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Annals of the Rheumatic Diseases
|
November 1, 1970
Serum caeruloplasmin in rheumatology
H Roux, R Aquaron, R Grangier, et al.
Annales De Dermatologie Et De Venereologie
|
January 28, 2009
[New nonsense mutation (p.E250X) in the tyrosinase gene of a patient with oculocutaneous albinism type 1A]
R Aquaron, S Hesse, C Badens, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires
|
December 1, 1986
[AMP deaminase deficiency (myoadenylate deaminase). Disease or syndrome?]
G Serratrice, J F Pellissier, R Aquaron, et al.
La Revue De Medecine Interne
|
January 1, 1996
[Acute intermittent porphyria in 2 Moroccan families. Clinical and biological study]
R Aquaron, K Zarrouck, A el Boussaki, et al.
Revue Neurologique
|
January 1, 1995
[Parkinson disease and alkaptonuria: fortuitous association or striatonigral ochronosis?]
R Aquaron, G Fayet, C Barthet, et al.
Annales D'Endocrinologie
|
November 1, 1970
[Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. I. 4 new cases]
J L Codaccioni, H Pierron, R Rouault, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires
|
October 1, 1989
[Serum osteocalcin in rheumatologic practice]
O Costes, R Aquaron, J Courtois-Momburg, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires
|
February 1, 1971
[Determination of serum ceruloplasmin in rheumatology]
H Roux, R Aquaron, F Bergeaud, et al.
Annales D'Endocrinologie
|
July 1, 1972
[Study of hypophyso-thyroid function using synthetic TRH in thyroid pathology]
J L Codaccioni, R Aquaron, P Jaquet, et al.
Annales D'Endocrinologie
|
November 1, 1970
[Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. II. Results of iodine treatment in 5 cases (8 years of recession in 1 case]
J L Codaccioni, H Pierron, F Rouault, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 66) with videos related to
Sort By:
Page
of 7
Annals of the Rheumatic Diseases
|
November 1, 1970
Serum caeruloplasmin in rheumatology
H Roux, R Aquaron, R Grangier, et al.
Annales De Dermatologie Et De Venereologie
|
January 28, 2009
[New nonsense mutation (p.E250X) in the tyrosinase gene of a patient with oculocutaneous albinism type 1A]
R Aquaron, S Hesse, C Badens, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires
|
December 1, 1986
[AMP deaminase deficiency (myoadenylate deaminase). Disease or syndrome?]
G Serratrice, J F Pellissier, R Aquaron, et al.
La Revue De Medecine Interne
|
January 1, 1996
[Acute intermittent porphyria in 2 Moroccan families. Clinical and biological study]
R Aquaron, K Zarrouck, A el Boussaki, et al.
Revue Neurologique
|
January 1, 1995
[Parkinson disease and alkaptonuria: fortuitous association or striatonigral ochronosis?]
R Aquaron, G Fayet, C Barthet, et al.
Annales D'Endocrinologie
|
November 1, 1970
[Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. I. 4 new cases]
J L Codaccioni, H Pierron, R Rouault, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires
|
October 1, 1989
[Serum osteocalcin in rheumatologic practice]
O Costes, R Aquaron, J Courtois-Momburg, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires
|
February 1, 1971
[Determination of serum ceruloplasmin in rheumatology]
H Roux, R Aquaron, F Bergeaud, et al.
Annales D'Endocrinologie
|
July 1, 1972
[Study of hypophyso-thyroid function using synthetic TRH in thyroid pathology]
J L Codaccioni, R Aquaron, P Jaquet, et al.
Annales D'Endocrinologie
|
November 1, 1970
[Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. II. Results of iodine treatment in 5 cases (8 years of recession in 1 case]
J L Codaccioni, H Pierron, F Rouault, et al.
Page
of 7