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Results: 1-25 | 26-45
Results: 1-25/45
CONE AND PLATE(LET) ANALYZER - MONITORING GLYCOPROTEIN IIB IIIA ANTAGONISTS AND VON-WILLEBRAND DISEASE REPLACEMENT THERAPY BY TESTING PLATELET DEPOSITION UNDER FLOW CONDITIONS/
Authors: VARON D LASHEVSKI I BRENNER B BEYAR R LANIR N TAMARIN I SAVION N
Citation: D. Varon et al., CONE AND PLATE(LET) ANALYZER - MONITORING GLYCOPROTEIN IIB IIIA ANTAGONISTS AND VON-WILLEBRAND DISEASE REPLACEMENT THERAPY BY TESTING PLATELET DEPOSITION UNDER FLOW CONDITIONS/, The American heart journal, 135(5), 1998, pp. 187-193
COEXISTENCE OF ACQUIRED PROTEIN-S AND PROTEIN-C DEFICIENCY AND THE ARG506GLN MUTATION IN FACTOR VA IN A CHILD WITH SEVERE THROMBOEMBOLIC DISEASE
Authors: SHAVIT I BRENNER B LANIR N KASSIS I LORBER A SHEHADEH N
Citation: I. Shavit et al., COEXISTENCE OF ACQUIRED PROTEIN-S AND PROTEIN-C DEFICIENCY AND THE ARG506GLN MUTATION IN FACTOR VA IN A CHILD WITH SEVERE THROMBOEMBOLIC DISEASE, Acta paediatrica, 87(3), 1998, pp. 349-350
REACTIVITY PATTERNS OF ANTIPHOSPHOLIPID ANTIBODIES AND ENDOTHELIAL-CELLS - EFFECT OF ANTIENDOTHELIAL ANTIBODIES ON CELL-MIGRATION
Authors: LANIR N ZILBERMAN M YRON I TENNENBAUM G SHECHTER Y BRENNER B
Citation: N. Lanir et al., REACTIVITY PATTERNS OF ANTIPHOSPHOLIPID ANTIBODIES AND ENDOTHELIAL-CELLS - EFFECT OF ANTIENDOTHELIAL ANTIBODIES ON CELL-MIGRATION, The Journal of laboratory and clinical medicine, 131(6), 1998, pp. 548-556
LONG-LASTING PROTECTIVE IMMUNITY TO EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS FOLLOWING VACCINATION WITH NAKED DNA ENCODING C-C CHEMOKINES
Authors: YOUSSEF S WILDBAUM G MAOR G LANIR N GOURLAVIE A GRABIE N KARIN N
Citation: S. Youssef et al., LONG-LASTING PROTECTIVE IMMUNITY TO EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS FOLLOWING VACCINATION WITH NAKED DNA ENCODING C-C CHEMOKINES, The Journal of immunology (1950), 161(8), 1998, pp. 3870-3879
THROMBOPHILIC POLYMORPHISMS IN WOMEN WITH RECURRENT FETAL LOSS
Authors: BRENNER B SARIG G WEINER Z YOUNIS J BLUMENFELD Z LANIR N
Citation: B. Brenner et al., THROMBOPHILIC POLYMORPHISMS IN WOMEN WITH RECURRENT FETAL LOSS, British Journal of Haematology, 102(1), 1998, pp. 250-251
BLEEDING PREDICTORS IN FACTOR-XI-DEFICIENT PATIENTS
Authors: BRENNER B LAOR A LUPO H ZIVELIN A LANIR N SELIGSOHN U
Citation: B. Brenner et al., BLEEDING PREDICTORS IN FACTOR-XI-DEFICIENT PATIENTS, Blood coagulation & fibrinolysis, 8(8), 1997, pp. 511-515
CLOT FORMATION ON CORONARY STENTS, EVALUATION BY IN-VITRO FLOW SYSTEM
Authors: LANIR N ZUK R BEYAR R BRENNER B
Citation: N. Lanir et al., CLOT FORMATION ON CORONARY STENTS, EVALUATION BY IN-VITRO FLOW SYSTEM, Thrombosis and haemostasis, 1997, pp. 433-433
A MISSENSE MUTATION IN GAMMA-GLUTAMYL CARBOXYLASE GENE CAUSES COMBINED DEFICIENCY OF VITAMIN-K-DEPENDENT BLOOD-COAGULATION FACTORS
Authors: SANCHEZVEGA B BRENNER B WU SM LANIR N MONTEJO JM STAFFORD DW SOLERA J
