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Results: 1-23 |
Results: 23
LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I TO A LESS-THAN-1-CM INTERVAL ON CHROMOSOME 15Q15.1-15.3
Authors: TAMARY H SHALMON L SHALEV H HALIL A DOBRUSHIN D ASHKENAZI N ZOLDAN M RESNITZKY P KOROSTISHEVSKY M BONNETAMIR B ZAIZOV R
Citation: H. Tamary et al., LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I TO A LESS-THAN-1-CM INTERVAL ON CHROMOSOME 15Q15.1-15.3, American journal of human genetics, 62(5), 1998, pp. 1062-1069
VIREMIA, GENETIC-HETEROGENEITY, AND IMMUNITY TO HEPATITIS-G GB-C VIRUS IN MULTIPLY TRANSFUSED PATIENTS WITH THALASSEMIA
Authors: ZEMEL R DICKMAN R TAMARY H BUKH J ZAIZOV R TURKASPA R
Citation: R. Zemel et al., VIREMIA, GENETIC-HETEROGENEITY, AND IMMUNITY TO HEPATITIS-G GB-C VIRUS IN MULTIPLY TRANSFUSED PATIENTS WITH THALASSEMIA, Transfusion, 38(3), 1998, pp. 301-306
LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I TO A LESS-THAN 1CM ON CHROMOSOME 15Q15.1-5.3
Authors: TAMARY H SHALMON L SHALEV H DOBRUSHIN D ZOLDAN M RESNITZKY P SHAFT D KOROSTISHEVSKY M BONNETAMIR B ZAIZOV R
Citation: H. Tamary et al., LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I TO A LESS-THAN 1CM ON CHROMOSOME 15Q15.1-5.3, British Journal of Haematology, 102(1), 1998, pp. 300-300
MOLECULAR ANALYSIS OF A COMPOUND HETERO ZYGOTE FOR HYPOPROTHROMBINEMIA AND DYSPROTHROMBINEMIA (-G 7248 7249 AND ARG-340 TRP)/
Authors: TAMARY H SURREY S AUGUSTINE J SHALMON L SCHWARTZ E RAPPAPORT EF
Citation: H. Tamary et al., MOLECULAR ANALYSIS OF A COMPOUND HETERO ZYGOTE FOR HYPOPROTHROMBINEMIA AND DYSPROTHROMBINEMIA (-G 7248 7249 AND ARG-340 TRP)/, Blood coagulation & fibrinolysis, 8(6), 1997, pp. 337-343
ALPHA-THALASSEMIA CAUSED BY A 16 BP DELETION IN THE 3'-UNTRANSLATED REGION OF THE ALPHA-2-GLOBIN GENE INCLUDING THE FIRST NUCLEOTIDE OF THEPOLY-A SIGNAL SEQUENCE
Authors: TAMARY H KLINGER G SHALMON L ATTIAS D FORTINA P KOBAYASHI M SURREY S ZAIZOV R
Citation: H. Tamary et al., ALPHA-THALASSEMIA CAUSED BY A 16 BP DELETION IN THE 3'-UNTRANSLATED REGION OF THE ALPHA-2-GLOBIN GENE INCLUDING THE FIRST NUCLEOTIDE OF THEPOLY-A SIGNAL SEQUENCE, Hemoglobin, 21(2), 1997, pp. 121-130
2 NOVEL MUTATIONS CAUSING FACTOR-VII DEFICIENCY
Authors: TAMARY H FROMOVITCHAMIT Y SHALMON L ZIVELIN A PERETZ H LANIR N BRENNER B ZAIZOV R SELIGSOHN U
Citation: H. Tamary et al., 2 NOVEL MUTATIONS CAUSING FACTOR-VII DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 1686-1686
NEONATAL MANIFESTATIONS OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I
Authors: SHALEV H TAMARY H SHAFT D REZNITSKY P ZAIZOV R
Citation: H. Shalev et al., NEONATAL MANIFESTATIONS OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I, The Journal of pediatrics, 131(1), 1997, pp. 95-97
HODGKIN DISEASE IN CHILDREN - REDUCED TAILORED CHEMOTHERAPY FOR STAGEI-II DISEASE
Authors: YANIV I SAAB A COHEN IJ GOSHEN Y LOVEN D STARK B TAMARY H ZAIZOV R
