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Results: 1-25 | 26-50 | 51-75 | 76-85
Results: 1-25/85
ABNORMALITIES OF THE ADULT SHOULDER DUE TO SICKLE-CELL OSTEONECROSIS DURING CHILDHOOD
Authors: HERNIGOU P ALLAIN J BACHIR D GALACTEROS F
Citation: P. Hernigou et al., ABNORMALITIES OF THE ADULT SHOULDER DUE TO SICKLE-CELL OSTEONECROSIS DURING CHILDHOOD, Revue du rhumatisme, 65(1), 1998, pp. 27-32
HEMOGLOBIN PHNOM PEHN [ALPHA-117PHE(H1)-ILE-ALPHA-118THR(H2)] - EVIDENCE FOR A HOTSPOT FOR INSERTION OF RESIDUES IN THE 3RD EXON OF THE ALPHA-1-GLOBIN GENE
Authors: WAJCMAN H PREHU MO PREHU C BLOUQUIT Y PROME D GALACTEROS F
Citation: H. Wajcman et al., HEMOGLOBIN PHNOM PEHN [ALPHA-117PHE(H1)-ILE-ALPHA-118THR(H2)] - EVIDENCE FOR A HOTSPOT FOR INSERTION OF RESIDUES IN THE 3RD EXON OF THE ALPHA-1-GLOBIN GENE, Human mutation, 1998, pp. 20-22
ABNORMAL VENOARTERIAL REFLEX (VAR) IN HOMOZYGOUS SICKLE-CELL DISEASE
Authors: BACHIR D MAUREL A GALACTEROS F
Citation: D. Bachir et al., ABNORMAL VENOARTERIAL REFLEX (VAR) IN HOMOZYGOUS SICKLE-CELL DISEASE, Journal of vascular research, 35, 1998, pp. 246-246
HB LES-ANDELYS [ALPHA-83(F4)LEU-]PRO] - A NEW MODERATELY UNSTABLE VARIANT
Authors: WAJCMAN H PROME D PREHU C DEON C RIOU J BOUANGA JC PAPASSOTIRIOU I LAHARY A GALACTEROS F
Citation: H. Wajcman et al., HB LES-ANDELYS [ALPHA-83(F4)LEU-]PRO] - A NEW MODERATELY UNSTABLE VARIANT, Hemoglobin, 22(2), 1998, pp. 129-140
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
HEMOGLOBINS IN TOGOLESE NEWBORNS - HB-S, HB-C, HB-BARTS, AND ALPHA-GLOBIN GENE STATUS
Authors: SEGBENA AY PREHU C WAJCMAN H BARDAKDJIANMICHAU J MESSIE K FETEKE L VOVOR A DAVID M FEINGOLD J GALACTEROS F
Citation: Ay. Segbena et al., HEMOGLOBINS IN TOGOLESE NEWBORNS - HB-S, HB-C, HB-BARTS, AND ALPHA-GLOBIN GENE STATUS, American journal of hematology, 59(3), 1998, pp. 208-213
GENETIC AND HEMATOLOGICAL STUDIES IN A GROUP OF 114 ADULT PATIENTS WITH SC SICKLE-CELL DISEASE
Authors: LEE K PREHU C MERAULT G KECLARD L ROUDOTTHORAVAL F BACHIR D WAJCMAN H DENIS L GALACTEROS F
Citation: K. Lee et al., GENETIC AND HEMATOLOGICAL STUDIES IN A GROUP OF 114 ADULT PATIENTS WITH SC SICKLE-CELL DISEASE, American journal of hematology, 59(1), 1998, pp. 15-21
EARLY GLOMERULAR DYSFUNCTION IN PATIENTS WITH SICKLE-CELL-ANEMIA
Authors: SCHMITT F MARTINEZ F BRILLET G GIATRAS I CHOUKROUN G GIROT R BACHIR D GALACTEROS F LACOUR B GRUNFELD JP
Citation: F. Schmitt et al., EARLY GLOMERULAR DYSFUNCTION IN PATIENTS WITH SICKLE-CELL-ANEMIA, American journal of kidney diseases, 32(2), 1998, pp. 208-214
THE LUTHERAN BLOOD-GROUP GLYCOPROTEINS, THE ERYTHROID RECEPTORS FOR LAMININ, ARE ADHESION MOLECULES
Authors: ELNEMER W GANE P COLIN Y BONY V RAHUEL C GALACTEROS F CARTRON JP LEVANKIM C
Citation: W. Elnemer et al., THE LUTHERAN BLOOD-GROUP GLYCOPROTEINS, THE ERYTHROID RECEPTORS FOR LAMININ, ARE ADHESION MOLECULES, The Journal of biological chemistry, 273(27), 1998, pp. 16686-16693
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
