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Results: 1-23 |
Results: 23
Novel C-60-based building blocks derived from C-60(2-) anion
Authors: Allard, E Delaunay, J Cheng, FY Cousseau, J Orduna, J Garin, J
Citation: E. Allard et al., Novel C-60-based building blocks derived from C-60(2-) anion, ORG LETT, 3(22), 2001, pp. 3503-3506
Heimiol A, a new dimeric stilbenoid from Neobalanocarpus heimii
Authors: Weber, JFF Wahab, IA Marzuki, A Thomas, NF Kadir, AA Hadi, AHA Awang, K Latiff, AA Richomme, P Delaunay, J
Citation: Jff. Weber et al., Heimiol A, a new dimeric stilbenoid from Neobalanocarpus heimii, TETRAHEDR L, 42(29), 2001, pp. 4895-4897
The dumbbell his Diels-Alder adduct between tetramethylidene[4H]tetrathiafulvalene and two C-60
Authors: Liu, SG Kreher, D Hudhomme, P Levillain, E Cariou, M Delaunay, J Gorgues, A Vidal-Gancedo, J Veciana, J Rovira, C
Citation: Sg. Liu et al., The dumbbell his Diels-Alder adduct between tetramethylidene[4H]tetrathiafulvalene and two C-60, TETRAHEDR L, 42(22), 2001, pp. 3717-3720
Natural history of congenital dyserythropoietic anemia type II
Authors: Iolascon, A Delaunay, J Wickramasinghe, SN Perrotta, S Gigante, M Camaschella, C
Citation: A. Iolascon et al., Natural history of congenital dyserythropoietic anemia type II, BLOOD, 98(4), 2001, pp. 1258-1260
Serum sICAM-1 (soluble intercellular adhesion molecule-1) and M-CSF (macrophage colony-stimulating growth factor) throughout monitoring of 34 non-serous ovarian cancers
Authors: Callet, N Delaunay, J Pichon, MF
Citation: N. Callet et al., Serum sICAM-1 (soluble intercellular adhesion molecule-1) and M-CSF (macrophage colony-stimulating growth factor) throughout monitoring of 34 non-serous ovarian cancers, EUR J GYN O, 21(2), 2000, pp. 135-140
Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?
Authors: Iolascon, A Servedio, V Carbone, R Totaro, A Carella, M Perrotta, S Wickramasinghe, SN Delaunay, J Heimpel, H Gasparini, P
Citation: A. Iolascon et al., Geographic distribution of CDA-II: did a founder effect operate in Southern Italy?, HAEMATOLOG, 85(5), 2000, pp. 470-474
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4.2(-) hereditary spherocytosis (949delG)
Authors: Beauchamp-Nicoud, A Morle, L Lutz, HU Stammler, P Agulles, O Petermann-Khder, R Iolascon, A Perrotta, S Cynober, T Tchernia, G Delaunay, J Baudin-Creuza, V
Citation: A. Beauchamp-nicoud et al., Heavy transfusions and presence of an anti-protein 4.2 antibody in 4.2(-) hereditary spherocytosis (949delG), HAEMATOLOG, 85(1), 2000, pp. 19-24
Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapy
Authors: Parez, N Dommergues, M Zupan, V Chambost, ZH Fieschi, JB Delaunay, J Mielot, F Cramer, EM Dommergues, JP Wickramasinghe, SN Tchernia, G
Citation: N. Parez et al., Severe congenital dyserythropoietic anaemia type I: prenatal management, transfusion support and alpha-interferon therapy, BR J HAEM, 110(2), 2000, pp. 420-423
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24
Authors: Grootenboer, S Schischmanoff, PO Laurendeau, I Cynober, T Tchernia, G Dommergues, JP Dhermy, D Bost, M Varet, B Snyder, M Ballas, SK Ducot, B Babron, MC Stewart, GW Gasparini, P Iolascon, A Delaunay, J
Citation: S. Grootenboer et al., Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24, BLOOD, 96(7), 2000, pp. 2599-2605
Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3
Authors: Ribeiro, ML Alloisio, N Almeida, H Gomes, C Texier, P Lemos, C Mimoso, G Morle, L Bey-Cabet, F Rudigoz, RC Delaunay, J Tamagnini, G
Citation: Ml. Ribeiro et al., Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3, BLOOD, 96(4), 2000, pp. 1602-1604
Elliptocytosis in patients with C-terminal domain mutations of protein 4.1correlates with encoded messenger RNA levels rather than with alterations in primary protein structure
Authors: Moriniere, M Ribeiro, L Dalla Venezia, N Deguillien, M Maillet, P Cynober, T Delhommeau, F Almeida, H Tamagnini, G Delaunay, J Baklouti, F
