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P Rondot

Showing results (101-110 of 114) with videos related to

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Revue Neurologique|January 1, 1989
[X-ray computed tomography of lumbosacral roots and primary hypertrophic neuritis (Dejerine-Sottas disease)]J L Mas, D Buthiau, C Fallet-Bianco, et al.
Journal of Neuro-Oncology|October 1, 1991
Intravascular lymphomatosis (neoplastic angioendotheliosis) of the central nervous system: case report and literature reviewD Smadja, J L Mas, C Fallet-Bianco, et al.
Revue Neurologique|January 1, 1988
[Clinical, electrophysiologic and endocrine effects of the perfusion of high doses of TRH in amyotrophic lateral sclerosis]B Gueguen, J Puymirat, D Grouselle, et al.
Revue Neurologique|February 1, 1970
[Treatment of Parkinson's disease with L-dopa. 77 cases]G Boudin, P Castaigne, F Lhermitte, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Annales De Medecine Interne|August 1, 1973
[Recurrent familial hyperthyroidism with pseudomyopathic onset and central neurological involvment]P Doury, P L Chigot, J F Dulac, et al.
Annals of Human Genetics|March 14, 2001
Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonismR J Swaans, P Rondot, W O Renier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1991
(99mTc)-HM-PAO SPECT and cognitive impairment in Parkinson's disease: a comparison with dementia of the Alzheimer typeU Spampinato, M O Habert, J L Mas, et al.
Revue Neurologique|January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]B Eymard, E Morel, O Dulac, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Revue Neurologique|January 1, 1989
[X-ray computed tomography of lumbosacral roots and primary hypertrophic neuritis (Dejerine-Sottas disease)]J L Mas, D Buthiau, C Fallet-Bianco, et al.
Journal of Neuro-Oncology|October 1, 1991
Intravascular lymphomatosis (neoplastic angioendotheliosis) of the central nervous system: case report and literature reviewD Smadja, J L Mas, C Fallet-Bianco, et al.
Revue Neurologique|January 1, 1988
[Clinical, electrophysiologic and endocrine effects of the perfusion of high doses of TRH in amyotrophic lateral sclerosis]B Gueguen, J Puymirat, D Grouselle, et al.
Revue Neurologique|February 1, 1970
[Treatment of Parkinson's disease with L-dopa. 77 cases]G Boudin, P Castaigne, F Lhermitte, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Annales De Medecine Interne|August 1, 1973
[Recurrent familial hyperthyroidism with pseudomyopathic onset and central neurological involvment]P Doury, P L Chigot, J F Dulac, et al.
Annals of Human Genetics|March 14, 2001
Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonismR J Swaans, P Rondot, W O Renier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1991
(99mTc)-HM-PAO SPECT and cognitive impairment in Parkinson's disease: a comparison with dementia of the Alzheimer typeU Spampinato, M O Habert, J L Mas, et al.
Revue Neurologique|January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]B Eymard, E Morel, O Dulac, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Pageof 12