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Neurology
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January 1, 1990
The juvenile and chronic forms of GM2 gangliosidosis: clinical and enzymatic heterogeneity
N Specola, M T Vanier, F Goutières, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates
J S Sequeira, A Vellodi, M T Vanier, et al.
Brain & Development
|
October 2, 2001
Sites and temporal changes of gangliosides GM1/GM2 storage in the Niemann-Pick disease type C mouse brain
M Taniguchi, Y Shinoda, H Ninomiya, et al.
Revue Neurologique
|
June 1, 1997
[Isolated spastic paraparesis disclosing Krabbe disease in adult age]
M Bataillard, P Richard, L Rumbach, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1993
Fetal Niemann-Pick disease type C: ultrastructural and lipid findings in liver and spleen
C Dumontel, C Girod, F Dijoud, et al.
Acta Paediatrica Scandinavica
|
May 1, 1975
Polyunsaturated fatty acid lipidosis. II. Lipid biochemical studies
L Svennerholm, B Hagberg, M Haltia, et al.
European Journal of Pediatrics
|
February 14, 1998
Early-lethal pulmonary form of Niemann-Pick type C disease belonging to a second, rare genetic complementation group
O Schofer, B Mischo, W Püschel, et al.
The Journal of Biological Chemistry
|
April 10, 1973
Structure of the major glucosamine-containing ganglioside of human tissues
Y T Li, J E Månsson, M T Vanier, et al.
Archives Francaises De Pediatrie
|
January 1, 1991
[Cataplexy revealing an atypical form of Niemann-Pick disease type C]
C Denoix, C Rodriguez-Lafrasse, M T Vanier, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
November 2, 1999
Talin concentrates to the midbody region during mammalian cell cytokinesis
A Bellissent-Waydelich, M T Vanier, C Albigès-Rizo, et al.
Page
of 16
Search research articles
Search
Showing results (51-60 of 156) with videos related to
Sort By:
Page
of 16
Neurology
|
January 1, 1990
The juvenile and chronic forms of GM2 gangliosidosis: clinical and enzymatic heterogeneity
N Specola, M T Vanier, F Goutières, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates
J S Sequeira, A Vellodi, M T Vanier, et al.
Brain & Development
|
October 2, 2001
Sites and temporal changes of gangliosides GM1/GM2 storage in the Niemann-Pick disease type C mouse brain
M Taniguchi, Y Shinoda, H Ninomiya, et al.
Revue Neurologique
|
June 1, 1997
[Isolated spastic paraparesis disclosing Krabbe disease in adult age]
M Bataillard, P Richard, L Rumbach, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1993
Fetal Niemann-Pick disease type C: ultrastructural and lipid findings in liver and spleen
C Dumontel, C Girod, F Dijoud, et al.
Acta Paediatrica Scandinavica
|
May 1, 1975
Polyunsaturated fatty acid lipidosis. II. Lipid biochemical studies
L Svennerholm, B Hagberg, M Haltia, et al.
European Journal of Pediatrics
|
February 14, 1998
Early-lethal pulmonary form of Niemann-Pick type C disease belonging to a second, rare genetic complementation group
O Schofer, B Mischo, W Püschel, et al.
The Journal of Biological Chemistry
|
April 10, 1973
Structure of the major glucosamine-containing ganglioside of human tissues
Y T Li, J E Månsson, M T Vanier, et al.
Archives Francaises De Pediatrie
|
January 1, 1991
[Cataplexy revealing an atypical form of Niemann-Pick disease type C]
C Denoix, C Rodriguez-Lafrasse, M T Vanier, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
November 2, 1999
Talin concentrates to the midbody region during mammalian cell cytokinesis
A Bellissent-Waydelich, M T Vanier, C Albigès-Rizo, et al.
Page
of 16