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Results:
1-12
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Results: 12
Authors:
Da Costa, L
Willig, TN
Fixler, J
Mohandas, N
Tchernia, G
Citation: L. Da Costa et al., Diamond-Blackfan Anemia, CURR OP PED, 13(1), 2001, pp. 10-15
Authors:
Gazda, H
Lipton, JM
Willig, TN
Ball, S
Niemeyer, CM
Tchernia, G
Mohandas, N
Daly, MJ
Ploszynska, A
Orfali, KA
Vlachos, A
Glader, BE
Rokicka-Milewska, R
Ohara, A
Baker, D
Pospisilova, D
Webber, A
Viskochil, DH
Nathan, DG
Beggs, AH
Sieff, CA
Citation: H. Gazda et al., Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease, BLOOD, 97(7), 2001, pp. 2145-2150
Authors:
Willig, TN
Breton-Gorius, J
Elbim, C
Mignotte, V
Kaplan, C
Mollicone, R
Pasquier, C
Filipe, A
Mielot, F
Cartron, JP
Gougerot-Pocidalo, MA
Debili, N
Guichard, J
Deommergues, JP
Mohandas, N
Tchernia, G
Citation: Tn. Willig et al., Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes - a new syndrome?, BLOOD, 97(3), 2001, pp. 826-828
Authors:
Parsons, SF
Lee, G
Spring, FA
Willig, TN
Peters, LL
Gimm, JA
Tanner, MJA
Mohandas, N
Anstee, DJ
Chasis, JA
Citation: Sf. Parsons et al., Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha 5 chain-containing human laminin with high affinity, BLOOD, 97(1), 2001, pp. 312-320
Authors:
Willig, TN
Gazda, H
Sieff, CA
Citation: Tn. Willig et al., Diamond-Blackfan anemia, CURR OPIN H, 7(2), 2000, pp. 85-94
Authors:
Draptchinskaia, N
Gustavsson, P
Andersson, B
Pettersson, M
Willig, TN
Dianzani, I
Ball, S
Tchernia, G
Klar, J
Matsson, H
Tentler, D
Mohandas, N
Carlsson, B
Dahl, N
Citation: N. Draptchinskaia et al., The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia, NAT GENET, 21(2), 1999, pp. 169-175
Authors:
Willig, TN
Tchernia, G
Citation: Tn. Willig et G. Tchernia, Mutation in the gene encoding ribosomal protein S19 involved in Diamond-Blackfan anaemia, M S-MED SCI, 15(3), 1999, pp. 435-435
Authors:
Tchernia, G
Willig, TN
Citation: G. Tchernia et Tn. Willig, Dyskerin: a new link between ribosomal protein and hematopoiesis?, M S-MED SCI, 15(12), 1999, pp. 1467-1467
Authors:
Willig, TN
Croisille, L
Tchernia, G
Citation: Tn. Willig et al., Diamond-Blackfan syndrome or congenital pure red cell anemia., ANN PEDIAT, 46(1), 1999, pp. 73-80
Authors:
Willig, TN
Niemeyer, CM
Leblanc, T
Tiemann, C
Robert, A
Budde, J
Lambiliotte, A
Kohne, E
Souillet, G
Eber, S
Stephan, JL
Girot, R
Bordigoni, P
Cornu, G
Blanche, S
Guillard, JM
Mohandas, N
Tchernia, G
Citation: Tn. Willig et al., Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients, PEDIAT RES, 46(5), 1999, pp. 553-561
Authors:
Willig, TN
Draptchinskaia, N
Dianzani, I
Ball, S
Niemeyer, C
Ramenghi, U
Orfali, K
Gustavsson, P
Garelli, E
Brusco, A
Tiemann, C
Perignon, JL
Bouchier, C
Cicchiello, L
Dahl, N
Mohandas, N
Tchernia, G
Citation: Tn. Willig et al., Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: Wide variations in phenotypic expression, BLOOD, 94(12), 1999, pp. 4294-4306
Authors:
Willig, TN
Ball, SE
Tchernia, G
Citation: Tn. Willig et al., Diamond-Blackfan anaemia: current concepts and issues, GEMATOL TR, 43(3), 1998, pp. 15-18
Risultati:
1-12
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