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Results: 1-25 | 26-32
Results: 1-25/32
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
COMBINED EFFECT OF 2 DIFFERENT POLYMORPHIC SEQUENCES WITHIN THE BETA-GLOBIN GENE-CLUSTER ON THE LEVEL OF HBF
Authors: GONCALVES I DUCROCQ R LAVINHA J NOGUEIRA PJ PERES MJ PICANCO I CORREIA E REIS AB SILVA C KRISHNAMOORTHY R ALMEIDA LO
Citation: I. Goncalves et al., COMBINED EFFECT OF 2 DIFFERENT POLYMORPHIC SEQUENCES WITHIN THE BETA-GLOBIN GENE-CLUSTER ON THE LEVEL OF HBF, American journal of hematology, 57(4), 1998, pp. 269-276
NEW METHOD FOR QUANTITATIVE-DETERMINATION OF FETAL HEMOGLOBIN-CONTAINING RED-BLOOD-CELLS BY FLOW-CYTOMETRY - APPLICATION TO SICKLE-CELL DISEASE
Authors: NAVENOT JM MERGHOUB T DUCROCQ R MULLER JY KRISHNAMOORTHY R BLANCHARD D
Citation: Jm. Navenot et al., NEW METHOD FOR QUANTITATIVE-DETERMINATION OF FETAL HEMOGLOBIN-CONTAINING RED-BLOOD-CELLS BY FLOW-CYTOMETRY - APPLICATION TO SICKLE-CELL DISEASE, Cytometry, 32(3), 1998, pp. 186-190
UREMIA AND HBA(1C) MEASURED BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY
Authors: CHEVENNE D FONFREDE M DUCROCQ R CHAUFFERT M TRIVIN F
Citation: D. Chevenne et al., UREMIA AND HBA(1C) MEASURED BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Diabetes care, 21(3), 1998, pp. 463-464
NEWBORN SCREENING FOR SICKLE-CELL DISEASE (SCD) - 3 YEARS OF EXPERIENCE FROM PARISIAN AREAS SCREENING-PROGRAM
Authors: BARDAKDJIAN J DUCROCQ R DEMONTALEMBERT M BENKERROU M BERNAUDIN F BRAHIMI L HURTREL D FARRIAUX JP ELION J GALACTEROS F
Citation: J. Bardakdjian et al., NEWBORN SCREENING FOR SICKLE-CELL DISEASE (SCD) - 3 YEARS OF EXPERIENCE FROM PARISIAN AREAS SCREENING-PROGRAM, British Journal of Haematology, 102(1), 1998, pp. 174-174
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
EFFECT OF ALPHA-THALASSEMIA ON SICKLE-CELL-ANEMIA LINKED TO THE ARAB-INDIAN HAPLOTYPE IN INDIA
Authors: MUKHERJEE MB LU CY DUCROCQ R GANGAKHEDKAR RR COLAH RB KADAM MD MOHANTY D NAGEL RL KRISHNAMOORTHY R
Citation: Mb. Mukherjee et al., EFFECT OF ALPHA-THALASSEMIA ON SICKLE-CELL-ANEMIA LINKED TO THE ARAB-INDIAN HAPLOTYPE IN INDIA, American journal of hematology, 55(2), 1997, pp. 104-109
POLYMORPHISM IN EXON-10 OF THE HUMAN COAGULATION-FACTOR-V GENE IN A POPULATION AT RISK FOR SICKLE-CELL DISEASE
Authors: HELLEY D BESMOND C DUCROCQ R DASILVA F GUILLIN MC BEZEAUD A ELION J
Citation: D. Helley et al., POLYMORPHISM IN EXON-10 OF THE HUMAN COAGULATION-FACTOR-V GENE IN A POPULATION AT RISK FOR SICKLE-CELL DISEASE, Human genetics, 100(2), 1997, pp. 245-248
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
INCREASED PROCOAGULANT ACTIVITY OF RED-BLOOD-CELLS FROM PATIENTS WITHHOMOZYGOUS SICKLE-CELL DISEASE AND BETA-THALASSEMIA
Authors: HELLEY D ELDOR A GIROT R DUCROCQ R GUILLIN MC BEZEAUD A
Citation: D. Helley et al., INCREASED PROCOAGULANT ACTIVITY OF RED-BLOOD-CELLS FROM PATIENTS WITHHOMOZYGOUS SICKLE-CELL DISEASE AND BETA-THALASSEMIA, Thrombosis and haemostasis, 76(3), 1996, pp. 322-327
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
PERFUSION CHROMATOGRAPHY ALLOWS AN ORDER OF MAGNITUDE FASTER MEASUREMENT OF THE (G)GAMMA( A)GAMMA RATIO IN PATIENTS WITH AN INCREASED LEVELOF FETAL HEMOGLOBIN/
Authors: WAJCMAN H GALACTEROS F DUCROCQ R
