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P G Barth

Showing results (41-50 of 177) with videos related to

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Clinical Genetics|August 1, 1984
Mosaic tetrasomy 21 in a male childM L Kwee, P G Barth, F Arwert, et al.
Brain & Development|January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasiaP 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 encephaloceleF 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 phenotypeE 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 newbornP G Barth, F C Stam, J J von der Harten
Child'S Brain|January 1, 1981
Congenital multiple angiomatosis with brain involvementL 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 entityA 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 disorderL 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 studyJ Assies, L J Gooren, B Van Geel, et al.
European Journal of Pediatrics|August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal colobomaD Lindhout, P G Barth, J Valk, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
Clinical Genetics|August 1, 1984
Mosaic tetrasomy 21 in a male childM L Kwee, P G Barth, F Arwert, et al.
Brain & Development|January 1, 1982
Familial lissencephaly with extreme neopallial hypoplasiaP 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 encephaloceleF 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 phenotypeE 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 newbornP G Barth, F C Stam, J J von der Harten
Child'S Brain|January 1, 1981
Congenital multiple angiomatosis with brain involvementL 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 entityA 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 disorderL 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 studyJ Assies, L J Gooren, B Van Geel, et al.
European Journal of Pediatrics|August 1, 1980
The Joubert syndrome associated with bilateral chorioretinal colobomaD Lindhout, P G Barth, J Valk, et al.
Pageof 18