Citation: B. Sanchezvega et al., A MISSENSE MUTATION IN GAMMA-GLUTAMYL CARBOXYLASE GENE CAUSES COMBINED DEFICIENCY OF VITAMIN-K-DEPENDENT BLOOD-COAGULATION FACTORS, Thrombosis and haemostasis, 1997, pp. 1612-1612
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
AUTOSOMAL RECESSIVE NEPHROGENIC DIABETES-INSIPIDUS CAUSED BY AN AQUAPORIN-2 MUTATION
Authors: HOCHBERG Z VANLIEBURG A EVEN L BRENNER B LANIR N VANOOST BA KNOERS NVAM
Citation: Z. Hochberg et al., AUTOSOMAL RECESSIVE NEPHROGENIC DIABETES-INSIPIDUS CAUSED BY AN AQUAPORIN-2 MUTATION, The Journal of clinical endocrinology and metabolism, 82(2), 1997, pp. 686-689
ACTIVATED PROTEIN-C RESISTANCE CAN BE ASSOCIATED WITH RECURRENT FETALLOSS
Authors: BRENNER B MANDEL H LANIR N YOUNIS J ROTHBART H OHEL G BLUMENFELD Z
Citation: B. Brenner et al., ACTIVATED PROTEIN-C RESISTANCE CAN BE ASSOCIATED WITH RECURRENT FETALLOSS, British Journal of Haematology, 97(3), 1997, pp. 551-554
THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN JEWS STEM FROMDISTINCT FOUNDERS - ONE OF ANCIENT MIDDLE-EASTERN ORIGIN AND ANOTHER OF MORE RECENT EUROPEAN ORIGIN
Authors: PERETZ H MULAI A USHER S ZIVELIN A SEGAL A WEISMAN Z MITTELMAN M LUPO H LANIR N BRENNER B SHPILBERG O SELIGSOHN U
Citation: H. Peretz et al., THE 2 COMMON MUTATIONS CAUSING FACTOR-XI DEFICIENCY IN JEWS STEM FROMDISTINCT FOUNDERS - ONE OF ANCIENT MIDDLE-EASTERN ORIGIN AND ANOTHER OF MORE RECENT EUROPEAN ORIGIN, Blood, 90(7), 1997, pp. 2654-2659
BUDD-CHIARI-SYNDROME AND FACTOR-V-LEIDEN MUTATION
Authors: HOFFMAN R ASSY N BARUCH Y LANIR N BRENNER B
Citation: R. Hoffman et al., BUDD-CHIARI-SYNDROME AND FACTOR-V-LEIDEN MUTATION, Blood, 90(10), 1997, pp. 3229-3229
PROCOAGULANT AND ANTICOAGULANT MECHANISMS OF ACQUIRED APC RESISTANCE INDUCED BY ANTIPHOSPHOLIPID ANTIBODIES
Authors: LANIR N JACOBISHVILI J BRENNER B
Citation: N. Lanir et al., PROCOAGULANT AND ANTICOAGULANT MECHANISMS OF ACQUIRED APC RESISTANCE INDUCED BY ANTIPHOSPHOLIPID ANTIBODIES, Blood, 90(10), 1997, pp. 3242-3242
MONITORING GPIIB-IIIA ANTAGONISTS AND VWF REPLACEMENT THERAPY BY CONEAND PLATE(LET) ANALYZER (CPA)
Authors: VARON D DARDIK R SHENKMAN B TAMARIN I KENET G MARTINOWITZ U BEYAR R LASHEVSKY I LANIR N SAVION N
Citation: D. Varon et al., MONITORING GPIIB-IIIA ANTAGONISTS AND VWF REPLACEMENT THERAPY BY CONEAND PLATE(LET) ANALYZER (CPA), Blood, 90(10), 1997, pp. 3270-3270
A MISSENSE MUTATION IN GAMMA-GLUTAMYL CARBOXYLASE GENE CAUSES COMBINED DEFICIENCY OF VITAMIN-K-DEPENDENT BLOOD-COAGULATION FACTORS
Authors: BRENNER B SANCHEZVEGA B WU SM LANIR N MONTEJO JM STAFFORD DW SOLERA J
Citation: B. Brenner et al., A MISSENSE MUTATION IN GAMMA-GLUTAMYL CARBOXYLASE GENE CAUSES COMBINED DEFICIENCY OF VITAMIN-K-DEPENDENT BLOOD-COAGULATION FACTORS, Blood, 90(10), 1997, pp. 1284-1284
RETINAL ARTERIAL-OCCLUSION IN A CHILD WITH FACTOR-V-LEIDEN AND THERMOLABILE METHYLENE TETRAHYDROFOLATE REDUCTASE MUTATIONS
Authors: TALMON T SCHARF J MAYER E LANIR N MILLER B BRENNER B