Citation: I. Yaniv et al., HODGKIN DISEASE IN CHILDREN - REDUCED TAILORED CHEMOTHERAPY FOR STAGEI-II DISEASE, Journal of pediatric hematology/oncology, 18(1), 1996, pp. 76-80
RECOMBINANT-HUMAN-ERYTHROPOIETIN IN CHILDREN WITH CANCER
Authors: TAMARY H DANON YL
Citation: H. Tamary et Yl. Danon, RECOMBINANT-HUMAN-ERYTHROPOIETIN IN CHILDREN WITH CANCER, Pediatric hematology and oncology, 13(4), 1996, pp. 305-308
ALA244VAL IS A COMMON, PROBABLY ANCIENT MUTATION CAUSING FACTOR-VII DEFICIENCY IN MOROCCAN AND IRANIAN JEWS
Authors: TAMARY H FROMOVICH Y SHALMON L REICH Z DYM O LANIR N BRENNER B PAZ M LUDER AS BLAU O KOROSTISHEVSKY M ZAIZOV R SELIGSOHN U
Citation: H. Tamary et al., ALA244VAL IS A COMMON, PROBABLY ANCIENT MUTATION CAUSING FACTOR-VII DEFICIENCY IN MOROCCAN AND IRANIAN JEWS, Thrombosis and haemostasis, 76(3), 1996, pp. 283-291
LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I TO CHROMOSOME 15Q15.1-15.3
Authors: TAMARY H SHALMON L SHALEV H HALIL A SHAFT D ZOLDAN M RESNITZKY P KOROSTISHEVKY M ZAIZOV R
Citation: H. Tamary et al., LOCALIZATION OF THE GENE FOR CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I TO CHROMOSOME 15Q15.1-15.3, Blood, 88(10), 1996, pp. 563-563
CLINICAL-FEATURES AND STUDIES OF ERYTHROPOIESIS IN ISRAELI BEDOUINS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I
Authors: TAMARY H SHALEV H LURIA D SHAFT D ZOLDAN M SHALMON L GRUINSPAN A STARK B CHAISON M SHINAR E RESNITZKY P ZAIZOV R
Citation: H. Tamary et al., CLINICAL-FEATURES AND STUDIES OF ERYTHROPOIESIS IN ISRAELI BEDOUINS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I, Blood, 87(5), 1996, pp. 1763-1770
AN ALA-244 VAL MUTATION IN THE FACTOR-VII GENE IS COMMON IN JEWS OF DIFFERENT ETHNIC BACKGROUNDS
Authors: TAMARY H FROMOVITCH Y SHALMON L REICH Z DYM O LANIR N BRENNER B PAZ M LUDER AS BLAU O ZAIZOV R SELIGSOHN U
Citation: H. Tamary et al., AN ALA-244 VAL MUTATION IN THE FACTOR-VII GENE IS COMMON IN JEWS OF DIFFERENT ETHNIC BACKGROUNDS, Thrombosis and haemostasis, 73(6), 1995, pp. 1440-1440
ALPHA-THALASSEMIA INDUCED BY A NOVEL-16 PB DELETION IN THE ALPHA-2 GENE INCLUDING THE FIRST NUCLEOTIDE OF THE POLYA SIGNAL
Authors: TAMARY H KLINGER G SHALMON L ATTIAS D FORTINA P KOBAYASHI M SURREY S ZAIZOV R
Citation: H. Tamary et al., ALPHA-THALASSEMIA INDUCED BY A NOVEL-16 PB DELETION IN THE ALPHA-2 GENE INCLUDING THE FIRST NUCLEOTIDE OF THE POLYA SIGNAL, Blood, 86(10), 1995, pp. 2608-2608
CHRONIC CHILDHOOD IDIOPATHIC THROMBOCYTOPENIA PURPURA - LONG-TERM FOLLOW-UP
Authors: TAMARY H KAPLINSKY C LEVY I COHEN IJ YANIV I STARK B GOSHEN Y ZAIZOV R
Citation: H. Tamary et al., CHRONIC CHILDHOOD IDIOPATHIC THROMBOCYTOPENIA PURPURA - LONG-TERM FOLLOW-UP, Acta paediatrica, 83(9), 1994, pp. 931-934
HB TAYBE (ALPHA-38 OR ALPHA-39 THR DELETED) - AN ALPHA-GLOBIN DEFECT,SILENT IN THE HETEROZYGOUS STATE AND PRODUCING SEVERE HEMOLYTIC-ANEMIA IN THE HOMOZYGOUS
Authors: GALACTEROS F GIRODON E MRAD A MARTIN J GOOSSENS M JABER L COHEN IJ TAMARY H GOSHEN Y ZAIZOV R WAJCMAN H
