Angiotensin; serum angiotensin-iconverting

Transcription

1 Subject Index Compiled G. Boehm, Basel (B) = Book Reviews Acetaldehyde influences glucose 1,6-biphosphate level of human erythrocytes in vitro and in vivo 241 Adenocarcinoma of the colon; acquired factor IX inhibitor in a patient with adenocarcinoma of the colon 49 Afibrinogenaemia; congenital afibrinogenaemia in a Saudi family: acasereportandfamilystudy 388 Alkaline phosphatase, v. Bone marrow, human (stroma) Alkaline phosphatase-positive leukaemic monocytes in a child with acute monocytic leukaemia 66 Anaemia, aplastic, acquired, prognosis 81 Anaemia, aplastic; immunological investigations in aplastic anaemia patients 178 Anaemia, dyserythropoietic, congenital, type II, associated with a new type of G6PD deficiency (G6PD Gabrovizza) 227 Anaemia, Fanconi s anaemia; increased activity of glutathione S- transferase and fast decay of reduced glutathione in Fanconi s anaemia erythrocytes 143 ; red blood cell hexokinase in Fanconi's anaemia 341 Anaemia, haemolytic, autoimmune, v. Haemoglobinuria Anaemia; sickle cell anaemia, erythrocyte density distribution 361 ; mild clinical course in two South African cases of sickle-cell anaemia 247 Angiotensin; serum angiotensin-iconverting enzyme and lysozyme levels in untreated and unsplenectomized patients with Hodgkin s disease 329 Antibodies, monoclonal, v. Killer cells; T-lymphoblastic leukaemia Anticoagulation; assessment of therapeutic control of anticoagulation 376 Aplasia of red cells, v. Congenital pure red cell aplasia Aplastic v. Anaemia, aplastic Arterial rupture, lumbar, secondary to iliopsoas haemorrhage in a haemophilic patient 128 Arthropathy, haemophilic, complicated by polyarticular septic arthritis 121 Asparaginase (L); pulmonary embolism and -asparaginase therapy 215 Assessment of therapeutic control of anticoagulation 376 Autoimmune haemolytic anaemia, associated with bone marrow sarcoidosis 204 ; v. Haemoglobinuria Autoradiography of white cells, labelled with techneticum 99m 13 Bernard-Soulier disease; diagnosis of heterozygous state for Bernard-Soulier disease 285 Beta-thromboglobulin in patients with high platelet count, clinical significance 32 Blood cells, white, v. White blood cells (B) Blood coagulation, v. Coagulation of blood Blood transfusion and immunology (Recent advances in haematology) 360(B) Blood transfusion; paediatrics and blood transfusion (Developments in hematology and immunology, vol. 2) 71 (B) Blood transfusions; acute graft-versus-host disease resulting from normal donor blood transfusion 270 Bone marrow, human; an enzymehistochemical approach to the study of human bone marrow stroma 71 Bone marrow sarcoidosis; autoimmune haemolytic anaemia associated with bone marrow sarcoidosis 204 Bone marrow smears, v. Haematopoietic committed progenitor cells, nuclear sizes Book reviews 71 (B), 216 (B), (B), 360(B), (B) C3 polymorphism in beta-thalassemia 45 Carcinoma, v. Adenocarcinoma Cardiovascular disease and thrombosis (Advances in experimental medicine and biology, vol. 164) 413(B) Castleman s disease, generalized, with urinary elimination of heavy chain fragments 400 CFU-GM (=colony-forming unitgranulocyte macrophage) colony-enhancing activity in sera of dogs under acute and chronic gamma-irradiation regimens 189 -; v. Granulomonocyte precursors, subpopulation

