Zobrazeno 1 - 10
of 150
pro vyhledávání: '"D. Wittebol-Post"'
Publikováno v:
Neural Plasticity, Vol 12, Iss 2-3, Pp 205-210 (2005)
Introduction: Deficient postural control is one of the key problems in cerebral palsy (CP). Little, however, is known about the specific nature of postural problems of children with CP, nor of the relation between abnormal posture and dysfunction of
Externí odkaz:
https://doaj.org/article/dd0dd1f6b2124bb6bd4500864973c78a
Autor:
V. Herzau, A. Zubcov, Joachim Esser, M. P. M. ten Tusscher, E. Schulz, P. Roggenkämper, G. H. Kolling, G. C. Gusek, Huib Simonsz, Marinus J.C. Eijkemans, D. Wittebol-Post, B. Lieb, Jan Roelof Polling, Birgit Lorenz
Publikováno v:
28th European Strabismological Association Meeting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4466d4a677ff04e200da72a20f5b5782
https://doi.org/10.1201/9781003077541-41
https://doi.org/10.1201/9781003077541-41
Autor:
H. Y. Kroes, Gepke Visser, D. Wittebol-Post, H. M. Engbers, R. Van Empelen, R. H. J. M. Gooskens, R. A. J. Nievelstein, O. Braams, M. M. W. B. Hendriks
Publikováno v:
European Journal of Neurology. 17:815-822
Introduction: Neuroimaging of the brain in the diagnostic work-up of patients with neurodevelopmental disorders is a matter of continuing debate. Recommendations range from performing brain imaging in all patients with neurodevelopmental disorders to
Autor:
Y T. Schouw, L S Vries, D. Linden, S. Aleman, A. Jennekens‐Schinkel, D. Wittebol‐Post, P. Eken, O Nienwenhuizen, B M. Hout
Publikováno v:
Developmental Medicine & Child Neurology. 40:820-828
To determine predictive values of early visual and neurocognitive assessment in children with perinatally acquired haemorrhagic or ischaemic brain lesions selected on the basis of ultrasound, 63 children (37 boys, 26 girls), who had been followed and
Autor:
Onno van Nieuwenhuizen, Giorgio L. Porro, D. Wittebol-Post, A. J. F. Schenk-Rootlieb, Miky Graaf, W F Treffers
Publikováno v:
Developmental Medicine & Child Neurology. 40:563-567
This study reports on the findings of longitudinal follow-up of visual function in a 12-year-old girl affected by congenital right hemihydranencephaly. This extremely rare unilateral brain malformation allowed the authors to gather new information on
Autor:
Helmut Heinsen, Thomas Deller, Kimihito Arai, Georg Auburger, Christian Schultz, Ewout R. Brunt, D. Wittebol-Post, Kay Seidel, W.F. Glimmerveen, D. Rai, Ludger Schöls, P. F. Ippel, K. Gierga, Udo Rüb
Publikováno v:
BRAIN PATHOLOGY, 15(4), 287-295. Wiley-Blackwell
Brain Pathol
Brain Pathol
Spinocerebellar ataxia type 7 (SCA7) represents a very rare and severe autosomal dominantly inherited cerebellar ataxia (ADCA). It belongs to the group of CAG-repeat or polyglutamine diseases with its underlying molecular genetical defect on chromoso
Publikováno v:
Clinical Dysmorphology, 11, 231-6
Clinical Dysmorphology, 11, 4, pp. 231-6
Clinical Dysmorphology, 11, 4, pp. 231-6
Item does not contain fulltext This paper presents a patient with the following malformations: split hand and split foot on the left side, a hypoplastic fifth ray of the right hand and a hypoplastic first ray of the right foot with a small cleft betw
Publikováno v:
International Journal of Oral and Maxillofacial Surgery. 36:858-860
Oculodentodigital dysplasia (ODDD) is a rare, autosomal dominant pleiotropic disorder, caused by mutations in the Connexin 43 (Cx43 or GJA1) gene. Described here is the case of a 10-year-old girl with enamel hypoplasia, typical facies and mental dela
Publikováno v:
Eye. 12:858-862
Purpose To analyse the natural course of visual acuity in subjects affected by cerebral palsy. Methods During the past 5 years, 16 children underwent repeated grating acuity measurements using the acuity card procedure. At the end of the follow-up fi
Publikováno v:
Journal of Child Neurology. 10:459-463
Charcot-Marie-Tooth disease comprises a heterogeneous group of neurologic disorders that share peripheral motor and sensory neuropathy. A classification of these disorders was proposed in 1975, defining seven types of hereditary motor and sensory neu