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H Puy

Showing results (41-50 of 68) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|April 19, 2006
[Type B natriuretic peptide (BNP) versus n-terminal type B natriuretic propeptide in the diagnosis of cardiac failure in the elderly over 75 population]R El Mahmoud, Y Alibay, D Brun-Ney, et al.
The Journal of Clinical Investigation|January 1, 1996
Increased delta aminolevulinic acid and decreased pineal melatonin production. A common event in acute porphyria studies in the ratH Puy, J C Deybach, A Bogdan, et al.
Human Molecular Genetics|March 1, 1996
Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyriaJ C Deybach, H Puy, A M Robréau, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|March 10, 2009
Excessive erythrocyte PPIX influences the hematologic status and iron metabolism in patients with dominant erythropoietic protoporphyriaC Delaby, S Lyoumi, S Ducamp, et al.
Critical Care Medicine|October 22, 1998
Nitric oxide synthase inhibition and the induction of cytochrome P-450 affect heme oxygenase-1 messenger RNA expression after partial hepatectomy and acute inflammation in ratsS Lyoumi, H Puy, F Tamion, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
American Journal of Human Genetics|June 1, 1997
Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.
Human Genetics|October 13, 2000
Porphobilinogen deaminase gene in African and Afro-Caribbean ethnic groups: mutations causing acute intermittent porphyria and specific intragenic polymorphismsA M Robreau-Fraolini, H Puy, C Aquaron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresisD Tchernitchko, J Lamoril, H Puy, et al.
Journal of Internal Medicine|November 14, 1997
Acute intermittent porphyria: prevalence of mutations in the porphobilinogen deaminase gene in blood donors in FranceY Nordmann, H Puy, V Da Silva, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Archives Des Maladies Du Coeur Et Des Vaisseaux|April 19, 2006
[Type B natriuretic peptide (BNP) versus n-terminal type B natriuretic propeptide in the diagnosis of cardiac failure in the elderly over 75 population]R El Mahmoud, Y Alibay, D Brun-Ney, et al.
The Journal of Clinical Investigation|January 1, 1996
Increased delta aminolevulinic acid and decreased pineal melatonin production. A common event in acute porphyria studies in the ratH Puy, J C Deybach, A Bogdan, et al.
Human Molecular Genetics|March 1, 1996
Mutations in the protoporphyrinogen oxidase gene in patients with variegate porphyriaJ C Deybach, H Puy, A M Robréau, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|March 10, 2009
Excessive erythrocyte PPIX influences the hematologic status and iron metabolism in patients with dominant erythropoietic protoporphyriaC Delaby, S Lyoumi, S Ducamp, et al.
Critical Care Medicine|October 22, 1998
Nitric oxide synthase inhibition and the induction of cytochrome P-450 affect heme oxygenase-1 messenger RNA expression after partial hepatectomy and acute inflammation in ratsS Lyoumi, H Puy, F Tamion, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
American Journal of Human Genetics|June 1, 1997
Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.
Human Genetics|October 13, 2000
Porphobilinogen deaminase gene in African and Afro-Caribbean ethnic groups: mutations causing acute intermittent porphyria and specific intragenic polymorphismsA M Robreau-Fraolini, H Puy, C Aquaron, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresisD Tchernitchko, J Lamoril, H Puy, et al.
Journal of Internal Medicine|November 14, 1997
Acute intermittent porphyria: prevalence of mutations in the porphobilinogen deaminase gene in blood donors in FranceY Nordmann, H Puy, V Da Silva, et al.
Pageof 7