2 418 Subject Index Chédiak-Higashi disease, v. Leukaemia, myeloid, acute Children, v. Leukaemia, lymphoblastic, acute Chromosome 19; a new unusual translocation involving the short arms of chromosome 19 in Phlpositive chronic myeloid leukaemia 124 Coagulation of blood, v. Afribino- genaemia; Anticoagulation; Arthropathy; Bernard-Soulier disease, Beta-thromboglobulin; Cryoglobulin; Dysfibrinogenaemia; Factor VII; Factor VIII; Factor IX; Factor XIII; Haemophilia; Haemostasis; Heparintreated...; Platelet function (B); Thrombin; Thrombin formation (B); Thrombocytopenia; Thrombocytosis; Thrombosis (B); von WiUehrand's disease Cobalamin; serum cobalamin concentrations in sickle cell disease 299 Cobalamins (Methods in hematology) 287(B) Coeliac disease; hairy-cell leukaemia complicating chronic coeliac disease: report of a case and discussion of possible pathogenetic mechanisms 130 Colon, adenocarcinoma; acquired factor IX inhibitor in a patient with adenocarcinoma of the colon 49 Colony formation; CFU-GM colony-enhancing activity in sera of dogs under acute and chronic gamma-irradiation regimens 189 Colony-forming cells; in vitro colony-forming cells in embryonic mouse liver, spleen and peripheral blood 356 Complement; C3 polymorphism in beta-thalassemia 45 Congenital afibrinogenaemia in a Saudi family; a case report and family study 388 Congenital dyserythropoietic anaemia, type II, associated with a new type of G6PD deficiency (G6PD Gabrovizza) 227 Congenital pure red cell aplasia (Diamond-Blackfan syndrome); high-dose intravenous corticosteroid for a patient with Diamond-Blackfan syndrome refractory to classical prednisone treatment 207 Corticosteroids, v. Diamond-Blackfan syndrome Cryoglobulin, effects on fibrin clot formation and fibrinolysis 90 Cyprus, North Cyprus; prevalence of thalassaemia and G6PD deficiency in North Cyprus 69 Cytopenias; immune cytopenias 412(B) Cytotoxicity; phagocytosis-dependent neutrophil-mediated extracellular cytotoxicity against different target cells 371 v. Killer cells Density of erythrocytes; erythrocyte density distribution in sickle cell anaemia 361 Desferrioxamine; study of the mechanisms and sites of action of desferrioxamine in thalassaemia major 100 Diamond-Blackfan syndrome (treatment), v. Congenital pure red cell aplasia Dipcptidyl-amino-peptidase IV, (DAP IV), v. T cell chronic lymphocytic leukaemia Diphosphoglycerate; 2,3-diphosphoglycerate and P50 after exercise 410 DNA ( Desoxyribonucleic acid) structures, part I + II (Cold spring harbor symposia on quantitative biology, vol. 47) 412(B) Drug-induced thrombocytopenia, v. Indomethacin Dyserythropoietic anaemia, congenital, type II, associated with a new type of G6PD deficiency (G6PD Gabrovizza) 227 Dysfibrinogenemia, hereditary, characterized by slow fibrinopeptide release and competitive inhibition of thrombin 150 Dysfibrinogenemia, hereditary - the first 25 years 145 Electron microscopy (transmission and scanning), v. Congenital dyserythropoietic anaemia (trans.); Eosinophils (lacking peroxidase) (trans.); Hairy cell leukaemia (trans. a. scann.); Leukaemia, myeloid, acute (giant inclusions) (trans.); Lymphocytes, granular (trans.); Platelets (trans. a. scann.) Elliptocytosis, hereditary, with a spectrin molecular defect in a white patient 235 Embryonic blood, v. Mouse (colony-forming cells) Enzymatic analysis, methods (3rd ed.) (vol. 1: Fundamentals) 288 (B) Enzyme-histochemical approach to the study of the human bone marrow stroma 71 Eosinophils, human, genetically lacking peroxidase, ultrastructure 334 Erythrocyte density distribution in sickle cell anaemia 361 Erythrocyte ferritin in thalassaemia syndromes 251 Erythrocyte membrane sialic acid in new-born infants 198 Erythrocyte volume; haemoglobin phenotype and mean erythrocyte volume in Sicilian people 214 Erythrocytes; acetaldehyde influences glucose 1,6-biphosphate level of human erythrocytes in vitro and in vivo 241 -; congenital pure erythrocyte aplasia (Diamond-Blackfan syndrome); high-dose intravenous corticosteroid for a patient with

