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Decreased morbidity in homozygous sickle cell disease detected at birth.
Bardakdjian-Michau J, Guilloud-Batailie M, Maier-Redelsperger M, Elion J, Girot R, Feingold J, Galactéros F, de Montalembert M. Bardakdjian-Michau J, et al. Among authors: feingold j. Hemoglobin. 2002 Aug;26(3):211-7. doi: 10.1081/hem-120015024. Hemoglobin. 2002. PMID: 12403485
Implications of prenatal diagnosis of sickle cell disease.
de Montalembert M, Guilloud-Bataille M, Ducros A, Galacteros F, Girot R, Herve C, Maier-Redelsperger M, Feingold J. de Montalembert M, et al. Among authors: feingold j. Genet Couns. 1996;7(1):9-15. Genet Couns. 1996. PMID: 8652095
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections.
Neonato MG, Lu CY, Guilloud-Bataille M, Lapouméroulie C, Nabeel-Jassim H, Dabit D, Girot R, Krishnamoorthy R, Feingold J, Besmond C, Elion J. Neonato MG, et al. Among authors: feingold j. Eur J Hum Genet. 1999 Sep;7(6):679-86. doi: 10.1038/sj.ejhg.5200360. Eur J Hum Genet. 1999. PMID: 10482957
442 results