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P Sarda

Showing results (71-80 of 150) with videos related to

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Journal of Medical Genetics|May 19, 2001
Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformationG Lefort, P Blanchet, A M Chaze, et al.
Annales De Genetique|January 1, 1993
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French familyG Lefort, J Taib, A Toutain, et al.
Annals of Hematology|November 28, 2002
Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemiaA F Remacha, J C Souto, E Rámila, et al.
Presse Medicale (Paris, France : 1983)|March 31, 1990
[Limitations of prenatal treatment of congenital toxoplasmosis with a sulfadiazine-pyrimethamine combination]P Boulot, F Pratlong, P Sarda, et al.
Human Genetics|April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation testS Tuffery, S Chambert, C Bareil, et al.
Lipids|July 1, 1993
Nervonic acid in red blood cell sphingomyelin in premature infants: an index of myelin maturation?F Babin, P Sarda, B Limasset, et al.
Molecular Human Reproduction|February 6, 2003
First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markersA Girardet, S Hamamah, T Anahory, et al.
Journal of Medical Genetics|December 1, 1998
Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random associationA Verloes, C Curry, M Jamar, et al.
American Journal of Obstetrics and Gynecology|October 28, 1998
Fatty acid desaturase activities and polyunsaturated fatty acid composition in human liver between the seventeenth and thirty-sixth gestational weeksA Rodriguez, P Sarda, C Nessmann, et al.
Journal of Health Economics and Outcomes Research|January 9, 2023
Burden of Comorbidities and Healthcare Resource Utilization Among Medicaid-Enrolled Extremely Premature InfantsMeredith E Mowitz, Wei Gao, Heather Sipsma, et al.
Pageof 15

Showing results (71-80 of 150) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|May 19, 2001
Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformationG Lefort, P Blanchet, A M Chaze, et al.
Annales De Genetique|January 1, 1993
X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome. Report of three male patients in a large French familyG Lefort, J Taib, A Toutain, et al.
Annals of Hematology|November 28, 2002
Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemiaA F Remacha, J C Souto, E Rámila, et al.
Presse Medicale (Paris, France : 1983)|March 31, 1990
[Limitations of prenatal treatment of congenital toxoplasmosis with a sulfadiazine-pyrimethamine combination]P Boulot, F Pratlong, P Sarda, et al.
Human Genetics|April 17, 1998
Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation testS Tuffery, S Chambert, C Bareil, et al.
Lipids|July 1, 1993
Nervonic acid in red blood cell sphingomyelin in premature infants: an index of myelin maturation?F Babin, P Sarda, B Limasset, et al.
Molecular Human Reproduction|February 6, 2003
First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markersA Girardet, S Hamamah, T Anahory, et al.
Journal of Medical Genetics|December 1, 1998
Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random associationA Verloes, C Curry, M Jamar, et al.
American Journal of Obstetrics and Gynecology|October 28, 1998
Fatty acid desaturase activities and polyunsaturated fatty acid composition in human liver between the seventeenth and thirty-sixth gestational weeksA Rodriguez, P Sarda, C Nessmann, et al.
Journal of Health Economics and Outcomes Research|January 9, 2023
Burden of Comorbidities and Healthcare Resource Utilization Among Medicaid-Enrolled Extremely Premature InfantsMeredith E Mowitz, Wei Gao, Heather Sipsma, et al.
Pageof 15