Results
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143.
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Levamisole adds granulocyte toxicity to 5FU-based chemotherapies in adjuvant treatment of Dukes B-C colorectal cancer. A preliminary report. [electronic resource] by
- Longrée, L
- Focan, C
- Bury, J
- Beauduin, M
- Brohee, D
- Duvivier, A
- Lecomte, M
- Markiewicz, S
- Vindevoghel, A
- Weerts, J
Producer: 19950928
In:
Anticancer research vol. 15
Availability: No items available.
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145.
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Hereditary pyropoikilocytosis and elliptocytosis in a Caucasian family. Transmission of the same molecular defect in spectrin through three generations with different clinical expression. [electronic resource] by
- Lecomte, M C
- Dhermy, D
- Garbarz, M
- Feo, C
- Gautero, H
- Bournier, O
- Picat, C
- Chaveroche, I
- Galand, C
- Boivin, P
Producer: 19880204
In:
Human genetics vol. 77
Availability: No items available.
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146.
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Pathologic and nonpathologic variants of the spectrin molecule in two black families with hereditary elliptocytosis. [electronic resource] by
- Lecomte, M C
- Dhermy, D
- Garbarz, M
- Feo, C
- Gautero, H
- Bournier, O
- Picat, C
- Chaveroche, I
- Ester, A
- Galand, C
Producer: 19860129
In:
Human genetics vol. 71
Availability: No items available.
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147.
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Sp alpha I/78: a mutation of the alpha I spectrin domain in a white kindred with HE and HPP phenotypes. [electronic resource] by
- Lecomte, M C
- Garbarz, M
- Grandchamp, B
- Féo, C
- Gautero, H
- Devaux, I
- Bournier, O
- Galand, C
- d'Auriol, L
- Galibert, F
Producer: 19890907
In:
Blood vol. 74
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148.
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149.
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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 domain. [electronic resource] by
- Garbarz, M
- Lecomte, M C
- Féo, C
- Devaux, I
- Picat, C
- Lefebvre, C
- Galibert, F
- Gautero, H
- Bournier, O
- Galand, C
Producer: 19900525
In:
Blood vol. 75
Availability: No items available.
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150.
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Spectrin beta-chain variant associated with hereditary elliptocytosis. [electronic resource] by
- Dhermy, D
- Lecomte, M C
- Garbarz, M
- Bournier, O
- Galand, C
- Gautero, H
- Feo, C
- Alloisio, N
- Delaunay, J
- Boivin, P
Producer: 19821203
In:
The Journal of clinical investigation vol. 70
Availability: No items available.
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151.
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Prenatal diagnosis of hereditary elliptocytosis with molecular defect of spectrin. [electronic resource] by
- Dhermy, D
- Feo, C
- Garbarz, M
- Lecomte, M C
- Bournier, O
- Chaveroche, I
- Gautero, H
- Boivin, P
- Daffos, F
- Forestier, F
Producer: 19871130
In:
Prenatal diagnosis vol. 7
Availability: No items available.
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152.
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Double inheritance of an alpha I/65 spectrin variant in a child with homozygous elliptocytosis. [electronic resource] by
- Garbarz, M
- Lecomte, M C
- Dhermy, D
- Feo, C
- Chaveroche, I
- Gautero, H
- Bournier, O
- Picat, C
- Goepp, A
- Boivin, P
Producer: 19860703
In:
Blood vol. 67
Availability: No items available.
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153.
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Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia. [electronic resource] by
- Dhermy, D
- Lecomte, M C
- Garbarz, M
- Feo, C
- Gautero, H
- Bournier, O
- Galand, C
- Herrera, A
- Gretillat, F
- Boivin, P
Producer: 19841218
In:
Pediatric research vol. 18
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154.
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155.
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Elliptocytosis-associated spectrin Rouen (beta 220/218) has a truncated but still phosphorylatable beta chain. [electronic resource] by
- Lecomte, M C
- Gautero, H
- Bournier, O
- Galand, C
- Lahary, A
- Vannier, J P
- Garbarz, M
- Delaunay, J
- Tchernia, G
- Boivin, P
Producer: 19920427
In:
British journal of haematology vol. 80
Availability: No items available.
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156.
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Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis. [electronic resource] by
- Pothier, B
- Morlé, L
- Alloisio, N
- Ducluzeau, M T
- Caldani, C
- Féo, C
- Garbarz, M
- Chaveroche, I
- Dhermy, D
- Lecomte, M C
Producer: 19870707
In:
Blood vol. 69
Availability: No items available.
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157.
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Proximal giant neurofilamentous axonopathy in mice genetically engineered to resist calpain and caspase cleavage of α-II spectrin. [electronic resource] by
- Kassa, R
- Monterroso, V
- Wentzell, J
- Ramos, A L
- Couchi, E
- Lecomte, M C
- Iordanov, M
- Kretzschmar, D
- Nicolas, G
- Tshala-Katumbay, D
Producer: 20130411
In:
Journal of molecular neuroscience : MN vol. 47
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158.
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Impact of various emulsifiers on ALA bioavailability and chylomicron synthesis through changes in gastrointestinal lipolysis. [electronic resource] by
- Couëdelo, L
- Amara, S
- Lecomte, M
- Meugnier, E
- Monteil, J
- Fonseca, L
- Pineau, G
- Cansell, M
- Carrière, F
- Michalski, M C
- Vaysse, C
Producer: 20160205
In:
Food & function vol. 6
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159.
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Deletion of the 5'-ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia-positive chronic myeloid leukaemia patients. [electronic resource] by
- Herens, C
- Tassin, F
- Lemaire, V
- Beguin, Y
- Collard, E
- Lampertz, S
- Croisiau, C
- Lecomte, M
- De Prijk, B
- Longrée, L
- Koulischer, L
Producer: 20000913
In:
British journal of haematology vol. 110
Availability: No items available.
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160.
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[The first step to transfuse man with leukocytes and platelets labeled with radiophosphorus]. [electronic resource] by
- JULLIARD, J
- MAUPIN, B
- LOVERDO, A
- BERNARD, J
- COLVEZ, P
- LECOMTE, M
- DUGAS, J
- ARDRY, R
- HENAFF, F
- PERROT, F
- ROBERT, M P
- THEILLEUX, R
Producer: 20040215
In:
La Presse medicale vol. 60
Availability: No items available.
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