J-C Deybach - JoVE Visualize

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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 Clinical Pathology|January 1, 1996

Detection by PCR of Toxoplasma gondii in blood in the diagnosis of cerebral toxoplasmosis in patients with AIDSJ Lamoril, J M Molina, A de Gouvello, et al.

Human Genetics|March 1, 1993

High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, 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.

Antimicrobial Agents and Chemotherapy|April 1, 1985

Renal disposition of gentamicin, dibekacin, tobramycin, netilmicin, and amikacin in humansA Contrepois, N Brion, J J Garaud, 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.

Clinical Chemistry|January 1, 1992

Denaturing gradient gel electrophoresis for rapid detection of latent carriers of a subtype of acute intermittent porphyria with normal erythrocyte porphobilinogen deaminase activityF Bourgeois, X F Gu, J C Deybach, 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.

Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002

Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyriaU Gross, H Puy, A Kühnel, 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.

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Showing results (61-70 of 87) with videos related to

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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 Clinical Pathology|January 1, 1996

Detection by PCR of Toxoplasma gondii in blood in the diagnosis of cerebral toxoplasmosis in patients with AIDSJ Lamoril, J M Molina, A de Gouvello, et al.

Human Genetics|March 1, 1993

High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, 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.

Antimicrobial Agents and Chemotherapy|April 1, 1985

Renal disposition of gentamicin, dibekacin, tobramycin, netilmicin, and amikacin in humansA Contrepois, N Brion, J J Garaud, 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.

Clinical Chemistry|January 1, 1992

Denaturing gradient gel electrophoresis for rapid detection of latent carriers of a subtype of acute intermittent porphyria with normal erythrocyte porphobilinogen deaminase activityF Bourgeois, X F Gu, J C Deybach, 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.

Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002

Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyriaU Gross, H Puy, A Kühnel, 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.

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