3 Subject Index 419 Diamond-Blackfan syndrome refractory to classical prednisone treatment 207 hereditary elliptocytosis with a spectrin molecular defect in a white patient 235 red blood cell hexokinase in Fanconi s anaemia 341 v. congenital dyserythropoietic anaemia Erythropoietin levels in heterozygous beta-thalassaemia 211 Exercise; 2,3-diphosphoglycerate and Pso after exercise 410 Factor VII (-proconvertin/convertin) congenital deficiency and thromboembolism 60 Factor VIII («antihaemophilic globulin A) deficiency; association of the haemophilia A carrier state and haemorrhagicthrombocytopathy with dilatation of the platelet membrane complex 381 -;v. von Willebrand'sdisease Factor IX (-antihaemophilic globulin B); acquired factor IX inhibitor in a patient with adenocarcinoma of the colon 49 Factor XIII (=fibrin-stabilizing factor), acquired inhibitor, with a qualitative abnormality of fibrin cross-linking 304 Families, v. Afibrinogenaemia; Dysfibrinogenaemia; Factor VII (congenital deficiency); Haemophilia A carrier state Fanconi s anaemia; increased activity of glutathione S-transferase and fast decay of reduced glutathione in Fanconi s anaemia erythrocytes 143 Fanconi s anaemia; red blood cell hexokinase in Fanconi's anaemia 341 Ferments, v. Alkaline phosphatase; Alkaline phosphatase-positive leukaemic monocytes; Asparaginase; Dipeptidyl-amino-peptidase; Enzymatic analysis (B); Enzyme-histochemical...; Glucose-6-phosphate dehydrogenase; Glutathione S-transferase; Hexokinase; Lysozyme Ferritin; changes in superoxide anion production in neutrophils from multitransfused i-thalassaemia patients: correlation with ferritin levels and liver damage 289 -; erythrocyte ferritin in thalassaemia syndrome 251 -; serum ferritin in evaluation of iron status in children 111 Ferritin-secreting cells, circulating, enumeration by a reverse hemolytic plaque assay 39 Ferrokinetics, v. Desferrioxamine Fetal erythrocyte, v. Sialic acid Fibrin; acquired inhibitor of factor XIII with a qualitative abnormality of fibrin cross-linking 304 Fibrin clot formation and fibrinolysis, effects of cryoglobulin 90 Fibrinogen, v. Afibrinogenaemia; Dysfibrinogenaemia (fibrinogen Charlottesville) Fibrinolysis; effect of cryoglobulin on fibrin clot formation and fibrinolysis 90 Fibrinopeptide release, slow, v. Dysfibrinogenemia Fibronectin; plasma beta-2-microglobulin and fibronectin levels in beta-thalassaemia 257 Gamma irradiation, v. Irradiation, gamma irradiation Glucose 1,6-biphosphate; acetaldehyde influences glucose 1,6-biphosphate level of human erythrocytes in vitro and in vivo 241 Glucose-6-phosphate dehydrogenase (G6PD) deficiency; congenital dyserythropoietic anaemia type II, associated with a new type of G6PD deficiency (G6PD Gabrovizza) 227 ; prevalence of thalassaemia and G6PD deficiency in North Cyprus69 Glutathione S-transferase, increased activity and fast decay of reduced glutathione in Fanconi s anaemia erythrocytes 143 Graft-versus-host disease, acute, resulting from normal donor blood transfusions 270 Granular lymphocytes (abnormal expansion), v. Lymphocytes, granular Granulomonocyte precursors; retinoic acid enhances the growth of only one subpopulation of granulomonocyte precursors 97 Haemangioma of the liver, v. Hairy