Citation: H. Wajcman et al., PERFUSION CHROMATOGRAPHY ALLOWS AN ORDER OF MAGNITUDE FASTER MEASUREMENT OF THE (G)GAMMA( A)GAMMA RATIO IN PATIENTS WITH AN INCREASED LEVELOF FETAL HEMOGLOBIN/, Blood, 87(4), 1996, pp. 1655-1655
PERFUSION CHROMATOGRAPHY ON REVERSED-PHASE COLUMN ALLOWS FAST ANALYSIS OF HUMAN GLOBIN CHAINS
Authors: WAJCMAN H DUCROCQ R RIOU J MATHIS M GODART C PREHU C GALACTEROS F
Citation: H. Wajcman et al., PERFUSION CHROMATOGRAPHY ON REVERSED-PHASE COLUMN ALLOWS FAST ANALYSIS OF HUMAN GLOBIN CHAINS, Analytical biochemistry, 237(1), 1996, pp. 80-87
HB F-MAURITIUS [(A)GAMMA-23-(B5)-ALA-DELETED] - EVIDENCE FOR AN IDENTICAL HOTSPOT FOR DELETIONS IN THE VARIOUS BETA-LIKE GENES
Authors: WAJCMAN H DUCROCQ R PROME D GALACTEROS F
Citation: H. Wajcman et al., HB F-MAURITIUS [(A)GAMMA-23-(B5)-ALA-DELETED] - EVIDENCE FOR AN IDENTICAL HOTSPOT FOR DELETIONS IN THE VARIOUS BETA-LIKE GENES, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 318(10), 1995, pp. 1065-1071
2 FETAL HEMOGLOBIN-VARIANTS AFFECTING THE SAME RESIDUE - HB F-EMIRATES [(G)GAMMA-59(E3)LYS-]GLU] AND HB F-SACROMONTE [(G)GAMMA-59(E3)LYS-]GLN]
Authors: ABBES S FITZGERALD PA VARADY E GIROT R PIC P BLOUQUIT Y DUCROCQ R DRUPT F WAJCMAN H
Citation: S. Abbes et al., 2 FETAL HEMOGLOBIN-VARIANTS AFFECTING THE SAME RESIDUE - HB F-EMIRATES [(G)GAMMA-59(E3)LYS-]GLU] AND HB F-SACROMONTE [(G)GAMMA-59(E3)LYS-]GLN], Hemoglobin, 19(3-4), 1995, pp. 173-182
ABNORMAL-HEMOGLOBINS IN MAURITIUS ISLAND
Authors: KOTEA N DUCROCQ R SURRUN SK RAMASWAMY R SHUN NK JANKEE S YAN SLK BEESOON S LABIE D KRISHNAMOORTHY R NAGEL RL BALIGADOO S
Citation: N. Kotea et al., ABNORMAL-HEMOGLOBINS IN MAURITIUS ISLAND, American journal of hematology, 48(4), 1995, pp. 293-295
A NEW ALPHA-CHAIN VARIANT HB SALLANCHES [ALPHA-2 104(G11) CYS-]TYR] ASSOCIATED WITH HBH DISEASE IN ONE HOMOZYGOUS PATIENT
Authors: MORLE F FRANCINA A DUCROCQ R WAJCMAN H GONNET C PHILIPPE N SOUILLET G GODBY J
Citation: F. Morle et al., A NEW ALPHA-CHAIN VARIANT HB SALLANCHES [ALPHA-2 104(G11) CYS-]TYR] ASSOCIATED WITH HBH DISEASE IN ONE HOMOZYGOUS PATIENT, British Journal of Haematology, 91(3), 1995, pp. 608-611
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
INFLUENCE OF IRON-DEFICIENCY ON FETAL HEMOGLOBIN EXPRESSION IN CHILDREN WITH SICKLE-CELL DISEASE
Authors: BELLOY M DUCROCQ R DASILVA F BRAHIMI L VILMER E ELION J
Citation: M. Belloy et al., INFLUENCE OF IRON-DEFICIENCY ON FETAL HEMOGLOBIN EXPRESSION IN CHILDREN WITH SICKLE-CELL DISEASE, Blood, 86(10), 1995, pp. 2555-2555
BICENTRIC ORIGIN OF SICKLE HEMOGLOBIN AMONG THE INHABITANTS OF MAURITIUS ISLAND
Authors: KOTEA N BALIGADOO S SURRUN SK RAMASAWMY R LU CY DUCROCQ R LABIE D KRISHNAMOORTHY R NAGEL RL
Citation: N. Kotea et al., BICENTRIC ORIGIN OF SICKLE HEMOGLOBIN AMONG THE INHABITANTS OF MAURITIUS ISLAND, Blood, 86(1), 1995, pp. 407-408
HEMOGLOBINOPATHIES IN THE DOGON COUNTRY - PRESENCE OF BETA(S), BETA(C) AND DELTA(A') GENES
Authors: DUCROCQ R BENNANI M BELLIS G BABY M TRAORE K NAGEL RL KRISHNAMOORTHY R CHAVENTRE A
Citation: R. Ducrocq et al., HEMOGLOBINOPATHIES IN THE DOGON COUNTRY - PRESENCE OF BETA(S), BETA(C) AND DELTA(A') GENES, American journal of hematology, 46(3), 1994, pp. 245-247
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
Risultati: 1-25 | 26-32