Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon
- Author
- TERWINDT, G. M1 ; HAAN, J1 2 ; OPHOFF, R. A1 3 ; GROENEN, S. M. A1 ; STORIMANS, C. W. J. M4 ; LANSER, J. B. K5 ; ROOS, R. A. C1 ; BLEEKER-WAGEMAKERS, E. M6 ; FRANTS, R. R2 ; FERRARI, M. D1
[1] Department of Neurology, Leiden University Medical Centre, Leiden, Netherlands
[2] Department of Neurology, Rijnland Hospital, Leiderdorp, Netherlands
[3] Department of Anthropogenetics, Leiden University Medical Centre, Leiden, Netherlands
[4] Department of Ophthalmology, University Hospital Utrecht, Utrecht, Netherlands
[5] Department of Neuropsychology, Leiden University Medical Centre, Leiden, Netherlands
[6] Netherlands Ophthalmic Research Institute, Amsterdam, Netherlands - Source
Brain. 1998, Vol 121, pp 303-316 ; 2 ; ref : 3 p.1/4
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Association morbide Caractère autosomique Douleur Etude familiale Exploration Homme Liaison génétique Maladie héréditaire Migraine Raynaud syndrome Rétinopathie vasculaire Symptomatologie Acrosyndrome Appareil circulatoire pathologie Capillaire sanguin pathologie Cérébrovasculaire pathologie Encéphale pathologie Oeil pathologie Peau pathologie Système nerveux autonome pathologie Système nerveux central pathologie Système nerveux pathologie Vaisseau sanguin pathologie
- Keyword (en)
- Concomitant disease Autosomal character Pain Family study Exploration Human Linkage Genetic disease Migraine Raynaud phenomenon Vascular retinopathy Symptomatology Acrosyndrome Cardiovascular disease Capillary vessel disease Cerebrovascular disease Cerebral disorder Eye disease Skin disease Diseases of the autonomic nervous system Central nervous system disease Nervous system diseases Vascular disease
- Keyword (es)
- Asociación morbosa Carácter autosómico Dolor Estudio familiar Exploración Hombre Ligamiento genético Enfermedad hereditaria Jaqueca Raynaud síndrome Retinopatía vascular Sintomatología Acrosíndrome Aparato circulatorio patología Capilar sanguíneo patología Vaso sanguíneo encéfalo patología Encéfalo patología Ojo patología Piel patología Sistema nervioso autónomo patología Sistema nervosio central patología Sistema nervioso patología Vaso sanguíneo patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17C Vascular diseases and vascular malformations of the nervous system
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2149634
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1093/brain/121.2.303 
https://dx.doi.org/10.1093/brain/121.2.303
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