Citation: T. Talmon et al., RETINAL ARTERIAL-OCCLUSION IN A CHILD WITH FACTOR-V-LEIDEN AND THERMOLABILE METHYLENE TETRAHYDROFOLATE REDUCTASE MUTATIONS, American journal of ophthalmology, 124(5), 1997, pp. 689-691
A STUDY OF COAGULATION AND ANTIENDOTHELIAL ANTIBODIES IN IDIOPATHIC LIVEDO-RETICULARIS
Authors: FACLIERU D BERGMAN R LANIR N FRIEDMANBIRNBAUM R BRENNER B
Citation: D. Faclieru et al., A STUDY OF COAGULATION AND ANTIENDOTHELIAL ANTIBODIES IN IDIOPATHIC LIVEDO-RETICULARIS, Acta dermato-venereologica, 77(3), 1997, pp. 181-183
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
IMMUNOREGULATORY EFFECTS OF INTERFERON-BETA AND INTERACTING CYTOKINESON HUMAN VASCULAR ENDOTHELIAL-CELLS IMPLICATIONS FOR MULTIPLE-SCLEROSIS AND OTHER AUTOIMMUNE-DISEASES
Authors: MILLER A LANIR N SHAPIRO S REVEL M HONIGMAN S KINARTY A LAHAT N
Citation: A. Miller et al., IMMUNOREGULATORY EFFECTS OF INTERFERON-BETA AND INTERACTING CYTOKINESON HUMAN VASCULAR ENDOTHELIAL-CELLS IMPLICATIONS FOR MULTIPLE-SCLEROSIS AND OTHER AUTOIMMUNE-DISEASES, Journal of neuroimmunology, 64(2), 1996, pp. 151-161
THROMBOEMBOLISM IN PARENTERAL-NUTRITION - ASSOCIATION WITH INTRAVENOUS FAT AND ANTIPHOSPHOLIPID ANTIBODIES
Authors: BERANT M SHAH V BENBARAK A LANIR N DOLLERY C MILLA PC
Citation: M. Berant et al., THROMBOEMBOLISM IN PARENTERAL-NUTRITION - ASSOCIATION WITH INTRAVENOUS FAT AND ANTIPHOSPHOLIPID ANTIBODIES, Pediatric research, 39(4), 1996, pp. 680-680
COEXISTENCE OF HEREDITARY HOMOCYSTINURIA AND FACTOR-V LEIDEN - EFFECTON THROMBOSIS
Authors: MANDEL H BRENNER B BERANT M ROSENBERG N LANIR N JAKOBS C FOWLER B SELIGSOHN U
Citation: H. Mandel et al., COEXISTENCE OF HEREDITARY HOMOCYSTINURIA AND FACTOR-V LEIDEN - EFFECTON THROMBOSIS, The New England journal of medicine, 334(12), 1996, pp. 763-768
COEXISTENCE OF FAMILIAL ANTIPHOSPHOLIPID SYNDROME AND FACTOR-V LEIDEN- IMPACT ON THROMBOTIC DIATHESIS
Authors: BRENNER B VULFSONS SL LANIR N NAHIR M
Citation: B. Brenner et al., COEXISTENCE OF FAMILIAL ANTIPHOSPHOLIPID SYNDROME AND FACTOR-V LEIDEN- IMPACT ON THROMBOTIC DIATHESIS, British Journal of Haematology, 94(1), 1996, pp. 166-167
HELLP-SYNDROME ASSOCIATED WITH FACTOR-V R506Q MUTATION
Authors: BRENNER B LANIR N THALER I
Citation: B. Brenner et al., HELLP-SYNDROME ASSOCIATED WITH FACTOR-V R506Q MUTATION, British Journal of Haematology, 92(4), 1996, pp. 999-1001
VENOUS THROMBOEMBOLISM ASSOCIATED WITH DOUBLE HETEROZYGOSITY FOR R506Q MUTATION OF FACTOR-V AND FOR T298M MUTATION OF PROTEIN-C IN A LARGE FAMILY OF A PREVIOUSLY DESCRIBED HOMOZYGOUS PROTEIN C-DEFICIENT NEWBORN WITH MASSIVE THROMBOSIS
Authors: BRENNER B ZIVELIN A LANIR N GREENGARD JS GRIFFIN JH SELIGSOHN U
Citation: B. Brenner et al., VENOUS THROMBOEMBOLISM ASSOCIATED WITH DOUBLE HETEROZYGOSITY FOR R506Q MUTATION OF FACTOR-V AND FOR T298M MUTATION OF PROTEIN-C IN A LARGE FAMILY OF A PREVIOUSLY DESCRIBED HOMOZYGOUS PROTEIN C-DEFICIENT NEWBORN WITH MASSIVE THROMBOSIS, Blood, 88(3), 1996, pp. 877-880
Risultati: 1-25 | 26-45