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R Stanescu

Showing results (61-70 of 72) with videos related to

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Archives Francaises De Pediatrie|December 1, 1982
[Heterogeneity of formes frustes of Morquio's disease]P Maroteaux, V Stanescu, R Stanescu, et al.
Arthritis and Rheumatism|July 1, 1987
Histopathology of arthritis induced in rats by active immunization to mycobacterial antigens or by systemic transfer of T lymphocyte lines. A light and electron microscopic study of the articular surface using cationized ferritinR Stanescu, O Lider, W van Eden, et al.
Annales De Genetique|January 1, 1992
Lethal short limb dwarfism with dysmorphic face, omphalocele and severe ossification defect: Piepkorn syndrome or severe "boomerang dysplasia"?N Canki-Klain, V Stanescu, R Stanescu, et al.
Archives Francaises De Pediatrie|December 1, 1978
[Fibrochondrogenesis]F Lazzaroni-Fossati, V Stanescu, R Stanescu, et al.
American Journal of Medical Genetics|September 1, 1984
Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebraeP Maroteaux, V Stanescu, R Stanescu, et al.
Bone|January 1, 1991
Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragilityM P Muriel, J Bonaventure, R Stanescu, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|April 28, 2000
[Diffusion MRI and cerebral ischemia. When to calculate the coefficient of diffusion?]C Oppenheim, R Stanescu, D Dormont, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 8, 1998
A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) regionC Poirier, S Blot, M Fernandes, et al.
AJNR. American Journal of Neuroradiology|September 26, 2000
False-negative diffusion-weighted MR findings in acute ischemic strokeC Oppenheim, R Stanescu, D Dormont, et al.
American Journal of Medical Genetics|December 1, 1992
Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxityJ Bonaventure, R Stanescu, V Stanescu, et al.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Archives Francaises De Pediatrie|December 1, 1982
[Heterogeneity of formes frustes of Morquio's disease]P Maroteaux, V Stanescu, R Stanescu, et al.
Arthritis and Rheumatism|July 1, 1987
Histopathology of arthritis induced in rats by active immunization to mycobacterial antigens or by systemic transfer of T lymphocyte lines. A light and electron microscopic study of the articular surface using cationized ferritinR Stanescu, O Lider, W van Eden, et al.
Annales De Genetique|January 1, 1992
Lethal short limb dwarfism with dysmorphic face, omphalocele and severe ossification defect: Piepkorn syndrome or severe "boomerang dysplasia"?N Canki-Klain, V Stanescu, R Stanescu, et al.
Archives Francaises De Pediatrie|December 1, 1978
[Fibrochondrogenesis]F Lazzaroni-Fossati, V Stanescu, R Stanescu, et al.
American Journal of Medical Genetics|September 1, 1984
Opsismodysplasia: a new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebraeP Maroteaux, V Stanescu, R Stanescu, et al.
Bone|January 1, 1991
Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragilityM P Muriel, J Bonaventure, R Stanescu, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|April 28, 2000
[Diffusion MRI and cerebral ischemia. When to calculate the coefficient of diffusion?]C Oppenheim, R Stanescu, D Dormont, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 8, 1998
A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) regionC Poirier, S Blot, M Fernandes, et al.
AJNR. American Journal of Neuroradiology|September 26, 2000
False-negative diffusion-weighted MR findings in acute ischemic strokeC Oppenheim, R Stanescu, D Dormont, et al.
American Journal of Medical Genetics|December 1, 1992
Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxityJ Bonaventure, R Stanescu, V Stanescu, et al.
Pageof 8