cell leukaemia Haematopoiesis, v. Colony-forming cells Haematopoietic committed progenitor cells, nuclear sizes, measurement, compared to leukemic blasts from human bone marrow smears 8 Haemoglobin phenotype and mean erythrocyte volume in Sicilian people 214 Haemoglobinuria, paroxysmal, nocturnal (A clinicopathological study of 26 cases) 217 Haemolytic anaemia, autoimmune, associated with bone marrow sarcoidosis 204 Haemophilia; lumbar arterial rupture secondary to iliopsoas haemorrhage in a haemophilic patient 128 Haemophilia A; association of the haemophilia A carrier state and haemorrhagic thrombocytopathy with dilatation of the platelet membrane complex 381 Haemophilic arthropathy complicated by polyarticular septic arthritis 121 Haemostasis; synthetic substrates in haemostatic testing: current status and future trends (Minisymposium: Stritch School of

4 420 Subject Index Medicine, Loyola University, and thymic cysts 282 Medical Center) Maywood 111. USA; (July 27, 1984) 360 Hair, v. Zinc Hairy cell leukaemia; report of an unusual case with hepatomegaly ; serum angiotensin-i-converting enzyme and lysozyme levels in unsplenectomized patients with Hodgking s disease 329 ; v. Graft-versus-host disease due to a large vascular tumor of Hypergammaglobulinaemic purpura; the liver, mediastinal mass and therapy of Waldenstrom s pleural effusion containing hairy benign hypergammaglobulincells 393 Hairy-cell leukaemia complicating coeliac disease; report of a case aemia by regular plasmapheresis 345 Hypersplenism, v. Fibronectin and discussion of possible pathogenetic Hypogammaglobulinaemia, v. mechanisms 130 Heavy chain disease; sequential development Anaemia, aplastic (immunological investigations) of Waldenstrom's macroglobulinaemia and gamma-1-heavy chain disease in a single patient (Clinical, immunochemical, Idiopathic thrombocytopenic purpura, v. Thrombocytopenia IgG, v. Castleman's disease; Plas immunofluorescent ma cell leukaemia and protein studies) 53 Heavy chain fragments, urinary elimination, in generalized Castleman s disease 400 Hemalog D ; evaluation of the use of the Hemalog D in acute lymphoblastic leukaemia and disseminated non-hodgkin's lymphoma in children 18 IgG, polyclonal, v. Hypergammaglobulinaemic purpura Iliopsoas haemorrhage, v. Haemophilia Immune cytopenias 412(B) Immunological investigations in aplastic anaemia patients 178 Immunology and blood transfusion (Recent advances in haematology) Heparin-treated patients, spontaneous 360(B) platelet aggregation 63 Hepatomegaly, v. Vascular tumor of the liver Inclusions, giant, v. Leukaemia, myeloid, acute Indomethacin; acute thrombocytopenia Hereditary dysfibrinogenemia following ingestion of characterized by slow fibrinopeptide release and competitive inhibition of thrombin 150 Hereditary dysfibrinogenemia - the first 25 years 145 Hereditary elliptocytosis with a spectrin molecular defect in a white patient 235 Histochemical method; an enzymeindomethacin 350 Iron status in children, evaluation, with serum ferritin 111 Iron, v. Desferrioxamine Irradiation, gamma irradiation; CFU-GM colony-enhancing activity in sera of dogs under acute and chronic gamma-irradiation regimens 189 histochemical approach to the study of the human bone marrow stroma 71 Killer cells; natural killer cell activity and T subpopulations in thal- Hodgkin s disease; an unusually severe subacute motor neuronopa- assaemia major 263 thy in Hodgkin's disease 136 ; mediastinal Hodgkin's disease Lymphocytes, granular Leukaemia, hairy cell leukaemia; complicating chronic