Zobrazeno 1 - 10
of 47
pro vyhledávání: '"R. ten Houten"'
Publikováno v:
Tijdschrift voor kindergeneeskunde. 73:80-85
Wij beschrijven een jongen van 15 maanden met een herseninfarct, bij wie er een relatie wordt vermoed met een doorgemaakte waterpokkeninfectie. De etiologie, kenmerken en behandeling worden besproken.
Autor:
Rune R. Frants, R ten Houten, Gerard Hageman, Rfm de Coo, Oebele F. Brouwer, E. H. van den Boogerd, P. M. Callenbach, Jan C. Oosterwijk, Amjm van den Maagdenberg
Publikováno v:
Clinical Genetics. 67:517-525
Benign familial infantile convulsions (BFIC) is an autosomal dominantly inherited partial epilepsy syndrome of early childhood with remission before the age of 3 years. The syndrome has been linked to loci on chromosomes 1q23, 2q24, 16p12-q12, and 19
Autor:
P M C, Callenbach, E H, van den Boogerd, R F M, de Coo, R, ten Houten, J C, Oosterwijk, G, Hageman, R R, Frants, O F, Brouwer, A M J M, van den Maagdenberg
Publikováno v:
Clinical genetics. 67(6)
Benign familial infantile convulsions (BFIC) is an autosomal dominantly inherited partial epilepsy syndrome of early childhood with remission before the age of 3 years. The syndrome has been linked to loci on chromosomes 1q23, 2q24, 16p12-q12, and 19
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(23)
Three patients, men aged 62, 57 and 44 years, had suffered for 6-24 months from low back pain, which after an acute moment had worsened with pain radiating to one leg. In all 3 patients, a neurological cause was considered first, but investigations r
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(14)
Two boys, aged 2 and 11 years, presented with fever and muscle weakness that resulted in respiratory insufficiency. A physical examination and additional tests confirmed the diagnosis 'myasthenia'. Acetyl cholinesterase-inhibitor therapy had a favour
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 141(42)
Four children aged 2.5 years, 15.7 and 7 months, including a pair of twins, after birth displayed hypotonia which necessitated tube feeding. Other features were a narrow forehead and a thin triangular upper lip, but these abnormalities were not consp
Autor:
R. ten Houten, R. J. A. Wanders, W. C. G. Overweg-Plandsoen, N. G. G. M. Abeling, A. H. van Gennip, J. F. van den Blij, Henk D. Bakker
Publikováno v:
Journal of inherited metabolic disease, 16(5), 900-901. Springer Netherlands
Publikováno v:
Tijdschrift voor kindergeneeskunde. 59(3)
Infants and children with achondroplasia are at increased risk of sudden death because of apneic attacks caused by compression of the medulla oblongata or spinal cord by a constricted foramen magnum or narrow upper cervical spinal canal. This history
Autor:
E. M. van Lie Peters, H. G. Loggers, R. ten Houten, Rja Wanders, F. A. Wijburg, Pieter A. Bolhuis, Peter G. Barth, A. van Wilsem, Nicole H. Herzberg, Wim Ruitenbeek, G. D. Vos
Publikováno v:
Journal of inherited metabolic disease, 14(3), 297-300. Springer Netherlands
Autor:
P. M. Callenbach, Paul B. Augustijn, O.F. Brouwer, W.B. Gunning, Hans Stroink, A.M. Weber, Willem F. M. Arts, Els A. J. Peeters, Y. Geerts, R. ten Houten
Publikováno v:
European Journal of Paediatric Neurology. 11:85