post, et al.
Developmental Medicine and Child Neurology|September 24, 1998
Development of visual function in hemihydranencephalyG Porro, D Wittebol-Post, M de Graaf, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Less severe retinopathy of prematurity induced by surfactant replacement therapyJ Termote, N E Schalij-Delfos, B P Cats, et al.
Clinical Dysmorphology|October 29, 2002
Split hand/split foot, iris/choroid coloboma, hypospadias and subfertility: a new developmental malformation syndrome?J C Giltay, D Wittebol-Post, H van Bokhoven, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 24, 1997
Elevated ocular levels of vascular endothelial growth factor in patients with von Hippel-Lindau diseaseM Los, C J Aarsman, L Terpstra, et al.
European Journal of Pediatrics|February 1, 1994
Surfactant replacement therapy: a new risk factor in developing retinopathy of prematurity?J U Termote, N E Schalij-Delfos, D Wittebol-Post, et al.
The British Journal of Ophthalmology|January 30, 1999
Visual behaviours of neurologically impaired children with cerebral visual impairment: an ethological studyG Porro, E M Dekker, O Van Nieuwenhuizen, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 1, 1992
[Keratosis follicularis spinulosa decalvans (Siemens I syndrome), initial results of molecular genetic research]J C Oosterwijk, L D van Osch, D Wittebol-Post, et al.
American Journal of Human Genetics|April 1, 1992
Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2J C Oosterwijk, M Nelen, P M van Zandvoort, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Developmental Medicine and Child Neurology|June 1, 1992
The prevalence of cerebral visual disturbance in children with cerebral palsyA J Schenk-Rootlieb, O van Nieuwenhuizen, Y van der Graaf, et al.
Journal of Pediatric Ophthalmology and Strabismus|January 1, 1996
Screening for retinopathy of prematurity: do former guidelines still apply?N E Schalij-Delfos, B L Zijlmans, D Wittebol-Post, et al.
Developmental Medicine and Child Neurology|September 24, 1998
Development of visual function in hemihydranencephalyG Porro, D Wittebol-Post, M de Graaf, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Less severe retinopathy of prematurity induced by surfactant replacement therapyJ Termote, N E Schalij-Delfos, B P Cats, et al.
Clinical Dysmorphology|October 29, 2002
Split hand/split foot, iris/choroid coloboma, hypospadias and subfertility: a new developmental malformation syndrome?J C Giltay, D Wittebol-Post, H van Bokhoven, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 24, 1997
Elevated ocular levels of vascular endothelial growth factor in patients with von Hippel-Lindau diseaseM Los, C J Aarsman, L Terpstra, et al.
European Journal of Pediatrics|February 1, 1994
Surfactant replacement therapy: a new risk factor in developing retinopathy of prematurity?J U Termote, N E Schalij-Delfos, D Wittebol-Post, et al.
The British Journal of Ophthalmology|January 30, 1999
Visual behaviours of neurologically impaired children with cerebral visual impairment: an ethological studyG Porro, E M Dekker, O Van Nieuwenhuizen, et al.
Klinische Monatsblatter Fur Augenheilkunde|December 1, 1992
[Keratosis follicularis spinulosa decalvans (Siemens I syndrome), initial results of molecular genetic research]J C Oosterwijk, L D van Osch, D Wittebol-Post, et al.
American Journal of Human Genetics|April 1, 1992
Linkage analysis of keratosis follicularis spinulosa decalvans, and regional assignment to human chromosome Xp21.2-p22.2J C Oosterwijk, M Nelen, P M van Zandvoort, et al.
Pageof 4