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Results: 1-18 |
Results: 18
MYELODYSPLASTIC SYNDROMES IN CHILDHOOD - IS THE FAB CLASSIFICATION RELEVANT - REPORT OF 81 CHILDREN FROM A FRENCH MULTICENTER STUDY
Authors: MIELOT F BUISINE J DUCHAYNE E FENNETEAU O GOASGUEN J GUITARD AM MAIERREDELSPERGER M MALET M MANEL AM
Citation: F. Mielot et al., MYELODYSPLASTIC SYNDROMES IN CHILDHOOD - IS THE FAB CLASSIFICATION RELEVANT - REPORT OF 81 CHILDREN FROM A FRENCH MULTICENTER STUDY, Leukemia & lymphoma, 28(5-6), 1998, pp. 531
COMPOUND HETEROZYGOSITY HB-S HB HOPE (BETA(136)GLY-]ASP) - A PITFALL IN THE NEWBORN SCREENING FOR SICKLE-CELL DISEASE
Authors: DUCROCQ R BEVIER A LENEVEU A MAIERREDELSPERGER M BARDAKDJIANMICHAU J BADENS C ELION J
Citation: R. Ducrocq et al., COMPOUND HETEROZYGOSITY HB-S HB HOPE (BETA(136)GLY-]ASP) - A PITFALL IN THE NEWBORN SCREENING FOR SICKLE-CELL DISEASE, Journal of medical screening, 5(1), 1998, pp. 27-30
HB GODAVARI [ALPHA-95(G2)PRO-]THR] - A NEUTRAL AMINO-ACID SUBSTITUTION IN THE ALPHA-1-BETA-2 INTERFACE THAT MODIFIES THE ELECTROPHORETIC MOBILITY OF HEMOGLOBIN
Authors: WAJCMAN H KISTER J RIOU J GALACTEROS F GIROT R MAIERREDELSPERGER M NAYUDU NVS GIORDANO PC
Citation: H. Wajcman et al., HB GODAVARI [ALPHA-95(G2)PRO-]THR] - A NEUTRAL AMINO-ACID SUBSTITUTION IN THE ALPHA-1-BETA-2 INTERFACE THAT MODIFIES THE ELECTROPHORETIC MOBILITY OF HEMOGLOBIN, Hemoglobin, 22(1), 1998, pp. 11-22
FETAL HEMOGLOBIN AND F-CELL RESPONSES TO LONG-TERM HYDROXYUREA TREATMENT IN YOUNG SICKLE-CELL PATIENTS
Authors: MAIERREDELSPERGER M DEMONTALEMBERT M FLAHAULT A NEONATO MG DUCROCQ R MASSON MP GIROT R ELION J
Citation: M. Maierredelsperger et al., FETAL HEMOGLOBIN AND F-CELL RESPONSES TO LONG-TERM HYDROXYUREA TREATMENT IN YOUNG SICKLE-CELL PATIENTS, Blood, 91(12), 1998, pp. 4472-4479
3-YEAR FOLLOW-UP OF HYDROXYUREA TREATMENT IN SEVERELY ILL CHILDREN WITH SICKLE-CELL DISEASE
Authors: DEMONTALEMBERT M BELLOY M BERNAUDIN F GOURAUD F CAPDEVILLE R MARDINI R PHILIPPE N JAIS JP BARDAKDJIAN J DUCROCQ R MAIERREDELSPERGER M ELION J LABIE D GIROT R
Citation: M. Demontalembert et al., 3-YEAR FOLLOW-UP OF HYDROXYUREA TREATMENT IN SEVERELY ILL CHILDREN WITH SICKLE-CELL DISEASE, Journal of pediatric hematology/oncology, 19(4), 1997, pp. 313-318
DISSECTION OF THE ASSOCIATION STATUS OF 2 POLYMORPHISMS IN THE BETA-GLOBIN GENE-CLUSTER WITH VARIATIONS IN F-CELL NUMBER IN NONANEMIC INDIVIDUALS
Authors: MERGHOUB T PERICHON B MAIERREDELSPERGER M DIBENEDETTO SP SAMPERI P DUCROCQ R FEINGOLD N ELION J SCHILIRO G LABIE D KRISHNAMOORTHY R
Citation: T. Merghoub et al., DISSECTION OF THE ASSOCIATION STATUS OF 2 POLYMORPHISMS IN THE BETA-GLOBIN GENE-CLUSTER WITH VARIATIONS IN F-CELL NUMBER IN NONANEMIC INDIVIDUALS, American journal of hematology, 56(4), 1997, pp. 239-243
