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R Aquaron

Showing results (51-60 of 66) with videos related to

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Journal of Endocrinological Investigation|January 1, 1993
Endemic goiter in Morocco (Skoura-Toundoute areas in the high atlas)R Aquaron, K Zarrouck, M el Jarari, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|February 1, 1997
Acute intermittent porphyria: rapid molecular diagnosisH Puy, R Aquaron, J Lamoril, et al.
Revue Neurologique|September 24, 2008
[McArdle disease (gycogenosis type V): analysis of clinical, biological and genetic features of five French patients]E Delmont, S Sacconi, J-L Berge-Lefranc, et al.
Human Genetics|October 28, 1997
Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P geneN Puri, D Durbam-Pierre, R Aquaron, et al.
Annales D'Endocrinologie|July 1, 1972
[Effects of synthetic TRH in normal subjects]P Jaquet, J L Codaccioni, P Bordarier, et al.
Collegium Antropologicum|March 31, 1999
Epidemiology and prophylaxis of endemic goitre in the Bwa village of Sirao (Mali)F Roux, G Bellis, A A Rhaly, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1990
[Metabolic risks in surgical hysteroscopy]L Boubli, B Blanc, E Bautrand, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|March 25, 2006
[Oculocutaneous albinism in French overseas territories (Reunion, French Guyana, Martinique) and Mayotte. Study of 21 cases in 16 families]R Aquaron, J L Berge-Lefranc, C Badens, 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.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|May 1, 1972
[Muscular involvement in rheumatoid polyarthritis. Clinical, electromyographic, anatomopathological and biochemical study]H Roux, A M Recordier, G Serratrice, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
Journal of Endocrinological Investigation|January 1, 1993
Endemic goiter in Morocco (Skoura-Toundoute areas in the high atlas)R Aquaron, K Zarrouck, M el Jarari, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|February 1, 1997
Acute intermittent porphyria: rapid molecular diagnosisH Puy, R Aquaron, J Lamoril, et al.
Revue Neurologique|September 24, 2008
[McArdle disease (gycogenosis type V): analysis of clinical, biological and genetic features of five French patients]E Delmont, S Sacconi, J-L Berge-Lefranc, et al.
Human Genetics|October 28, 1997
Type 2 oculocutaneous albinism (OCA2) in Zimbabwe and Cameroon: distribution of the 2.7-kb deletion allele of the P geneN Puri, D Durbam-Pierre, R Aquaron, et al.
Annales D'Endocrinologie|July 1, 1972
[Effects of synthetic TRH in normal subjects]P Jaquet, J L Codaccioni, P Bordarier, et al.
Collegium Antropologicum|March 31, 1999
Epidemiology and prophylaxis of endemic goitre in the Bwa village of Sirao (Mali)F Roux, G Bellis, A A Rhaly, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1990
[Metabolic risks in surgical hysteroscopy]L Boubli, B Blanc, E Bautrand, et al.
Medecine Tropicale : Revue Du Corps De Sante Colonial|March 25, 2006
[Oculocutaneous albinism in French overseas territories (Reunion, French Guyana, Martinique) and Mayotte. Study of 21 cases in 16 families]R Aquaron, J L Berge-Lefranc, C Badens, 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.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|May 1, 1972
[Muscular involvement in rheumatoid polyarthritis. Clinical, electromyographic, anatomopathological and biochemical study]H Roux, A M Recordier, G Serratrice, et al.
Pageof 7