Abe, M.

Defibrination Syndrome Developed after Replacement Therapy with PPSB in a Case of Hemophilia B.

Abe, T.

Defibrination Syndrome Developed after Replacement Therapy with PPSB in a Case of Hemophilia B.

Abildgaard, C.

Multiple Molecular forms of Factor VIII Antigen in Normal Individuals and von Willebrand’s Disease Patients

Ackerman, L.L.

Personality Characteristics of Hemophiliac Children

Clinical Severity, Personality Characteristics and Maternal Attitudes in Hemophiliac Children

Effects of Psychiatric Intervention on Concentrate Usage

Personality Characteristics of Adult Hemophiliacs

Ageron, M.H.

Femoral Fractures in Severe Hemophilia

Aledort, L.

Component Therapy Fractionation and the Economics of a Regionalized Blood Delivery System

Allain, J.P.

History of Care for the Hemophiliac in France: Movement from Special Hospital to Home Care

Psychological Aspects of Training for home Treatment in Hemophilia

Femoral Fractures in Severe Hemophilia

Dose Requirement for Substitution Therapy in Hemophilia A.

Femoro-Patellar Syndrome in Hemophilic Knee

Amitrani, Paul

Legal Ways to Contest job Discrimination Among Hemophiliacs

Anderle, K.

The Use of Fibroseal in Hemophilic Cysts - A Case Report

The Clinical Application of Feiba Immuno in Factor VIII Inhibitor Patients

Anderson, L.C.

Home Treatment for Children with Hemophilia

Arblaster, P.G.

A Comparison of Current Prophylactic Therapy in Canada and the United Kingdom

Aronstam, A.

A Comparison of Current Prophylactic Therapy in Canada and the United Kingdom

Austen, D. E. G.

Large Scale Purification and Characterisation of Porcine Factor VIII for Clinical Use

Azevedo, C.B.

A Case of Henoch-Schoenlein Purpura in Hemophilia

Baicchi, U.

Four Years’ Follow-Up Study of Liver Function of Haemophiliacs

Electroimmunoassay of Factor IX in the Detection of Haemophilia B Carriers

Ballard, J.O.

Comparison of Factor VIII Levels After Adrenalin IN Hemophilia a and von Willebrand’s Disease (VWD)

Baré, L.F.

A Case of Henoch-Schoenlein Purpura in Hemophilia

Barr, J.D.

The Need to Filter Cryoprecipitate. A Microscopic Assessment of Filter Deposition

The Hemophiliac and Knowledge of Their Condition

Baudo, F.

The Use of Fibroseal in Hemophilic Cysts - A Case Report

Beck, E.A.

Degradation of Factor VIII-Related Protein in Factor VIII Concentrates

Chemical Cross-Linking of Factor VIII Subunits

Beeser, H.

Further Experience on the Effect of High Pre-Donation Factor VIII Levels in Blood Donors on the Factor VIII Content of Small-Pool Fractions

Belbeck, L.

Chemical Synovectomy in Induced Haemophiliac Synovitis

Bellamy, A.

Social Support Systems in the Treatment Programme of Haemophilia in new South Wales, Australia

Bennetts, Geni A.

Elective Synovectomy in Hemophilia

Benson, R.E.

Autosomal Factor VIII Deficiency in Rabbits: Size Variations of Rabbit Factor VIII.

Bernabei, P.

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Berry, E.W.

Local use of Epsilon-Aminocaproic Acid in Dental Therapy

Berry, P.R.

Local use of Epsilon-Aminocaproic Acid in Dental Therapy

Bertina, R.M.

Carrier Detection in Hemophilia B.

Bick, R.L.

The Large Scale Preparation of Clottable Fibrinogen-Free, High Purity, High Potency Factor VIII Concentrate

Bidwell, E.

Session: Hemophilia Therapy: A Challenge to the World Blood Resources” Topic: “How can the Problem be Solved? Is Blood a World Resource?”

Birardi, F.

Nitro Bleu Tetrazolium Reduction test in Hemophilia

Blewitt, Rita E.

Large Scale Purification and Characterisation of Porcine Factor VIII for Clinical Use

Böhler, Wien N.

The Use of Fibroseal in Hemophilic Cysts - A Case Report

Boncompagni, L.

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Bonomo, L.

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Boone, D.C.

Plasma Concentrate Consumption - A Five Year Study

Non-Surgical Methods for Correction of Knee Flexion Contracture.

Booyse, F.

The Interaction of the Platelet and von Willebrand Factor

Bosch, N.B.