SEA-BLUE HISTIOCYTES IN BONE-MARROW DUE TO A LONG-TERM TOTAL PARENTERAL-NUTRITION INCLUDING FAT-EMULSIONS
Authors: MAIERREDELSPERGER M GIROT R
Citation: M. Maierredelsperger et R. Girot, SEA-BLUE HISTIOCYTES IN BONE-MARROW DUE TO A LONG-TERM TOTAL PARENTERAL-NUTRITION INCLUDING FAT-EMULSIONS, British Journal of Haematology, 97(3), 1997, pp. 689-689
THE RELATIVE IMPORTANCE OF THE X-LINKED FCP LOCUS AND BETA-GLOBIN HAPLOTYPES IN DETERMINING HEMOGLOBIN-F LEVELS - A STUDY OF SS-PATIENTS HOMOZYGOUS FOR BETA(S)-HAPLOTYPES
Authors: CHANG YPC MAIERREDELSPERGER M SMITH KD CONTU L DUCROCQ R DEMONTALEMBERT M BELLOY M ELION J DOVER GJ GIROT R
Citation: Ypc. Chang et al., THE RELATIVE IMPORTANCE OF THE X-LINKED FCP LOCUS AND BETA-GLOBIN HAPLOTYPES IN DETERMINING HEMOGLOBIN-F LEVELS - A STUDY OF SS-PATIENTS HOMOZYGOUS FOR BETA(S)-HAPLOTYPES, British Journal of Haematology, 96(4), 1997, pp. 806-814
INFLUENCE OF HEMOGLOBIN LEVEL REDUCTION AND IRON-DEFICIENCY ON SICKLE-CELL CRISES
Authors: GIROT R RAPHALEN P BUKSERERO A MANIGNE P KANFER A DEMONTALEMBERT M MAIERREDELSPERGER M
Citation: R. Girot et al., INFLUENCE OF HEMOGLOBIN LEVEL REDUCTION AND IRON-DEFICIENCY ON SICKLE-CELL CRISES, Blood, 88(10), 1996, pp. 45-45
VARIATION OF FETAL HEMOGLOBIN AND F-CELL NUMBER WITH THE LCR-HS2 POLYMORPHISM IN NONANEMIC INDIVIDUALS
Authors: MERGHOUB T MAIERREDELSPERGER M LABIE D FEINGOLD N DIBENEDETTO SP SAMPERI P SCHILIRO G DUCROCQ R ELION J KRISHNAMOORTHY R
Citation: T. Merghoub et al., VARIATION OF FETAL HEMOGLOBIN AND F-CELL NUMBER WITH THE LCR-HS2 POLYMORPHISM IN NONANEMIC INDIVIDUALS, Blood, 87(6), 1996, pp. 2607-2609
THE RELATIVE IMPORTANCE OF THE X-LINKED FCP LOCUS AND BETA-GLOBIN HAPLOTYPES IN DETERMINING HEMOGLOBIN-F LEVELS - A STUDY OF SS PATIENTS HOMOZYGOUS FOR BETA(S) HAPLOTYPES
Authors: CHANG Y MAIERREDELSPERGER M DOVER G SMITH K CONTU L ELION J DUCROCQ R DEMONTALEMBERT M GIROT R BELLORY M
Citation: Y. Chang et al., THE RELATIVE IMPORTANCE OF THE X-LINKED FCP LOCUS AND BETA-GLOBIN HAPLOTYPES IN DETERMINING HEMOGLOBIN-F LEVELS - A STUDY OF SS PATIENTS HOMOZYGOUS FOR BETA(S) HAPLOTYPES, Blood, 86(10), 1995, pp. 1658-1658
THE USE OF STAPHYLOCOCCUS V8 PROTEASE IN THE STRUCTURAL DETERMINATIONOF HUMAN HEMOGLOBIN-VARIANTS - HB VALPARAISO [ALPHA-88(F9)ALA-]GLY] AS EXAMPLE
Authors: WAJCMAN H DEMONTALEMBERT M GIROT R KISTER J MAIERREDELSPERGER M GALACTEROS F
Citation: H. Wajcman et al., THE USE OF STAPHYLOCOCCUS V8 PROTEASE IN THE STRUCTURAL DETERMINATIONOF HUMAN HEMOGLOBIN-VARIANTS - HB VALPARAISO [ALPHA-88(F9)ALA-]GLY] AS EXAMPLE, Hemoglobin, 18(4-5), 1994, pp. 275-284
FETAL HEMOGLOBIN VARIATIONS FOLLOWING HYDROXYUREA TREATMENT IN PATIENTS WITH CYANOTIC CONGENITAL HEART-DISEASE
Authors: TRIADOU P MAIERREDELSPERGER M KRISHNAMOORTY R DESCHAMPS A CASADEVALL N DUNDA O DUCROCQ R ELION J GIROT R LABIE D DOVER G CORNU P