Citation: M. Moriniere et al., Elliptocytosis in patients with C-terminal domain mutations of protein 4.1correlates with encoded messenger RNA levels rather than with alterations in primary protein structure, BLOOD, 95(5), 2000, pp. 1834-1841
Natural history of hereditary spherocytosis during the first year of life
Authors: Delhommeau, F Cynober, T Schischmanoff, PO Rohrlich, P Delaunay, J Mohandas, N Tchernia, G
Citation: F. Delhommeau et al., Natural history of hereditary spherocytosis during the first year of life, BLOOD, 95(2), 2000, pp. 393-397
The congenital dyserythropoietic anaemias
Authors: Delaunay, J Iolascon, A
Citation: J. Delaunay et A. Iolascon, The congenital dyserythropoietic anaemias, BEST P R C, 12(4), 1999, pp. 691-705
A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon
Authors: Maillet, P Dalla Venezia, N Lorenzo, F Moriniere, M Bozon, M Noel, B Delaunay, J Baklouti, F
Citation: P. Maillet et al., A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon, HUM MUTAT, 14(2), 1999, pp. 145-155
Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia
Authors: Carella, M Stewart, GW Ajetunmobi, JF Schettini, F Delaunay, J Iolascon, A
Citation: M. Carella et al., Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia, HAEMATOLOG, 84(9), 1999, pp. 862-863
The frequency of allele alpha(LELY), a low expression allele of the gene encoding erythroid spectrin alpha-chain, in the Greek population
Authors: Papassideri, I Antonelou, M Karababa, F Loutradi-Anagnostou, A Delaunay, J Margaritis, LH
Citation: I. Papassideri et al., The frequency of allele alpha(LELY), a low expression allele of the gene encoding erythroid spectrin alpha-chain, in the Greek population, HAEMATOLOG, 84(8), 1999, pp. 754-755
Southeast Asian ovalocytosis in white persons
Authors: Schischmanoff, PO Cynober, T Mielot, F Leclerc, L Vasseur-Godbillon, C Baudin-Creuza, V Magowan, C Yeung, J Mohandas, N Tchernia, G Delaunay, J
Citation: Po. Schischmanoff et al., Southeast Asian ovalocytosis in white persons, HEMOGLOBIN, 23(1), 1999, pp. 47-56
Recognizing types I, II and III congenital dyserythropoietic anemias now that the causative genes have been identified.
Authors: Delaunay, J
Citation: J. Delaunay, Recognizing types I, II and III congenital dyserythropoietic anemias now that the causative genes have been identified., ANN PEDIAT, 46(1), 1999, pp. 64-72
Chemical generation and reactivity of C-60(2-). High-yield and regioselective alkylation of [60, I-h] fullerene
Authors: Allard, E Riviere, L Delaunay, J Dubois, D Cousseau, J
Citation: E. Allard et al., Chemical generation and reactivity of C-60(2-). High-yield and regioselective alkylation of [60, I-h] fullerene, TETRAHEDR L, 40(40), 1999, pp. 7223-7226
Suppression of CDA II expression in a homozygote
Authors: Beauchamp-Nicoud, A Schischmanoff, PO Alloisio, N Boivin, P Parsons, SF Mielot, F Tchernia, G Legrand, A del Giudice, EM Gasparini, P Iolascon, A Wickramasinghe, SN Delaunay, J
Citation: A. Beauchamp-nicoud et al., Suppression of CDA II expression in a homozygote, BR J HAEM, 106(4), 1999, pp. 948-953
Mutation at position -12 of intron 45 (c -> t) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele alpha(LELY) inerythroid cells
Authors: Wilmotte, R Marechal, J Delaunay, J
Citation: R. Wilmotte et al., Mutation at position -12 of intron 45 (c -> t) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele alpha(LELY) inerythroid cells, BR J HAEM, 104(4), 1999, pp. 855-859
Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis)
Authors: Iolascon, A Stewart, GW Ajetunmobi, JF Perrotta, S Delaunay, J Carella, M Zelante, L Gasparini, P
Citation: A. Iolascon et al., Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis), BLOOD, 93(9), 1999, pp. 3120-3123
Synthesis and X-ray crystal structure of 1,2-dichloro-1,2-bis(phenyltellanyl)ethylene
Authors: Le Guillanton, G Martynov, AV Delaunay, J Mercier, N Riou, A
Citation: G. Le Guillanton et al., Synthesis and X-ray crystal structure of 1,2-dichloro-1,2-bis(phenyltellanyl)ethylene, J CHEM R-S, (11), 1998, pp. 681-681A
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