coeliac disease: report of a case and discussion of possible pathogenetic mechanisms 130 ; report of an unusual case with hepatomegaly due to a large vascular tumor of the liver, mediastinal mass and pleural effusion containing hairy cells 393 Leukaemia, lymphoblastic, acute; evaluation of the use of Hemalog D in acute lymphoblastic leukaemia and disseminated non- Hodgkin'.s lymphoma in children 18 ; T-acute lymphoblastic leukaemia related to intermediate cortical/medullary thymocytes displaying functional and surface characteristics of suppressor T cells 1 Leukaemia, lymphocytic, chronic; heterogeneous expression of di- peptidyl-amino-peptidase IV (DAP IV) in T cell chronic leukaemia 277 ; levamisole in chronic lymphocytic leukaemia (B-cell): a prospective study of 15 patients 316 Leukaemia, monocytic, acute; alkaline phosphatase-positive leukaemic monocytes in a child with acute monocytic leukaemia 66 ; v. Monocytic sarcoma (sclera) Leukaemia, myeloblastic, acute, presenting with superior vena cava syndrome due to mediastinal mass 174 Leukaemia, myeloid, acute, with giant inclusions in the myeloblasts: cytochemical and ultrastructural study 165 Leukaemia, myeloid, chronic; a new unusual translocation involving the short arms of chromosome 19 in Phi-positive chronic myeloid leukaemia 124

5 Subject Index 421 Leukaemia; plasma cell leukaemia relapsing in the dermis 359 Leukaemic blasts, v. Haematopoietic committed progenitor cells, nuclear sizes Levamisole in chronic lymphocytic leukaemia: a prospective study of 15 patients 316 Lipoproteins; plasma lipids and lipoproteins pattern in beta-thalassaemia major 106 Liver disease, v. Superoxide anion productions (neutrophils) Liver (embryonic), v. Mouse (colony-forming cells) Lumbar arterial rupture secondary to illiopsoas haemorrhage in a haemophilic patient 128 Lymph node enlargement, generalized, v. Castleman'sdisease Lymphoblasts, v. Hemalog D Lymphocyte populations and T cell subpopulations in blood of patients with non-hodgkin lymphomas 322 Lymphocyte transformation, v. Anaemia, aplastic (immunological investigations) Lymphocytes, granular; unusual phenotype (Leu7*, OKT4*, OKM1") expressed by cells from a patient with an abnormal expansion of granular lymphocytes 310 Lymphocytes, granular, v. Killer cells Lymphocytes, T-lymphocyies, v. T-lymphoblastic leukaemia Lymphocytosis, v. Lymphocytes, granular (abnormal expansion) Lymphomas, non-hodgkin, lymphocyte populations and T cell subpopulations in blood of patients with non-hodgkin lymphomas 322 Lysozyme; serum angiotensin-iconverting enzyme and lysozyme levels in untreated and unsplenectomized patients with Hodgkin s disease 329 Macroglobulinaemia, v. Waldenstrom s macroglobulinaemia Mediastinal Hodgkin's disease and thymic cysts 282 Mediastinal mass, large, paratrachéal. v. Hairy cell leukaemia Mediastinal mass, v. Superior vena cava syndrome Membrane of erythrocytes, v. Spectrin Methods of enzymatic analysis (3rd ed.) (vol. 1: Fundamentals) 288(B) Methods in haematology, v. Cobalamins (B); Platelet function (B); Thrombin formation (B) Microcirculation reviews I: white blood cells 413(B) Microglobulin, /?2-microgIobulin; plasmabeta-2-microglobulin and fibronectin in beta-thalassaemia 257 Monoclonal antibodies, v. Killer cells; Lymphocytes, granular (abnormal expansion); Non- Hodgkin s lymphomas; T-cell chronic lymphocytic...; T-lymphoblastic leukaemia Monocytes; alkaline phosphatasepositive leukemic monocytes in a child with acute monocytic leukaemia 66 Monocytic sarcoma of the sclera 407 Mononuclear