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J Y Peltier

Showing results (11-20 of 17) with videos related to

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La Revue De Medecine Interne|October 20, 2000
[Activated C protein resistance manifested by cutaneous necrosis after interferon alpha injection: case report]F Plurien, Z Le Lostec, C Pauwels, et al.
Thrombosis Research|October 24, 2001
Three new cases of dysfibrinogenemia: Poissy III, Saint-Germain I and TahitiF Mathonnet, J Y Peltier, L Roda, et al.
Clinical Chemistry|May 20, 1998
An improved method for the detection of the thermolabile variant of methylenetetrahydrofolate reductaseG Van Amerongen, F Mathonnet, C Boucly, et al.
Thrombosis Research|April 29, 1998
An improved method for the detection of the G20210A transition in the prothrombin geneM Raoul, F Mathonnet, J Y Peltier, et al.
Blood|November 1, 1994
Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell DiseaseM Maier-Redelsperger, C T Noguchi, M de Montalembert, et al.
International Journal of Laboratory Hematology|July 31, 2010
Routine diagnostic procedures of myelodysplastic syndromes: value of a structural blood cell parameter (NEUT-X) determined by the Sysmex XE-2100™G Le Roux, A Vlad, V Eclache, et al.
European Journal of Haematology|April 25, 2000
Iron overload in thalassaemias and genetic haemochromatosisP Aguilar-Martinez, J F Schved, C Badens, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
La Revue De Medecine Interne|October 20, 2000
[Activated C protein resistance manifested by cutaneous necrosis after interferon alpha injection: case report]F Plurien, Z Le Lostec, C Pauwels, et al.
Thrombosis Research|October 24, 2001
Three new cases of dysfibrinogenemia: Poissy III, Saint-Germain I and TahitiF Mathonnet, J Y Peltier, L Roda, et al.
Clinical Chemistry|May 20, 1998
An improved method for the detection of the thermolabile variant of methylenetetrahydrofolate reductaseG Van Amerongen, F Mathonnet, C Boucly, et al.
Thrombosis Research|April 29, 1998
An improved method for the detection of the G20210A transition in the prothrombin geneM Raoul, F Mathonnet, J Y Peltier, et al.
Blood|November 1, 1994
Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell DiseaseM Maier-Redelsperger, C T Noguchi, M de Montalembert, et al.
International Journal of Laboratory Hematology|July 31, 2010
Routine diagnostic procedures of myelodysplastic syndromes: value of a structural blood cell parameter (NEUT-X) determined by the Sysmex XE-2100™G Le Roux, A Vlad, V Eclache, et al.
European Journal of Haematology|April 25, 2000
Iron overload in thalassaemias and genetic haemochromatosisP Aguilar-Martinez, J F Schved, C Badens, et al.
Pageof 2