Nerve Lesions in Haemophilia

Boscho, N.B.

Radioactive Synoviorthesis in Haemophiliac Haemarthrosis

Bosser, C.

“Santal” a Hemophiliac Data Bank in the Network Cyclades

Böttcher, D.

Hemophilia a and Variant of von Willebrand’s Disease in one Family

Immunologic Studies in Patients with Von Willebrand’s Disease

Bottini, F.R.

HB_S and “e” Antigen-Antibody Systems in a Population of Hemophiliacs

Boudreaux, H.B.

Oral Prophylactic Therapy in Hemophilia A and B (Factor VIII and IX Deficiencies)

Boutaugh, M.

Michigan’s Summer camp for Hemophiliacs

Low Dose Factor Replacement in the Hemophiliac

Bowie, E. J. W.

The Interaction of the Platelet and von Willebrand Factor

Brackmann, H.H.

Biomechanical Alterations Caused by Musculo’s Keletal Bleedings.

Home Care in Germany: Philosophy of Treatment, Results of Intensive Care

Brackmann, H.-H.

The Successful Treatment of Aquired Inhibitors Against Factor VIII.

Briët, E.

Carrier Detection in Hemophilia B.

Britten, Anthony F. H.

Factor VIII Concentrates - Forces of Supply and Demand

Caffinière, J.Y. De La

Femoro-Patellar Syndrome in Hemophilic Knee

Caldwell, A.

Personality Characteristics of Adult Hemophiliacs

Capitanio, A.

Significance of Abnormal Liver Function Tests in Hemophiliacs: A Follow-Up Study

Casillas, G.

Bovine Factor VIII. Antigens and Biological Activities

Cavalcanti, Wellington

Case Histories

Cea, J.

The Role of the Dental Hygienist in a Community Hospital Hemophilia Program

Cerullo, L.

Head Trauma in Hemophilia: Value of Computer Tomography of The Brain in Localizing Multiple Hematomas

Chantarangkul, V.

An Artificial ‘Haemophilic’ Plasma for One-Stage Factor VIII Assay

Charney, D.

Effects of Psychiatric Intervention on Concentrate Usage

Charney, D.S.

Personality Characteristics of Hemophiliac Children

Clinical Severity, Personality Characteristics and Maternal Attitudes in Hemophiliac Children

Personality Characteristics of Adult Hemophiliacs

Chauvin, W.J.

The Need to Filter Cryoprecipitate. A Microscopic Assessment of Filter Deposition

Chavin, S.I.

Large Scale Purification and Characterisation of Porcine Factor VIII for Clinical Use

Cheng, T.

Convenient Microtiter assay for von Willebrand’s Factor

Child, D.

The All-American Blood Buddy: Donor Motivation for Hemophilia and Other Chronic Disorders

Child, Dorothy

The Role of the Consumer-Patient in the Growth of a Comprehensive Hemophilia Care Unit

Chin, J.

A Computer Analysis of Patient Activity and Blood Product Usage in Community Hospital Hemophilia Program

Chung, K.S.

Mutant forms of Factor IX

Ciavarella, N.

Feasibility of Antifibrinolytic Treatment in Hemophilia: Preliminary Study

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Psychological Studies in Hemophiliacs in a Summer Camp

Cole, F.M.

Chemical Synovectomy in Induced Haemophiliac Synovitis

Collen, D.

A Multicenter Evaluation of an Activated Partial Thromboplastin Time Test, Cepho-Test

Coster, A.B.

Local use of Epsilon-Aminocaproic Acid in Dental Therapy

Coviello, M.

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Csörgö, M.

Diagnostic and Therapeutic Problems in a Patient with Factor VIII Inhibitor

Darby, S.

An Artificial ‘Haemophilic’ Plasma for One-Stage Factor VIII Assay

Darracott, J.

Chemical Synovectomy in Induced Haemophiliac Synovitis

Davey, Fredrick

The Aspirin Bleeding Time - A Screening Test for Evaluation of von Willebrand’s Disease

DeBac, C.

HB_S and “e” Antigen-Antibody Systems in a Population of Hemophiliacs

de Cataldo, F.

The Use of Fibroseal in Hemophilic Cysts - A Case Report

De La Caffinière, J.Y.

Femoral Fractures in Severe Hemophilia

Delikaris, P.

Surgical Problems on Patients with Coagulation Defects

Delord, S.

Psychological Aspects of Training for home Treatment in Hemophilia

De Mitrio, V.

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Dentico, A.

