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P Maury

Showing results (121-130 of 178) with videos related to

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Scandinavian Journal of Rheumatology|January 1, 1985
Human high-density lipoprotein associated amyloid A protein. Structural characteristics, relation to apo A-I and A-II concentrations, and plasma clearance kinetics in the ratC Ehnholm, A M Teppo, J J Ohisalo, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|November 14, 1997
Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implicationsC P Maury, K Sletten, N Totty, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1991
[The gene defect for Finnish hereditary amyloidosis has been found]C P Maury, J Kere, M Baumann, et al.
Pacing and Clinical Electrophysiology : PACE|October 20, 1999
Association between nonreentrant supraventricular tachycardia and atrioventricular node reentrant tachycardia: a presentation of dual AV node physiologyP Maury, M Zimmermann, J Metzger, et al.
Panminerva Medica|May 1, 1975
Effect of intranodular B.C.G. in 22 melanoma patientsL Israël, A Depierre, R Edelstein, et al.
Journal of Clinical Pathology|December 1, 1988
Serum amyloid A protein, apolipoprotein A-I, and apolipoprotein B during the course of acute myocardial infarctionC P Maury, K J Tötterman, C G Gref, et al.
British Medical Journal (Clinical Research Ed.)|April 30, 1983
Correlation of persistently high serum amyloid A protein and C-reactive protein concentrations with rapid progression of secondary amyloidosisH M Falck, C P Maury, A M Teppo, et al.
Genomics|July 1, 1992
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal diseaseC P Maury, J Kere, R Tolvanen, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Fibrillogenesis in gelsolin-related familial amyloidosisC P Maury, E L Nurmiaho-Lassila, G Boysen, et al.
Minerva Cardioangiologica|October 13, 2010
Primary electrical diseases diagnosis, genetic and managementP Maury, A Duparc, P Mondoly, et al.
Pageof 18

Showing results (121-130 of 178) with videos related to

Sort By:
Pageof 18
Scandinavian Journal of Rheumatology|January 1, 1985
Human high-density lipoprotein associated amyloid A protein. Structural characteristics, relation to apo A-I and A-II concentrations, and plasma clearance kinetics in the ratC Ehnholm, A M Teppo, J J Ohisalo, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|November 14, 1997
Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implicationsC P Maury, K Sletten, N Totty, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1991
[The gene defect for Finnish hereditary amyloidosis has been found]C P Maury, J Kere, M Baumann, et al.
Pacing and Clinical Electrophysiology : PACE|October 20, 1999
Association between nonreentrant supraventricular tachycardia and atrioventricular node reentrant tachycardia: a presentation of dual AV node physiologyP Maury, M Zimmermann, J Metzger, et al.
Panminerva Medica|May 1, 1975
Effect of intranodular B.C.G. in 22 melanoma patientsL Israël, A Depierre, R Edelstein, et al.
Journal of Clinical Pathology|December 1, 1988
Serum amyloid A protein, apolipoprotein A-I, and apolipoprotein B during the course of acute myocardial infarctionC P Maury, K J Tötterman, C G Gref, et al.
British Medical Journal (Clinical Research Ed.)|April 30, 1983
Correlation of persistently high serum amyloid A protein and C-reactive protein concentrations with rapid progression of secondary amyloidosisH M Falck, C P Maury, A M Teppo, et al.
Genomics|July 1, 1992
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal diseaseC P Maury, J Kere, R Tolvanen, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|December 3, 2003
Fibrillogenesis in gelsolin-related familial amyloidosisC P Maury, E L Nurmiaho-Lassila, G Boysen, et al.
Minerva Cardioangiologica|October 13, 2010
Primary electrical diseases diagnosis, genetic and managementP Maury, A Duparc, P Mondoly, et al.
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