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I Maire

Showing results (1-10 of 121) with videos related to

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Revue Francaise De Transfusion Et D'Hemobiologie : Bulletin De La Societe Nationale De Transfusion Sanguine|March 1, 1990
[Determination of the activity of alanine aminotransferase]I Maire
Journal of Inherited Metabolic Disease|January 5, 2002
Is genotype determination useful in predicting the clinical phenotype in lysosomal storage diseases?I Maire
Journal of Inherited Metabolic Disease|January 1, 1990
Possible diagnosis of type 1b glycogen storage disease using frozen liver biopsiesI Maire, M Mathieu
Clinical Chemistry|May 1, 1990
Interference of amikacin in thin-layer chromatographic screening of urine for oligosaccharidosisM Piraud, I Maire
Journal of Inherited Metabolic Disease|January 1, 1986
Possible prenatal diagnosis of type III glycogenosisI Maire, M Mathieu
Annales De Pathologie|December 31, 1997
[Diagnosis of lysosomal storage diseases with fetal presentation]R Bouvier, I Maire
Journal of Inherited Metabolic Disease|January 1, 1984
Human placenta: a convenient source of homologous material, for diagnosis and therapy of inborn errors of metabolismM Mathieu, I Maire
Annales De Biologie Clinique|January 1, 1980
Modification of a recommended method for the determination of catalytic concentration of creatine kinase in human serum at 30 degrees C (document C', stage 3)M Mathieu, I Maire
Journal of Inherited Metabolic Disease|January 1, 1989
First trimester prenatal diagnosis of glycogen storage disease type IIII Maire, G Mandon, M Mathieu
Clinical Chemistry|January 1, 1993
Pitfalls of screening for mucopolysaccharidoses by the dimethylmethylene blue testM Piraud, I Maire, M Mathieu
Pageof 13

Showing results (1-10 of 121) with videos related to

Sort By:
Pageof 13
Revue Francaise De Transfusion Et D'Hemobiologie : Bulletin De La Societe Nationale De Transfusion Sanguine|March 1, 1990
[Determination of the activity of alanine aminotransferase]I Maire
Journal of Inherited Metabolic Disease|January 5, 2002
Is genotype determination useful in predicting the clinical phenotype in lysosomal storage diseases?I Maire
Journal of Inherited Metabolic Disease|January 1, 1990
Possible diagnosis of type 1b glycogen storage disease using frozen liver biopsiesI Maire, M Mathieu
Clinical Chemistry|May 1, 1990
Interference of amikacin in thin-layer chromatographic screening of urine for oligosaccharidosisM Piraud, I Maire
Journal of Inherited Metabolic Disease|January 1, 1986
Possible prenatal diagnosis of type III glycogenosisI Maire, M Mathieu
Annales De Pathologie|December 31, 1997
[Diagnosis of lysosomal storage diseases with fetal presentation]R Bouvier, I Maire
Journal of Inherited Metabolic Disease|January 1, 1984
Human placenta: a convenient source of homologous material, for diagnosis and therapy of inborn errors of metabolismM Mathieu, I Maire
Annales De Biologie Clinique|January 1, 1980
Modification of a recommended method for the determination of catalytic concentration of creatine kinase in human serum at 30 degrees C (document C', stage 3)M Mathieu, I Maire
Journal of Inherited Metabolic Disease|January 1, 1989
First trimester prenatal diagnosis of glycogen storage disease type IIII Maire, G Mandon, M Mathieu
Clinical Chemistry|January 1, 1993
Pitfalls of screening for mucopolysaccharidoses by the dimethylmethylene blue testM Piraud, I Maire, M Mathieu
Pageof 13