Citation: P. Triadou et al., FETAL HEMOGLOBIN VARIATIONS FOLLOWING HYDROXYUREA TREATMENT IN PATIENTS WITH CYANOTIC CONGENITAL HEART-DISEASE, Nouvelle revue francaise d'hematologie, 36(5), 1994, pp. 367-372
VARIATION IN FETAL HEMOGLOBIN PARAMETERS AND PREDICTED HEMOGLOBIN-S POLYMERIZATION IN SICKLE-CELL CHILDREN IN THE FIRST 2 YEARS OF LIFE - PARISIAN PROSPECTIVE-STUDY ON SICKLE-CELL DISEASE
Authors: MAIERREDELSPERGER M NOGUCHI CT DEMONTALEMBERT M RODGERS GP SCHECHTER AN GOURBIL A BLANCHARD D JAIS JP DUCROCQ R PELTIER JY COTTAT MC LACAILLE F BELLOY M ELION J LABIE D GIROT R
Citation: M. Maierredelsperger et al., VARIATION IN FETAL HEMOGLOBIN PARAMETERS AND PREDICTED HEMOGLOBIN-S POLYMERIZATION IN SICKLE-CELL CHILDREN IN THE FIRST 2 YEARS OF LIFE - PARISIAN PROSPECTIVE-STUDY ON SICKLE-CELL DISEASE, Blood, 84(9), 1994, pp. 3182-3188
VARIATION IN FETAL HEMOGLOBIN PARAMETERS AND PREDICTED HEMOGLOBIN-S POLYMERIZATION IN SICKLE-CELL CHILDREN IN THE FIRST 2 YEARS OF LIFE - PARISIAN PROSPECTIVE-STUDY ON SICKLE-CELL DISEASE
Authors: MAIERREDELSPERGER M NOGUCHI CT DEMONTALEMBERT M RODGERS GP SCHECHTER AN GOURBIL A BLANCHARD D JAIS JP DUCROCQ R PELTIER JY COTTAT MC LACAILLE F BELLOY M ELION J LABIE D GIROT R
Citation: M. Maierredelsperger et al., VARIATION IN FETAL HEMOGLOBIN PARAMETERS AND PREDICTED HEMOGLOBIN-S POLYMERIZATION IN SICKLE-CELL CHILDREN IN THE FIRST 2 YEARS OF LIFE - PARISIAN PROSPECTIVE-STUDY ON SICKLE-CELL DISEASE, Blood, 84(9), 1994, pp. 3182-3188
CLINICAL AND HEMATOLOGICAL RESPONSE OF SICKLE-CELL CHILDREN TO TREATMENT WITH HYDROXYUREA
Authors: DEMONTALEMBERT M BELLOY M BERNAUDIN F DUCROCQ R MAIERREDELSPERGER M PHILIPPE N SCHECHTER A GIROT R
Citation: M. Demontalembert et al., CLINICAL AND HEMATOLOGICAL RESPONSE OF SICKLE-CELL CHILDREN TO TREATMENT WITH HYDROXYUREA, Blood, 84(10), 1994, pp. 10000219-10000219
CELLULAR-PARAMETERS OF FETAL HEMOGLOBIN RESPONSE AND PREDICTED HEMOGLOBIN S POLYMERIZATION IN SICKLE-CELL CHILDREN TREATED WITH HYDROXYUREA
Authors: MAIERREDELSPERGER M DEMONTALEMBERT M NOGUCHI CT DUCROCQ R BARDAKDJIAN J BELLOY M BERNAUDIN F PHILLIPPE N ELION J SCHECHTER AN GIROT R
Citation: M. Maierredelsperger et al., CELLULAR-PARAMETERS OF FETAL HEMOGLOBIN RESPONSE AND PREDICTED HEMOGLOBIN S POLYMERIZATION IN SICKLE-CELL CHILDREN TREATED WITH HYDROXYUREA, Blood, 84(10), 1994, pp. 10000414-10000414
BETA-GLOBIN GENE-CLUSTER HAPLOTYPE AND ALPHA-THALASSEMIA DO NOT CORRELATE WITH THE ACUTE CLINICAL MANIFESTATIONS OF SICKLE-CELL DISEASE IN CHILDREN
Authors: DEMONTALEMBERT M MAIERREDELSPERGER M GIROT R BELLOY M VILMER E DUCROCQ R GUIDAL C ELION J
Citation: M. Demontalembert et al., BETA-GLOBIN GENE-CLUSTER HAPLOTYPE AND ALPHA-THALASSEMIA DO NOT CORRELATE WITH THE ACUTE CLINICAL MANIFESTATIONS OF SICKLE-CELL DISEASE IN CHILDREN, Blood, 82(8), 1993, pp. 2595-2596
Risultati: 1-18 |