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M Cohen-Solal

Showing results (91-100 of 106) with videos related to

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Bone|January 1, 1994
Biologic, histologic and densitometric effects of oral risedronate on bone in patients with multiple myelomaC Roux, P Ravaud, M Cohen-Solal, et al.
Blood Cells, Molecules & Diseases|January 1, 1996
The 1591C mutation in triosephosphate isomerase (TPI) deficiency. Tightly linked polymorphisms and a common haplotype in all known familiesA Schneider, B Westwood, C Yim, et al.
Bone|September 20, 2005
LRP5 gene polymorphisms and idiopathic osteoporosis in menS L Ferrari, S Deutsch, C Baudoin, et al.
British Journal of Haematology|January 14, 1999
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry)M Cohen-Solal, C Préhu, H Wajcman, et al.
Annales De Medecine Interne|January 1, 1988
[Still's disease in adults: efficacy of corticosteroid pulses (a case)]M Cohen-Solal, P Fardellone, X Debussche, et al.
Nephron|January 1, 1989
Disappearance of aluminic bone disease in a long term asymptomatic dialysis population restricting A1(OH)3 intake: emergence of an idiopathic adynamic bone disease not related to aluminumP Morinière, M Cohen-Solal, S Belbrik, et al.
Gene|July 16, 1990
Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutaseJ Castella-Escola, D M Ojcius, P LeBoulch, et al.
The Journal of Biological Chemistry|November 15, 1989
Human bisphosphoglycerate mutase. Expression in Escherichia coli and use of site-directed mutagenesis in the evaluation of the role of the carboxyl-terminal region in the enzymatic mechanismM C Garel, V Joulin, P Le Boulch, et al.
Blood|July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)C Valentin, S Pissard, J Martin, et al.
Clinical Immunology and Immunopathology|July 1, 1995
Cytokine-mediated bone resorption in patients with the hyperimmunoglobulin E syndromeM Cohen-Solal, A M Prieur, L Prin, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Bone|January 1, 1994
Biologic, histologic and densitometric effects of oral risedronate on bone in patients with multiple myelomaC Roux, P Ravaud, M Cohen-Solal, et al.
Blood Cells, Molecules & Diseases|January 1, 1996
The 1591C mutation in triosephosphate isomerase (TPI) deficiency. Tightly linked polymorphisms and a common haplotype in all known familiesA Schneider, B Westwood, C Yim, et al.
Bone|September 20, 2005
LRP5 gene polymorphisms and idiopathic osteoporosis in menS L Ferrari, S Deutsch, C Baudoin, et al.
British Journal of Haematology|January 14, 1999
A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry)M Cohen-Solal, C Préhu, H Wajcman, et al.
Annales De Medecine Interne|January 1, 1988
[Still's disease in adults: efficacy of corticosteroid pulses (a case)]M Cohen-Solal, P Fardellone, X Debussche, et al.
Nephron|January 1, 1989
Disappearance of aluminic bone disease in a long term asymptomatic dialysis population restricting A1(OH)3 intake: emergence of an idiopathic adynamic bone disease not related to aluminumP Morinière, M Cohen-Solal, S Belbrik, et al.
Gene|July 16, 1990
Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutaseJ Castella-Escola, D M Ojcius, P LeBoulch, et al.
The Journal of Biological Chemistry|November 15, 1989
Human bisphosphoglycerate mutase. Expression in Escherichia coli and use of site-directed mutagenesis in the evaluation of the role of the carboxyl-terminal region in the enzymatic mechanismM C Garel, V Joulin, P Le Boulch, et al.
Blood|July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)C Valentin, S Pissard, J Martin, et al.
Clinical Immunology and Immunopathology|July 1, 1995
Cytokine-mediated bone resorption in patients with the hyperimmunoglobulin E syndromeM Cohen-Solal, A M Prieur, L Prin, et al.
Pageof 11