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Waasdorp, C.M.
( C.M. Waasdorp)
complication children nf 1 patients study group prevalence neurofibromatosi patient symptom neurofibroma glioma disorder incidence pathway pathway glioma plexiform behavioural problems problem presentation incidence rates criteria abnormality examination date plexiform neurofibromas person-year neurofibromatosis type 1 cafu lait spots group b 18 years child examination endocrinological disease table article cnossen 11 december 2006 speech van den ouweland nf 1 diagnosis behavioural diagnosis motor disorders pathway gliomas lisch nodules university risk factors huson goede-bolder disease features development 0.3 december sophia nf 1. hospital thorax abnormalities motor number van den broek h j simonsz downloaded paediatric 1 january 1996 von recklinghausen neurofibromatosis children 6 years 100 person-years adc.bmj.com malignancy j j halley factor group c paediatric neurologist brain retardation analysis broek department 2.0 oranje
1 Most Recent Publications
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A prospective 10 year follow up study of patients with neurofibromatosis type 1
(Article)
Cnossen, M.H. Goede-Bolder, A. de Broek, K.M. van den Waasdorp, C.M. Oranje, A.P. Stroink, H. Simonsz, H.J. Ouweland, A.M.W. van den Halley, D.J.J. Niermeijer, M.F. |
1998-01-01
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