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D Wittebol-Post

Showing results (31-40 of 39) with videos related to

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Ophthalmic Paediatrics and Genetics|March 1, 1992
Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch familyJ C Oosterwijk, M Nelen, P M Van Zandvoort, et al.
The British Journal of Ophthalmology|April 1, 1997
Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiencyI Schrijver-Wieling, G H van Rens, D Wittebol-Post, et al.
European Journal of Neurology|February 2, 2010
The clinical utility of MRI in patients with neurodevelopmental disorders of unknown originH M Engbers, R A J Nievelstein, R H J M Gooskens, et al.
Clinical Dysmorphology|October 1, 1993
The Peters'-Plus syndrome: description of 16 patients and review of the literatureR C Hennekam, M J Van Schooneveld, H H Ardinger, et al.
Developmental Medicine and Child Neurology|January 9, 1999
Visual, cognitive, and neurodevelopmental outcome at 51/2 years in children with perinatal haemorrhagic-ischaemic brain lesionsB M Van den Hout, P Eken, D Van der Linden, et al.
The American Journal of Medicine|August 1, 1994
Von Hippel-Lindau disease: new strategies in early detection and treatmentN Karsdorp, A Elderson, D Wittebol-Post, et al.
Brain Pathology (Zurich, Switzerland)|January 5, 2006
Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeatU Rüb, E R Brunt, K Gierga, et al.
The British Journal of Ophthalmology|April 2, 2009
A randomised comparison of bilateral recession versus unilateral recession-resection as surgery for infantile esotropiaJ-R Polling, M J C Eijkemans, J Esser, et al.
Stroke|June 1, 1996
Evaluation of the presence of premature atherosclerosis in adults with heterozygosity for cystathionine-beta-synthase deficiencyH W de Valk, M K van Eeden, J D Banga, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Ophthalmic Paediatrics and Genetics|March 1, 1992
Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch familyJ C Oosterwijk, M Nelen, P M Van Zandvoort, et al.
The British Journal of Ophthalmology|April 1, 1997
Retinal dystrophy in long chain 3-hydroxy-acyl-coA dehydrogenase deficiencyI Schrijver-Wieling, G H van Rens, D Wittebol-Post, et al.
European Journal of Neurology|February 2, 2010
The clinical utility of MRI in patients with neurodevelopmental disorders of unknown originH M Engbers, R A J Nievelstein, R H J M Gooskens, et al.
Clinical Dysmorphology|October 1, 1993
The Peters'-Plus syndrome: description of 16 patients and review of the literatureR C Hennekam, M J Van Schooneveld, H H Ardinger, et al.
Developmental Medicine and Child Neurology|January 9, 1999
Visual, cognitive, and neurodevelopmental outcome at 51/2 years in children with perinatal haemorrhagic-ischaemic brain lesionsB M Van den Hout, P Eken, D Van der Linden, et al.
The American Journal of Medicine|August 1, 1994
Von Hippel-Lindau disease: new strategies in early detection and treatmentN Karsdorp, A Elderson, D Wittebol-Post, et al.
Brain Pathology (Zurich, Switzerland)|January 5, 2006
Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeatU Rüb, E R Brunt, K Gierga, et al.
The British Journal of Ophthalmology|April 2, 2009
A randomised comparison of bilateral recession versus unilateral recession-resection as surgery for infantile esotropiaJ-R Polling, M J C Eijkemans, J Esser, et al.
Stroke|June 1, 1996
Evaluation of the presence of premature atherosclerosis in adults with heterozygosity for cystathionine-beta-synthase deficiencyH W de Valk, M K van Eeden, J D Banga, et al.
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