HB MONT-SAINT-AIGNAN [BETA-128 (H6) ALA-]PRO] - A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA
Authors: WAJCMAN H LAHARY A RIOU J GODART C PREHU C PROME D GALACTEROS F
Citation: H. Wajcman et al., HB MONT-SAINT-AIGNAN [BETA-128 (H6) ALA-]PRO] - A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA, British Journal of Haematology, 102(1), 1998, pp. 177-177
HB MONTFERMEIL [BETA130(H8) TYR-]CYS] - A NEW HEMOGLOBIN-VARIANT WITHINCREASED OXYGEN-AFFINITY - COMPARISON WITH 2 RECOMBINANT HEMOGLOBINS- HB BETA-Y130A AND HB BETA-Y130F
Authors: KISTER J BAUDINCREUZA V KIGER L PREHU C RIOU J PAGNIER J POYART C PROME D GALACTEROS F WAJCMAN H
Citation: J. Kister et al., HB MONTFERMEIL [BETA130(H8) TYR-]CYS] - A NEW HEMOGLOBIN-VARIANT WITHINCREASED OXYGEN-AFFINITY - COMPARISON WITH 2 RECOMBINANT HEMOGLOBINS- HB BETA-Y130A AND HB BETA-Y130F, British Journal of Haematology, 102(1), 1998, pp. 178-178
MAGNESIUM ORAL SUPPLEMENTS AND HEMOGLOBINOPATHIES
Authors: DEFRANCESCHI L BEUZARD Y GALACTEROS F CAPPELLINI MD BACHIR D PLATT O ALPER SL GRAZIADEL G TCHERNIA J CORROCHER R BRUGNARA C
Citation: L. Defranceschi et al., MAGNESIUM ORAL SUPPLEMENTS AND HEMOGLOBINOPATHIES, British Journal of Haematology, 102(1), 1998, pp. 273-273
HEMOGLOBIN J-BISKRA - A NEW MILDLY UNSTABLE ALPHA-1 GENE VARIANT WITHA DELETION OF 8 RESIDUES (ALPHA-50-57, ALPHA-51-58 OR ALPHA-52-59) INCLUDING THE DISTAL HISTIDINE
Authors: WAJCMAN H DAHMANE M PREHU C COSTES B PROME D AROUS N BARDAKDJIANMICHAU J RIOU J AYACHE KC GODART C GALACTEROS F
Citation: H. Wajcman et al., HEMOGLOBIN J-BISKRA - A NEW MILDLY UNSTABLE ALPHA-1 GENE VARIANT WITHA DELETION OF 8 RESIDUES (ALPHA-50-57, ALPHA-51-58 OR ALPHA-52-59) INCLUDING THE DISTAL HISTIDINE, British Journal of Haematology, 100(2), 1998, pp. 401-406
GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND HOMOZYGOUS SICKLE-CELL DISEASE IN CONGO
Authors: BOUANGA JC MOUELE R PREHU C WAJCMAN H FEINGOLD J GALACTEROS F
Citation: Jc. Bouanga et al., GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND HOMOZYGOUS SICKLE-CELL DISEASE IN CONGO, Human heredity, 48(4), 1998, pp. 192-197
STRUCTURAL AND FUNCTIONAL-STUDIES OF HEMOGLOBIN MOABIT (ALPHA-86(F7))LEU-]ARG
Authors: GULBIS B TSHILOLO L WAJCMAN H RIOU J GALACTEROS F PROME D KISTER J PAPASSOTIRIOU I VANLAETHEM Y VERTONGEN F
Citation: B. Gulbis et al., STRUCTURAL AND FUNCTIONAL-STUDIES OF HEMOGLOBIN MOABIT (ALPHA-86(F7))LEU-]ARG, HEM CELL TH, 39(3), 1997, pp. 137-138
COMBINED MASS-SPECTROMETRIC METHODS FOR THE CHARACTERIZATION OF HUMANHEMOGLOBIN-VARIANTS LOCALIZED WITHIN ALPHA-T9 PEPTIDE - IDENTIFICATION OF HB VILLEURBANNE ALPHA-89 (FG1) HIS-]TYR
Authors: DEON C PROME JC PROME D FRANCINA A GROFF P KALMES G GALACTEROS F WAJCMAN H
Citation: C. Deon et al., COMBINED MASS-SPECTROMETRIC METHODS FOR THE CHARACTERIZATION OF HUMANHEMOGLOBIN-VARIANTS LOCALIZED WITHIN ALPHA-T9 PEPTIDE - IDENTIFICATION OF HB VILLEURBANNE ALPHA-89 (FG1) HIS-]TYR, Journal of mass spectrometry., 32(8), 1997, pp. 880-887
SPLENIC INFARCTION REVEALING SICKLE-CELL TRAIT ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS
Authors: SANTIAGO J BONAIME V CHERAITIA Y ROBERT R GALACTEROS F
Citation: J. Santiago et al., SPLENIC INFARCTION REVEALING SICKLE-CELL TRAIT ASSOCIATED WITH HEREDITARY SPHEROCYTOSIS, Archives de pediatrie, 4(12), 1997, pp. 1262-1263
ALTERATION OF AN INTERSUBUNIT CONTACT IN HEMOGLOBIN-VARIANTS - COMPARATIVE-STUDY OF MODIFICATIONS AT POSITION ALPHA-126 ASP (H9)
Authors: KISTER J GRIFFON N HENTHORN JS MARDEN MC POYART C PAPASSOTIRIOU I PROME D GALACTEROS F DAVIES SC WAJCMAN H
Citation: J. Kister et al., ALTERATION OF AN INTERSUBUNIT CONTACT IN HEMOGLOBIN-VARIANTS - COMPARATIVE-STUDY OF MODIFICATIONS AT POSITION ALPHA-126 ASP (H9), Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 320(11), 1997, pp. 849-855
CHARACTERISTICS OF HEPATITIS-C VIRUS-INFECTION IN PATIENTS WITH SICKLE-CELL DISEASE (SCD) AND INFLUENCE ON LIVER-DISEASE
Authors: BASTIE A BLANC L LEE K BACHIR D GODEAU B ROUDOTTHORAVAL F DARTHUY F REMIRE J GALACTEROS F SCHAEFFER A DHUMEAUX D PAWLOTSKY JM
Citation: A. Bastie et al., CHARACTERISTICS OF HEPATITIS-C VIRUS-INFECTION IN PATIENTS WITH SICKLE-CELL DISEASE (SCD) AND INFLUENCE ON LIVER-DISEASE, Hepatology, 26(4), 1997, pp. 1130-1130
PREVENTIVE AND CURATIVE TREATMENT OF PRIA PISM IN SICKLE-CELL DISEASE
Authors: BACHIR D VIRAG R LEE K BELLOY M DEMONTALEMBERT M DENIS L BROYART A GIROT R GALACTEROS F
Citation: D. Bachir et al., PREVENTIVE AND CURATIVE TREATMENT OF PRIA PISM IN SICKLE-CELL DISEASE, La Revue de medecine interne, 18, 1997, pp. 46-51
ORAL MAGNESIUM SUPPLEMENTS REDUCE ERYTHROCYTE DEHYDRATION IN PATIENTSWITH SICKLE-CELL DISEASE
Authors: DEFRANCESCHI L BACHIR D GALACTEROS F TCHERNIA G CYNOBER T ALPER S PLATT O BEUZARD Y BRUGNARA C
Citation: L. Defranceschi et al., ORAL MAGNESIUM SUPPLEMENTS REDUCE ERYTHROCYTE DEHYDRATION IN PATIENTSWITH SICKLE-CELL DISEASE, The Journal of clinical investigation, 100(7), 1997, pp. 1847-1852
CATION-EXCHANGE HPLC EVALUATED FOR PRESUMPTIVE IDENTIFICATION OF HEMOGLOBIN-VARIANTS
Authors: RIOU J GODART C HURTREL D MATHIS M BIMET C BARDAKDJIANMICHAU J PREHU C WAJCMAN H GALACTEROS F
Citation: J. Riou et al., CATION-EXCHANGE HPLC EVALUATED FOR PRESUMPTIVE IDENTIFICATION OF HEMOGLOBIN-VARIANTS, Clinical chemistry, 43(1), 1997, pp. 34-39
MOLECULAR SCREENING FOR -3.7 KB DELETIONNAL ALPHA-THALASSEMIA AND FREQUENCY OF BETA(S) AND BETA(C) GLOBIN IN IVORY-COAST
Authors: COULIBALY FH ELENGA OJP PREHU C ALLANGBA O KOFFI KG TOLO A TOURE AH SANOGO I KONATE S WACJMAN H SANGARE A GALACTEROS F
Citation: Fh. Coulibaly et al., MOLECULAR SCREENING FOR -3.7 KB DELETIONNAL ALPHA-THALASSEMIA AND FREQUENCY OF BETA(S) AND BETA(C) GLOBIN IN IVORY-COAST, Blood, 90(10), 1997, pp. 2843-2843
A MILDLY UNSTABLE HB VARIANT DUE TO DELETION OF 8 CODONS IN THE ALPHA-1 GENE - HB J-BISKRA
Authors: WAJCMAN H DAHMANE M PREHU C COSTES B PROME D AROUS N BARDAKDJIANMICHAU J RIOU J GODART C GALACTEROS F
Citation: H. Wajcman et al., A MILDLY UNSTABLE HB VARIANT DUE TO DELETION OF 8 CODONS IN THE ALPHA-1 GENE - HB J-BISKRA, Blood, 90(10), 1997, pp. 552-552
Risultati: 1-25 | 26-50 | 51-75 | 76-85