Citation: F. Galacteros et al., HB TAYBE (ALPHA-38 OR ALPHA-39 THR DELETED) - AN ALPHA-GLOBIN DEFECT,SILENT IN THE HETEROZYGOUS STATE AND PRODUCING SEVERE HEMOLYTIC-ANEMIA IN THE HOMOZYGOUS, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 317(5), 1994, pp. 437-444
SYSTEMATIC USE OF AUTOMATED FLUORESCENCE-BASED SEQUENCE-ANALYSIS OF AMPLIFIED GENOMIC DNA FOR RAPID DETECTION OF POINT MUTATIONS
Authors: TAMARY H SURREY S KIRSCHMANN H SHALMON L ZAIZOV R SCHWARTZ E RAPPAPORT EF
Citation: H. Tamary et al., SYSTEMATIC USE OF AUTOMATED FLUORESCENCE-BASED SEQUENCE-ANALYSIS OF AMPLIFIED GENOMIC DNA FOR RAPID DETECTION OF POINT MUTATIONS, American journal of hematology, 46(2), 1994, pp. 127-133
THE PATTERN OF BONE-DISEASE IN TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS
Authors: KATZ K HOREV G GOSHEN J TAMARY H
Citation: K. Katz et al., THE PATTERN OF BONE-DISEASE IN TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS, Israel journal of medical sciences, 30(8), 1994, pp. 577-580
AMBULATORY TREATMENT WITH CEFTRIAXONE IN FEBRILE NEUTROPENIC CHILDREN
Authors: KAPLINSKY C DRUCKER M GOSHEN J TAMARY H COHEN IJ ZAIZOV R
Citation: C. Kaplinsky et al., AMBULATORY TREATMENT WITH CEFTRIAXONE IN FEBRILE NEUTROPENIC CHILDREN, Israel journal of medical sciences, 30(8), 1994, pp. 649-651
LONG-TERM INTRAVENOUS DEFEROXAMINE TREATMENT FOR NONCOMPLIANT TRANSFUSION-DEPENDENT BETA-THALASSEMIA PATIENTS
Authors: TAMARY H GOSHEN J CARMI D YANIV I KAPLINSKY C COHEN IJ ZAIZOV R
Citation: H. Tamary et al., LONG-TERM INTRAVENOUS DEFEROXAMINE TREATMENT FOR NONCOMPLIANT TRANSFUSION-DEPENDENT BETA-THALASSEMIA PATIENTS, Israel journal of medical sciences, 30(8), 1994, pp. 658-664
CLINICAL-FEATURES AND STUDIES OF ERYTHROPOIESIS IN BEDOUINS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I IN ISRAEL
Authors: TAMARY H SHALEV H LURIA D SHAFAT D ZOLDAN M SHALMON L GRUINSPAN A STARK B CHAISON M SHINAR E REZNITZKY P ZAIZOV R
Citation: H. Tamary et al., CLINICAL-FEATURES AND STUDIES OF ERYTHROPOIESIS IN BEDOUINS WITH CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-I IN ISRAEL, Blood, 84(10), 1994, pp. 10000503-10000503
HB SHELBY BETA-131(H9)GLN-!LYS! IN ASSOCIATION WITH HB-S BETA-6(A3)GLU-!VAL! - CHARACTERIZATION, STABILITY, AND EFFECTS ON HB S POLYMERIZATION
Authors: ADACHI K SURREY S TAMARY H KIM J ECK HS RAPPAPORT E OHENEFREMPONG K
Citation: K. Adachi et al., HB SHELBY BETA-131(H9)GLN-!LYS! IN ASSOCIATION WITH HB-S BETA-6(A3)GLU-!VAL! - CHARACTERIZATION, STABILITY, AND EFFECTS ON HB S POLYMERIZATION, Hemoglobin, 17(4), 1993, pp. 329-343
TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD - EVIDENCE FOR CELL-MEDIATED SUPPRESSION OF ERYTHROPOIESIS
Authors: TAMARY H KAPLINSKY C SHVARTZMAYER S UMIEL T PECHT M LEVIN S ZAIZOV R
Citation: H. Tamary et al., TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD - EVIDENCE FOR CELL-MEDIATED SUPPRESSION OF ERYTHROPOIESIS, The American journal of pediatric hematology/oncology, 15(4), 1993, pp. 386-391
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