cells in the peripheral blood, v. Ferritin-secreting cells Motor neuronopathy; an unusually severe subacute motor neuronopathy in Hodgkin s disease 135 Mouse, embryonic liver and spleen; in vitro colony-forming cells in embryonic mouse liver, spleen and peripheral blood 356 Multiple myeloma, v. Myeloma, multiple Myelom, multiples (Diagnose, Klinik und Therapie) 216(B) Myeloma, multiple; clinical observations showing the role of some factors in etiology of multiple myeloma (A study in 7 patients) 116 ; Pancoast s syndrome in multiple myeloma 353 Naphthyl-acetate-esterase (a- Naphtyl...), v. Bone marrow, human (stroma) Natural killer cells, v. Killer cells Neuronopathy; an unusually severe subacute motor neuronopathy in Hodgkin's disease 135 Neutrophils; phagocytosis-dependent neutrophil-mediated extracellular cytotoxicity against different target cells 371 Neutrophils, superoxide anion production; changes in superoxide anion production in neutrophils from multitransfused ß- thalassaemia patients; correlation with ferritin levels and liver damage 289 Nocturnal paroxysmal haemoglobinuria, v. Haemoglobinuria Non-Hodgkin s lymphoma; evaluation of the use of Hemalog D in acute lymphoblastic leukaemia and disseminated non- Hodgkin s lymphoma in children 18 ; lymphocyte populations and T cell subpopulations in blood of patients with non-hodgkin lymphomas 322 Nuclear sizes of committed haematopoietic progenitor cells, measurements, compared to leukemic blasts from human bone marrow smears 8 P50 (=partial pressure of oxygen at 50% oxygenation of haemoglobin), v. Diphosphoglycerate Paediatrics and blood transfusion (Developments in hematology and immunology, vol. 2) 71 (B) Pancoast s syndrome in multiple myeloma 353

6 422 Subject Index Paroxysmal nocturnal haemoglobinuria (A clinicopathological study of 26 cases) 217 Peroxidase; ultrastructure of human oesinophils genetically lacking peroxidase 334 Phagocytosis v. Superoxide anion production Phagocytosis-dependent neutrophil-mediated extracellular cytotoxicity against different target cells 371 Phenotype (Leu 7 \ O K T 4\ OKM 1+), unusual, expressed by cells from a patient with an abnormal expansion of granular lymphocytes 310 Philadelphia chromosome, v. Leukaemia, myeloid, chronic Phosphatase, v. Alkaline phosphatase-positive leukaemic monocytes; Bone marrow, human (stroma) Plaque-forming cells, v. Reverse hemolytic plaque assay Plasma beta-2-microglobulin and fibronectin levels in beta-thalassaemia 257 Plasma cell leukaemia relapsing in the dermis 359 Plasma lipids and lipoproteins pattern in beta-thalassaemia major 106 Plasmacytoma, v. Pancoast's syndrome Plasmapheresis; therapy of Waldenstrom s benign hypergammaglobulinaemia by regular plasmapheresis 345 Platelet aggregation; atypical von Willebrand s disease with hyperreactivity of platelet aggregation 158 ; spontaneous, in heparin-treated patients 63 Platelet count, high; clinical significance of beta-thromboglobulin in patients with high platelet count 32 Platelet function, measurements (Methods in haematology, vol.8) 287(B) Platelet size in thrombocytosis 144 Platelet volume indices in the etiological diagnosis of thrombocytopenia, a discriminant study 25 Platelets; association of the haemophilia A carrier state and haemorrhagic thrombocytopathv with dilatation of the platelet membrane complex 381 Platelets, large (aggregation) v. Bernard-Soulier disease Pleural effusion, v. Hairy ceil leukaemia (unusual case) Polyarticular arthritis, v. Arthropathy Prednisone, v. Factor IX (inhibitor) Progenitor