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Cephalalgia : an International Journal of Headache
|
January 30, 2009
Quality of life in children with primary headache in a general hospital
J Bruijn, W-F Arts, H Duivenvoorden, et al.
Neuropediatrics
|
February 1, 1995
Cerebellar and brainstem hypoplasia in a child with a partial monosomy for the short arm of chromosome 5 and partial trisomy for the short arm of chromosome 10
W F Arts, Y Hofstee, G F Drejer, et al.
Developmental Medicine and Child Neurology
|
August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1
J F de Rijk-van Andel, W F Arts, P G Barth, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 17, 2004
Hereditary porencephaly: clinical and MRI findings in two Dutch families
G M S Mancini, I F M de Coo, M H Lequin, et al.
Neuroradiology
|
January 1, 1991
Neuroimaging in lissencephaly type I
J F de Rijk-van Andel, M S van der Knaap, J Valk, et al.
Neuroepidemiology
|
January 1, 1991
Epidemiology of lissencephaly type I
J F de Rijk-van Andel, W F Arts, A Hofman, et al.
Neuropediatrics
|
August 1, 1985
Late-onset globoid cell leucodystrophy (Krabbe's disease). Clinical and genetic delineation of two forms and their relation to the early-infantile form
M C Loonen, O P Van Diggelen, H C Janse, et al.
The British Journal of Dermatology
|
January 1, 1985
Segmental neurofibromatosis
A P Oranje, V D Vuzevski, T J Kalis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 23, 1998
The first unprovoked, untreated seizure in childhood: a hospital based study of the accuracy of the diagnosis, rate of recurrence, and long term outcome after recurrence. Dutch study of epilepsy in childhood
H Stroink, O F Brouwer, W F Arts, et al.
American Journal of Human Genetics
|
January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14q
B B de Vries, W F Arts, G J Breedveld, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 50) with videos related to
Sort By:
Page
of 5
Cephalalgia : an International Journal of Headache
|
January 30, 2009
Quality of life in children with primary headache in a general hospital
J Bruijn, W-F Arts, H Duivenvoorden, et al.
Neuropediatrics
|
February 1, 1995
Cerebellar and brainstem hypoplasia in a child with a partial monosomy for the short arm of chromosome 5 and partial trisomy for the short arm of chromosome 10
W F Arts, Y Hofstee, G F Drejer, et al.
Developmental Medicine and Child Neurology
|
August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1
J F de Rijk-van Andel, W F Arts, P G Barth, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 17, 2004
Hereditary porencephaly: clinical and MRI findings in two Dutch families
G M S Mancini, I F M de Coo, M H Lequin, et al.
Neuroradiology
|
January 1, 1991
Neuroimaging in lissencephaly type I
J F de Rijk-van Andel, M S van der Knaap, J Valk, et al.
Neuroepidemiology
|
January 1, 1991
Epidemiology of lissencephaly type I
J F de Rijk-van Andel, W F Arts, A Hofman, et al.
Neuropediatrics
|
August 1, 1985
Late-onset globoid cell leucodystrophy (Krabbe's disease). Clinical and genetic delineation of two forms and their relation to the early-infantile form
M C Loonen, O P Van Diggelen, H C Janse, et al.
The British Journal of Dermatology
|
January 1, 1985
Segmental neurofibromatosis
A P Oranje, V D Vuzevski, T J Kalis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 23, 1998
The first unprovoked, untreated seizure in childhood: a hospital based study of the accuracy of the diagnosis, rate of recurrence, and long term outcome after recurrence. Dutch study of epilepsy in childhood
H Stroink, O F Brouwer, W F Arts, et al.
American Journal of Human Genetics
|
January 13, 2000
Benign hereditary chorea of early onset maps to chromosome 14q
B B de Vries, W F Arts, G J Breedveld, et al.
Page
of 5