Psychological Studies in Hemophiliacs in a Summer Camp

Dietrich, S.L.

Plasma Concentrate Consumption - A Five Year Study

Dietrich, Shelby L.

Long Term Results of Physical Therapy

Dodds, W.J.

A Family with an Unusual form of Factor VIII Deficiency

Autosomal Factor VIII Deficiency in Rabbits: Size Variations of Rabbit Factor VIII.

Dormandy, Katharine

The use of Ultrasonography in the Management of Haemophilia

Dreher, G.K.

A Family with an Unusual form of Factor VIII Deficiency

Duport, J.P.

“Santal” a Hemophiliac Data Bank in the Network Cyclades

Duthie, R.B.

Haemophilic Arthropathy - Ultrastructural and Microprobe Analysis

Duthie, Robert B.

Total Joint Replacement in the Hemophilias

Dzuback, J.

The All-American Blood Buddy: Donor Motivation for Hemophilia and Other Chronic Disorders

Eckenrode, J.W.

An Improved Method for Preparation of Antihemophilic Factor (AHF)

Edgington, T.

Multiple Molecular forms of Factor VIII Antigen in Normal Individuals and von Willebrand’s Disease Patients

Egeberg, O.

Hemophilia in Norway

Leukemia in Families with Isolated Cases of Severe Hemophilia A.

Elder, J.

Analysis of Bleeding Frequency in Hemophilia.

Elsinger, F.

Feiba Immuno: A Preparation with Factor Eight Inhibitor Bypassing Activity

Eqli, H.

Further Experience on the Effect of High Pre-Donation Factor VIII Levels in Blood Donors on the Factor VIII Content of Small-Pool Fractions

Etzel, F.

Home Care in Germany: Philosophy of Treatment, Results of Intensive Care

The Successful Treatment of Aquired Inhibitors Against Factor VIII.

Evans, Bruce E.

Case Histories

Oral Surgery and Dental Treatment for Hemophiliacs

Evans, R.K.

Hemophilia in a Chromosomal Female - An Extreme Example of Lyonization?

Evensen, S.A.

Home Therapy for Haemophilia in Norway: Effect on Transfusion Frequency and Absenteeism

Ewald, Brian A.

Elective Synovectomy in Hemophilia

Exner, T.

Factor VIII Deficient Plasma for Laboratory Tests Prepared from Normal Plasma and a Human Antibody

Conditions Contributing to the Stability of Factor VIII Coagulant Activity

Eyster, E.

Sgot Elevations and Hepatitis B Infections in Hemophiliacs

Eyster, M. Elaine

Particulate Material in Factor VIII Concentrates

Eyster, M.E.

Personality Characteristics of Hemophiliac Children

Collected Experience of the Pennsylvania Hemophilia Program

Effects of Psychiatric Intervention on Concentrate Usage

Comparison of Factor VIII Levels After Adrenalin IN Hemophilia a and von Willebrand’s Disease (VWD)

Farin, I.

A Laser Scalpel for Operations on Hemophiliacs

Farine, I.

A Method for Assessment and Grading of Osteoarthropathy in Hemophiliacs

Fass, D.N.

The Interaction of the Platelet and von Willebrand Factor

Fekete, L.F.

The Large Scale Preparation of Clottable Fibrinogen-Free, High Purity, High Potency Factor VIII Concentrate

Fernandez-Palazzi, F.

Nerve Lesions in Haemophilia

Radioactive Synoviorthesis in Haemophiliac Haemarthrosis

Ferrini, P. Rossi

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Fgli, H.

The Successful Treatment of Aquired Inhibitors Against Factor VIII.

Frommel, D.

“Santal” a Hemophiliac Data Bank in the Network Cyclades

Furlan, M.

Degradation of Factor VIII-Related Protein in Factor VIII Concentrates

Chemical Cross-Linking of Factor VIII Subunits

Gago, J.

Sinoviorthesis with AU-198 in 25 Cases of Hemophilic Arthropathy

Gazengel, C.

Antibody-Induced von Willebrand’s Disease. Dissociation of Factor VIII Molecular Complex Activities by the Autoantibody

George, R.

The Hemophiliac and Knowledge of Their Condition

An Evaluation of Hospital Facilities for Canadian Hemophiliacs

Gilbert, M.S.

Surgical Management and Complcations.

Gilhuus-Moe, C.

A Multicenter Evaluation of an Activated Partial Thromboplastin Time Test, Cepho-Test

Girot, R.

Antibody-Induced von Willebrand’s Disease. Dissociation of Factor VIII Molecular Complex Activities by the Autoantibody

Godal, H.C.

