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Journal of Inherited Metabolic Disease|January 1, 1994
Peroxisomal disorders: a reviewB Fournier, J A Smeitink, L Dorland, et al.
Presse Medicale (Paris, France : 1983)|November 26, 1994
[Reference values of lipoprotein(a) in a French population]J Steinmetz, P Tarallo, B Fournier, et al.
Blood|August 15, 1992
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin geneM Garbarz, L Boulanger, S Pedroni, et al.
Pharmacoepidemiology and Drug Safety|November 1, 2012
Identification of abuse and dependence cases through a hospital databaseA Daveluy, G Miremont-Salamé, A Kostrzewa, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1986
Hereditary elliptocytosis: clinical, morphological and biochemical studies of 38 casesD Dhermy, M Garbarz, M C Lecomte, et al.
Acta Crystallographica. Section D, Biological Crystallography|February 10, 2000
Towards the charge-density study of proteins: a room-temperature scorpion-toxin structure at 0.96 A resolution as a first test caseD Housset, F Benabicha, V Pichon-Pesme, et al.
Blood|November 1, 1984
A variant of erythrocyte membrane skeletal protein band 4.1 associated with hereditary elliptocytosisM Garbarz, D Dhermy, M C Lecomte, et al.
Medecine Et Maladies Infectieuses|August 29, 2012
[Ertapenem administered intravenously or subcutaneously for urinary tract infections caused by ESBL producing enterobacteriacea]E Forestier, S Gros, D Peynaud, et al.
The Journal of Clinical Investigation|August 1, 1994
Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophyB Fournier, J M Saudubray, B Benichou, et al.
The Review of Scientific Instruments|November 7, 2012
The x-ray source application test cassette for radiation exposures at the OMEGA laserK B Fournier, V Rekow, J Emig, et al.
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