cells, committed, v. Haemopoietic committed progenitor cells, nuclear sizes Proteins, circulating; Quantification of circulating proteins (Theory and applications based on a- nalysis of protein levels) 216 (B) Pulmonary embolism and -asparaginase therapy 215 Purpura, hypergammaglobulinaemic, Waldenstrom's, v. Hypergammaglobulinaemic purpura Purpura, thrombocytopenic, idiopathic, v. Thrombocytopenia Quantification of circulating proteins (Theory and applications based on analysis of protein levels) 216(B) Red blood cell(s), v. Erythrocyte(s) Retinoic acid enhances the growth of only one subpopulation of granulomonocyte precursors 97 Reverse hemolytic plaque assay, v. Ferritin-secreting cells, circulating Ristocetin, v. von Willebrand s disease Sarcoidosis of bone marrow; autoimmune haemolytic anaemia associated with bone marrow sarcoidosis 204 Sarcoma, monocytic, of the sclera 407 Saudi family; congenital afibrinogenaemia in a Saudi family; a case report and family study 388 Sclera, monocytic sarcoma 407 Septic arthritis, v. Arthropathy Sera of dogs under acute and chronic gamma-irradiation regimens, CFU-GM colony-enhancing activity 189 Serotonin, v. Platelet count, high Serum angiotensin-i-converting enzyme and lysozyme levels in untreated and unsplenectomized patients with Hodgkin's disease 329 Serum cobalamin concentration in sickle cell disease (HbSS) 299 Serum ferritin in evaluation of iron status in children 111 v. Ferritin Serum, v. Zinc Sialic acid; erythrocyte membrane sialic acid in new-born infants 198 Sicilian people; haemoglobin phenotype and mean erythrocyte volume in Sicilian people 214 Sickle cell anaemia, erythrocyte density distribution 361 ; mild clinical course in two South African cases of sickle-cell anaemia 247 Sickle cell disease, serum cobalamin concentration 299 South Africa, v. Sickle-cell anaemia Spectrin; hereditary elliptocytosis with a spectrin molecular defect in a white patient 235 Spleen (Clinics in haematology, vol. 12, No. 2) 360(B) Spleen in health and disease 287 (B) Spleen (embryonic), v. Mouse (colony forming cells) Splenectomy, v. Lysozyme Stroma of the human bone marrow, v. Bone marrow, human

7 Subject Index 423 Superior vena cava syndrome; acute myeloblastic leukaemia presenting with superior vena cava syndrome due to mediastinal mass 174 Superoxide anion production in neurtophils from multitransfused /3-thalassaemia patients, changes: correlation with ferritin levels and liver damage 289 Suppressor T cells, v. T-lymphoblastic leukaemia WmTc, v. Technetium 99m T-cell chronic lymphocytic leukaemia; heterogeneous expression of dipeptidyl-amino-peptidase IV (DAP IV) in T-cell chronic lymphocytic leukaemia 277 T cell subpopulations; lymphocyte populations and T cell subpopulations in blood of patients with non-hodgkin lymphomas 322 ; natural killer cell activity and T subpopulations in thalassaemia major 263 T cell subsets, v. Anaemia, aplastic (immunological investigations) Technetium 99m autoradiography of labelled white cells 13 Thalassaemia; erythrocyte ferritin in thalassaemia syndromes 251 Thalassaemia; prevalence of thalassaemia and G6PD deficiency in North Cyprus 69 Thalassaemia: recent advances in detection and treatment (Birth defects; original article series) 71 (B) Thalassaemia (alpha), v. Sickle cell anaemia Thalassaemia (beta); C3 polymorphism in beta-thalassaemia 45 ; changes in superoxide anion production in neutrophils from multitransfused /J-thalassaemia patients: correlation with ferritin levels and liver damage 289 ; erythropoietin levels