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C Lecomte

Showing results (121-130 of 146) with videos related to

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Blood|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.
Journal of Visceral Surgery|March 14, 2021
Management of abdominal emergencies in adults using telemedicine and artificial intelligenceG Gorincour, O Monneuse, A Ben Cheikh, et al.
The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.
Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, et al.
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.
Pageof 15

Showing results (121-130 of 146) with videos related to

Sort By:
Pageof 15
Blood|April 15, 1990
Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domainM Garbarz, M C Lecomte, C Féo, et al.
Journal of Visceral Surgery|March 14, 2021
Management of abdominal emergencies in adults using telemedicine and artificial intelligenceG Gorincour, O Monneuse, A Ben Cheikh, et al.
The Journal of Clinical Investigation|October 1, 1982
Spectrin beta-chain variant associated with hereditary elliptocytosisD Dhermy, M C Lecomte, M Garbarz, et al.
Blood|August 15, 1989
Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypesM C Lecomte, M Garbarz, B Grandchamp, et al.
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.
Pageof 15