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Human Genetics|December 1, 1987
Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expressionM C Lecomte, D Dhermy, M Garbarz, et al.
Blood|June 1, 1986
Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosisM Garbarz, M C Lecomte, D Dhermy, et al.
Prenatal Diagnosis|September 1, 1987
Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrinD Dhermy, C Feo, M Garbarz, et al.
Human Genetics|January 1, 1985
Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosisM C Lecomte, D Dhermy, M Garbarz, et al.
Pediatric Research|October 1, 1984
Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemiaD Dhermy, M C Lecomte, M Garbarz, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|February 1, 1997
Human coproporphyrinogen oxidase. Biochemical characterization of recombinant normal and R231W mutated enzymes expressed in E. coli as soluble, catalytically active homodimersP Martásek, J M Camadro, C S Raman, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1996
[Paraneoplastic pemphigus in chronic lymphocytic leukemia]B Fournier, F Bouscarat, P Le Bozec, et al.
International Journal of Obesity (2005)|June 25, 2014
Is obesity predictive of cardiovascular dysfunction independent of cardiovascular risk factors?E DeVallance, S B Fournier, D A Donley, et al.
British Journal of Haematology|February 1, 1992
Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chainM C Lecomte, H Gautero, O Bournier, et al.
The Journal of General Virology|July 1, 1993
Nucleotide sequence of the bovine viral diarrhoea virus Osloss strain: comparison with related viruses and identification of specific DNA probes in the 5' untranslated regionL De Moerlooze, C Lecomte, S Brown-Shimmer, et al.
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