in heterozygous beta-thalassaemia 211 ; plasma beta-2-microglobulin and fibronectin levels in betathalassaemia 257 ; zinc levels of serum, hair and urine in homozygous beta-thalassaemic subjects under hypertransfusional treatments 139 Thalassaemia major; study of the mechanisms and sites of action of desferrioxamine in thalassaemia major 100 Thalassaemia major (beta); natural killer cell activity and T subpopulations in thalassaemia major 263 ; plasma lipids and lipoproteins pattern in beta-thalassaemia major 106 Thalassaemia trait, v. Thalassaemia (beta) Therapeutic control of anticoagulation, assessement 376 Therapy of Waldenstrom's benign hypergammaglobulinaemia by regular plasmapheresis 345 Therapy, v. Diamond-Blackfan syndrome; Levamisole; Pulmonary embolism Thrombin; hereditary dysfibrinogenemia characterized by slow fibrinopeptide release and competitive inhibition of thrombin 150 Thrombin formation, disorders (Methods in hematology, vol. 5) 288 (B) Thrombocytopathy, haemorrhagic; association of the haemophilia A carrier state and haemorrhagic thrombocytopathy with dilatation of the platelet membrane complex 381 Thrombocytopenia; discriminant study of platelet volume indices in the etiological diagnosis of thrombocytopenia 25 Thrombocytopenia, acute, following ingestion of indomethacin 350 Thrombocytopenic purpura, idiopathic, v. Thrombocytopenia Thrombocytosis, platelet size 144 -; v. Platelet count, high Thromboembolism in congenital factor VII deficiency 60 Thromboglobulin, v. Beta-thromboglobulin Thrombosis and cardiovascular diseases (Advances in experimental medicine and biology, vol. 164) 413(B) Thymic cysts; mediastinal Hodgkin's disease and thymic cysts 282 Thymocytes, differentiation, v. T-lymphoblastic leukaemia T-lymphoblastic leukaemia, acute, related to intermediate cortical/ medullary thymocytes displaying functional and surface characteristics of suppressor cells 1 Tracks, visible, v. Technetium 99m Transfusion, v. Blood transfusion (B); Blood transfusions Transfusion (hypertransfusional treatment), v. Thalassaemia (beta) (zinc levels) Translocation, unusual, v. Chromosome 19 T subpopulations in thalassaemia major and natural killer cell activity 263 Ultrastructure of human eosinophils genetically lacking peroxidase 334 Ultrastructure, v. Congenital dyserythropoietic anaemia; Hairy cell leukaemia; Leukaemia, myeloid, acute (giant inclusions); Platelets Urine, v. Zinc Vascular tumor of the liver; hairy cell leukaemia; report of an unusual case with hepatomegaly due to a large vascular tumor of the liver, mediastinal mass and pleural effusion containing hairy cells 393

8 424 Subject Index Vena cava, superior; acute myeloblastic leukaemia presenting with superior vena cava syndrome due to mediastinal mass 174 Vitamin B,,, v. Cobalamine, Cobalamins(B) von Willebrand's disease, atypical, with hyperreactivity of platelet aggregation 158 Waldenstrom's benign hypergammaglobulinaemia, therapy by regular plasmapheresis 345 Waldenstrom s macroglobulinaemia; sequential development of Waldenstrom's macroglobulinaemia and gamma-1-heavy chain disease in a single patient (Clinical, immunochemical, immunofluorescent and protein studies) 53 Warfarin, v. Anticoagulation White blood cells (Microcirculation reviews I) 414(B) White blood cells; technetium 99m autoradiography of labelled white blood cells 13 Willebrand, v. von Willebrand Zinc levels of serum, hair and urine in homozygous beta-thalassaemic subjects under hypertransfusional treatment 139 Zymosan particles, opsonized, v. Cytotoxicity