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Journal of Managed Care & Specialty Pharmacy|December 28, 2020
Paroxysmal nocturnal hemoglobinuria: current treatments and unmet needsMeryem Bektas, Catherine Copley-Merriman, Shahnaz Khan, et al.The Journal of Bone and Joint Surgery. British Volume|December 14, 2011
Tranexamic acid in total knee replacement: a systematic review and meta-analysisS Alshryda, P Sarda, M Sukeik, et al.Journal De Genetique Humaine|August 1, 1986
[Reinfection after rubella and congenital polymalformation syndrome]G Sibille, P Sarda, J Jalaguier, et al.Journal of Managed Care & Specialty Pharmacy|December 28, 2020
Paroxysmal nocturnal hemoglobinuria: patient journey and burden of diseaseMeryem Bektas, Catherine Copley-Merriman, Shahnaz Khan, et al.Annals of Nutrition & Metabolism|January 1, 1996
Relationships between red blood cell vitamin E and polyunsaturated fatty acid in the premature infantD Bouglé, A Nouvelot, C Billeaud, et al.Journal of Managed Care & Specialty Pharmacy|May 1, 2023
Geographic atrophy: Mechanism of disease, pathophysiology, and role of the complement systemSophie J Bakri, Meryem Bektas, Darcie Sharp, et al.Frontiers in Pediatrics|January 11, 2020
Health Care Burden of Bronchopulmonary Dysplasia Among Extremely Preterm InfantsMeredith E Mowitz, Rajeev Ayyagari, Wei Gao, et al.Human Reproduction (Oxford, England)|April 23, 2005
Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: a comparison of locus-specific probe and whole chromosome paintingT Anahory, S Hamamah, B Andréo, et al.Bulletin De L'Academie Nationale De Medecine|February 1, 1994
[Biological effects on premature neonates of a milk formula enriched with alpha-linolenic acid: a multicenter study]A Crastes de Paulet, F Babin, C Billeaud, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boyS Tuffery, P Moine, P Sarda, et al.Pageof 17