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J P Ardissone

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Acta Virologica|August 1, 1987
Enzyme secretion by human endothelial cells infected with Rickettsia conoriiD Raoult, A M Drancourt, J P Ardissone
La Nouvelle Presse Medicale|January 28, 1978
[When to assay creatine kinase isoenzyme MB?]G Lévy, J Romette, J P Ardissone, et al.
Human Heredity|January 1, 1980
Is the HpO phenomenon in tropical populations really genetic?A Rougemont, M Quilici, J Delmont, et al.
Pediatrie|July 1, 1973
[Results of simultaneous detection of hyperphenylalaninemia and congenital toxoplasmosis in the newborn (39,000 cases)]R Bernard, E Louchet, R Mariani, et al.
Clinical Genetics|February 1, 1980
Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1J F Mattei, M G Mattei, J P Ardissone, et al.
Human Genetics|January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8pJ F Mattei, M G Mattei, J P Ardissone, et al.
Journal of Endocrinological Investigation|January 1, 1993
Endemic goiter in Morocco (Skoura-Toundoute areas in the high atlas)R Aquaron, K Zarrouck, M el Jarari, et al.
Acta Paediatrica Scandinavica|July 1, 1982
Erythrocyte superoxide dismutase and redox enzymes in trisomy 21J F Mattei, M A Baeteman, A Baret, et al.
Thrombosis and Haemostasis|June 30, 1989
Increased plasminogen activator inhibitor activity in non insulin dependent diabetic patients--relationship with plasma insulinI Juhan-Vague, C Roul, M C Alessi, et al.
Life Sciences|December 3, 1979
Peripheral and central 5-hydroxytryptamine in trisomy 21J P Ternaux, J F Mattei, M Faudon, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Acta Virologica|August 1, 1987
Enzyme secretion by human endothelial cells infected with Rickettsia conoriiD Raoult, A M Drancourt, J P Ardissone
La Nouvelle Presse Medicale|January 28, 1978
[When to assay creatine kinase isoenzyme MB?]G Lévy, J Romette, J P Ardissone, et al.
Human Heredity|January 1, 1980
Is the HpO phenomenon in tropical populations really genetic?A Rougemont, M Quilici, J Delmont, et al.
Pediatrie|July 1, 1973
[Results of simultaneous detection of hyperphenylalaninemia and congenital toxoplasmosis in the newborn (39,000 cases)]R Bernard, E Louchet, R Mariani, et al.
Clinical Genetics|February 1, 1980
Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication-deletion of chromosome 9 and gene dosage effect for adenylate kinase-1J F Mattei, M G Mattei, J P Ardissone, et al.
Human Genetics|January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8pJ F Mattei, M G Mattei, J P Ardissone, et al.
Journal of Endocrinological Investigation|January 1, 1993
Endemic goiter in Morocco (Skoura-Toundoute areas in the high atlas)R Aquaron, K Zarrouck, M el Jarari, et al.
Acta Paediatrica Scandinavica|July 1, 1982
Erythrocyte superoxide dismutase and redox enzymes in trisomy 21J F Mattei, M A Baeteman, A Baret, et al.
Thrombosis and Haemostasis|June 30, 1989
Increased plasminogen activator inhibitor activity in non insulin dependent diabetic patients--relationship with plasma insulinI Juhan-Vague, C Roul, M C Alessi, et al.
Life Sciences|December 3, 1979
Peripheral and central 5-hydroxytryptamine in trisomy 21J P Ternaux, J F Mattei, M Faudon, et al.
Pageof 2