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L VAN BOGAERT

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Bulletin De L'Academie Royale De Medecine De Belgique|January 1, 1971
[Life and work of Prof. R. Garcin, foreign correspondent]L Van Bogaert
Monatsschrift Fur Psychiatrie Und Neurologie|March 19, 2010
On a hereditary-familial affection akin to Hallervorden-Spatz disease and cerebellar atrophies, characterized by a cerebellar-monoclonal syndrome progressing slowly and late a rigid state during neurofibromatosisL VAN BOGAERT
Journal Belge De Neurologie Et De Psychiatrie|March 19, 2010
The histopathological method and the problems of white matter diseasesL VAN BOGAERT
Annales Medico-Psychologiques|October 29, 2010
Association of a familial cerebral atrophy and a pallido-crosslinked pigmentary state (Hallervorden-Spatz) during neurofibromatosisL VAN BOGAERT
Annales Paediatrici. International Review of Pediatrics|March 19, 2010
Histological aspect of a late sequence of nuclear icterusL VAN BOGAERT
Acta Neurologica Belgica|January 1, 1974
[Farewell, Mr. Ley]L Van Bogaert
Journal of the Neurological Sciences|April 1, 1972
[J. Euziere (1882-1971)]L van Bogaert
Journal Belge De Neurologie Et De Psychiatrie|March 19, 2010
On a cortical cortical atrophy with the onset of axial sclerosis and involvement of the central gray nuclei: mental disorders: symmetrical lipomatosisL VAN BOGAERT, P BORREMANS
Journal of Neurology, Neurosurgery, and Psychiatry|March 19, 2010
A familial disease characterized by diffuse cortico-meningeal non-calcifying angiomatosis and progressive demyelination of the white substanceP DIVRY, L VAN BOGAERT
Bulletin De L'Academie Royale De Medecine De Belgique|January 1, 1970
[On the value of topography and structuring of nervous lesions in comparative anatomy. II. Apropos of lesions of the pregeniculate optic system, of spinal ganglions, roots and nerves in human and animal viroses]L Van Bogaert, A Taraszewska
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Bulletin De L'Academie Royale De Medecine De Belgique|January 1, 1971
[Life and work of Prof. R. Garcin, foreign correspondent]L Van Bogaert
Monatsschrift Fur Psychiatrie Und Neurologie|March 19, 2010
On a hereditary-familial affection akin to Hallervorden-Spatz disease and cerebellar atrophies, characterized by a cerebellar-monoclonal syndrome progressing slowly and late a rigid state during neurofibromatosisL VAN BOGAERT
Journal Belge De Neurologie Et De Psychiatrie|March 19, 2010
The histopathological method and the problems of white matter diseasesL VAN BOGAERT
Annales Medico-Psychologiques|October 29, 2010
Association of a familial cerebral atrophy and a pallido-crosslinked pigmentary state (Hallervorden-Spatz) during neurofibromatosisL VAN BOGAERT
Annales Paediatrici. International Review of Pediatrics|March 19, 2010
Histological aspect of a late sequence of nuclear icterusL VAN BOGAERT
Acta Neurologica Belgica|January 1, 1974
[Farewell, Mr. Ley]L Van Bogaert
Journal of the Neurological Sciences|April 1, 1972
[J. Euziere (1882-1971)]L van Bogaert
Journal Belge De Neurologie Et De Psychiatrie|March 19, 2010
On a cortical cortical atrophy with the onset of axial sclerosis and involvement of the central gray nuclei: mental disorders: symmetrical lipomatosisL VAN BOGAERT, P BORREMANS
Journal of Neurology, Neurosurgery, and Psychiatry|March 19, 2010
A familial disease characterized by diffuse cortico-meningeal non-calcifying angiomatosis and progressive demyelination of the white substanceP DIVRY, L VAN BOGAERT
Bulletin De L'Academie Royale De Medecine De Belgique|January 1, 1970
[On the value of topography and structuring of nervous lesions in comparative anatomy. II. Apropos of lesions of the pregeniculate optic system, of spinal ganglions, roots and nerves in human and animal viroses]L Van Bogaert, A Taraszewska
Pageof 3