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Vallat

Showing results (661-670 of 909) with videos related to

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Plos One|May 1, 2020
Epithelial changes of congenital intestinal obstruction in a rat modelQuentin Ballouhey, Laurent Fourcade, Laurence Richard, et al.
Pediatric Neurosurgery|September 10, 1998
Focal cortical dysplasia with glioproliferative changes causing seizures: report of 3 casesJ R Madsen, A V Vallat, T Y Poussaint, et al.
Neurology|June 1, 1997
Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous systemL Magy, N Birouk, J M Vallat, et al.
Annals of the New York Academy of Sciences|December 10, 1999
The absence of myelin P0 protein produces a novel molecular phenotype in Schwann cellsD M Menichella, W Xu, H Jiang, et al.
The British Journal of Dermatology|March 22, 2001
HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern FranceO Dereure, P Aguilar-Martinez, D Bessis, et al.
The Journal of Clinical Investigation|March 15, 2019
Anti-Neurofascin-155 IgG4 antibodies prevent paranodal complex formation in vivoConstance Manso, Luis Querol, Cinta Lleixà, et al.
Revue Neurologique|May 1, 1974
[Peripheral neuropathies in Waldenström's disease. 5 cases with ultrastructural study of the peripheral nerve]C Vital, P Henry, P Loiseau, et al.
Current Protocols|July 18, 2024
Describing and Sharing Molecular Visualizations Using the MolViewSpec ToolkitSebastian Bittrich, Adam Midlik, Mihaly Varadi, et al.
Revue Neurologique|August 31, 2010
[Management of stroke in sub-Saharan Africa: current issues]T A Adoukonou, J-M Vallat, J Joubert, et al.
Annales D'Anatomie Pathologique|March 1, 1975
[Peripheral neuropathies i- Waldenstrom's disease. Histological and ultrastructural studies of 5 cases]C Vital, P Henry, P Loiseau, et al.
Pageof 91

Showing results (661-670 of 909) with videos related to

Sort By:
Pageof 91
Plos One|May 1, 2020
Epithelial changes of congenital intestinal obstruction in a rat modelQuentin Ballouhey, Laurent Fourcade, Laurence Richard, et al.
Pediatric Neurosurgery|September 10, 1998
Focal cortical dysplasia with glioproliferative changes causing seizures: report of 3 casesJ R Madsen, A V Vallat, T Y Poussaint, et al.
Neurology|June 1, 1997
Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous systemL Magy, N Birouk, J M Vallat, et al.
Annals of the New York Academy of Sciences|December 10, 1999
The absence of myelin P0 protein produces a novel molecular phenotype in Schwann cellsD M Menichella, W Xu, H Jiang, et al.
The British Journal of Dermatology|March 22, 2001
HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern FranceO Dereure, P Aguilar-Martinez, D Bessis, et al.
The Journal of Clinical Investigation|March 15, 2019
Anti-Neurofascin-155 IgG4 antibodies prevent paranodal complex formation in vivoConstance Manso, Luis Querol, Cinta Lleixà, et al.
Revue Neurologique|May 1, 1974
[Peripheral neuropathies in Waldenström's disease. 5 cases with ultrastructural study of the peripheral nerve]C Vital, P Henry, P Loiseau, et al.
Current Protocols|July 18, 2024
Describing and Sharing Molecular Visualizations Using the MolViewSpec ToolkitSebastian Bittrich, Adam Midlik, Mihaly Varadi, et al.
Revue Neurologique|August 31, 2010
[Management of stroke in sub-Saharan Africa: current issues]T A Adoukonou, J-M Vallat, J Joubert, et al.
Annales D'Anatomie Pathologique|March 1, 1975
[Peripheral neuropathies i- Waldenstrom's disease. Histological and ultrastructural studies of 5 cases]C Vital, P Henry, P Loiseau, et al.
Pageof 91