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Clinical Genetics
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August 1, 1984
Mosaic tetrasomy 21 in a male child
M L Kwee, P G Barth, F Arwert, et al.
Brain & Development
|
January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasia
P G Barth, R Mullaart, F C Stam, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 4, 2000
Subependymal nodular heterotopia in patients with encephalocele
F A Roelens, P G Barth, J J van der Harten
Neuropediatrics
|
June 21, 2002
"Vanishing white matter" and ovarian dysgenesis in an infant with cerebro-oculo-facio-skeletal phenotype
E Boltshauser, P G Barth, D Troost, et al.
Acta Neuropathologica
|
April 26, 1978
Tuberous sclerosis and dysplasia of the corpus callosum. Case report of their combined occurrence in a newborn
P G Barth, F C Stam, J J von der Harten
Child'S Brain
|
January 1, 1981
Congenital multiple angiomatosis with brain involvement
L M Smit, P G Barth, F C Stam, et al.
Clinical Neurology and Neurosurgery
|
August 1, 1994
Limb girdle muscular dystrophy: reappraisal of a rejected entity
A J van der Kooi, M de Visser, P G Barth
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1984
Paucity of secondary synaptic clefts in a case of congenital myasthenia with multiple contractures: ultrastructural morphology of a developmental disorder
L M Smit, F G Jennekens, H Veldman, et al.
International Journal of Andrology
|
September 1, 2005
Signs of testicular insufficiency in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy: a retrospective study
J Assies, L J Gooren, B Van Geel, et al.
European Journal of Pediatrics
|
August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal coloboma
D Lindhout, P G Barth, J Valk, et al.
Page
of 18
Search research articles
Search
Showing results (41-50 of 177) with videos related to
Sort By:
Page
of 18
Clinical Genetics
|
August 1, 1984
Mosaic tetrasomy 21 in a male child
M L Kwee, P G Barth, F Arwert, et al.
Brain & Development
|
January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasia
P G Barth, R Mullaart, F C Stam, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 4, 2000
Subependymal nodular heterotopia in patients with encephalocele
F A Roelens, P G Barth, J J van der Harten
Neuropediatrics
|
June 21, 2002
"Vanishing white matter" and ovarian dysgenesis in an infant with cerebro-oculo-facio-skeletal phenotype
E Boltshauser, P G Barth, D Troost, et al.
Acta Neuropathologica
|
April 26, 1978
Tuberous sclerosis and dysplasia of the corpus callosum. Case report of their combined occurrence in a newborn
P G Barth, F C Stam, J J von der Harten
Child'S Brain
|
January 1, 1981
Congenital multiple angiomatosis with brain involvement
L M Smit, P G Barth, F C Stam, et al.
Clinical Neurology and Neurosurgery
|
August 1, 1994
Limb girdle muscular dystrophy: reappraisal of a rejected entity
A J van der Kooi, M de Visser, P G Barth
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 1, 1984
Paucity of secondary synaptic clefts in a case of congenital myasthenia with multiple contractures: ultrastructural morphology of a developmental disorder
L M Smit, F G Jennekens, H Veldman, et al.
International Journal of Andrology
|
September 1, 2005
Signs of testicular insufficiency in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy: a retrospective study
J Assies, L J Gooren, B Van Geel, et al.
European Journal of Pediatrics
|
August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal coloboma
D Lindhout, P G Barth, J Valk, et al.
Page
of 18