A Multicenter Evaluation of an Activated Partial Thromboplastin Time Test, Cepho-Test

Goldman, Donald

Legal Ways to Contest job Discrimination Among Hemophiliacs

Goldsmith, J.C.

Mutant forms of Factor IX

Golematis, B.

Surgical Problems on Patients with Coagulation Defects

Gomperts, E.D.

The Management of two Cases of “Spontaneous” Factor VIII Inhibitors with high Dose Cyclophosphamide

Gonzaga, A.L.

A Case of Henoch-Schoenlein Purpura in Hemophilia

Graham, John B.

Classifying Potential Carriers of Hemophilia: Report of the Joint WFH-WHO Expert Committee

Granich, B.

Psycho-Social Status of Patients on Home Care-6 Year Follow UP.

Green, D.

Head Trauma in Hemophilia: Value of Computer Tomography of The Brain in Localizing Multiple Hematomas

Grøan, K.

Home Therapy for Haemophilia in Norway: Effect on Transfusion Frequency and Absenteeism

Hall, C.A.

A Family with an Unusual form of Factor VIII Deficiency

Hammerling, J.

Analysis of Bleeding Frequency in Hemophilia.

Handelsman, J.E.

The Natural History of Haemophilic Arthritis

Harris, C.E.C.

The Natural History of “Inhibitors” to Factors VIII and IX in Hemophiliacs

Hasiba, Ute

Liver Disease in Hemophilia

Human Factor VIII Concentrates in Hemophiliac Dogs

Elevations in VIII:C, VIIIR:Ag and VIIIR:vW

Hasler, K.

Hemophilia a and Variant of von Willebrand’s Disease in one Family

Immunologic Studies in Patients with Von Willebrand’s Disease

Haverstick, J.

Sgot Elevations and Hepatitis B Infections in Hemophiliacs

Effects of Psychiatric Intervention on Concentrate Usage

Heim, M.

A Laser Scalpel for Operations on Hemophiliacs

A Method for Assessment and Grading of Osteoarthropathy in Hemophiliacs

Hildenbrand, Eqli H.

Home Care in Germany: Philosophy of Treatment, Results of Intensive Care

Hilgartner, M.W.

Psycho-Social Status of Patients on Home Care-6 Year Follow UP.

Hill, R.R.

The Natural History of Haemophilic Arthritis

Hiloartner, M.W.

Arterio-Venous Fistula to Facilitate Self Transfusion for the Hemophiliac

Hoffmann, P.

Home Care in Germany: Philosophy of Treatment, Results of Intensive Care

Hofmann, P.

Biomechanical Alterations Caused by Musculo’s Keletal Bleedings.

The Successful Treatment of Aquired Inhibitors Against Factor VIII.

Horoszowski, H.

A Summer Camp for Hemophilic Boys: A Film.

A Laser Scalpel for Operations on Hemophiliacs

A Method for Assessment and Grading of Osteoarthropathy in Hemophiliacs

Hossaini, A.

HB_sAg in Donors, Patients, Laboratory Personnel and Housestaff of a Military Hospital in IRAQ: A Seroepidemiologic Study

Hummel, L.

School Attendance Pre and Post Home Infusion Therapy

Ingram, G.I.C.

An Artificial ‘Haemophilic’ Plasma for One-Stage Factor VIII Assay

Inwood, M.J.

The Need to Filter Cryoprecipitate. A Microscopic Assessment of Filter Deposition

Effect of Ibuprofen on Platelet Function in Normal Subjects and Hemophiliacs

The Hemophiliac and Knowledge of Their Condition

An Evaluation of Hospital Facilities for Canadian Hemophiliacs

A Comparison of Current Prophylactic Therapy in Canada and the United Kingdom

Iwakura, H.

Defibrination Syndrome Developed after Replacement Therapy with PPSB in a Case of Hemophilia B.

Jacques, C.

Antibody-Induced von Willebrand’s Disease. Dissociation of Factor VIII Molecular Complex Activities by the Autoantibody

Jakab, T.

Degradation of Factor VIII-Related Protein in Factor VIII Concentrates

Chemical Cross-Linking of Factor VIII Subunits

Jewett, Warren R.

Improved Factor VIII Yield by Instrumented Cryo-Precipitate Harvesting Technique

Jonas, D.L.

Mental Health Collaboration in a Comprehensive Care Team

Josso, F.

Antibody-Induced von Willebrand’s Disease. Dissociation of Factor VIII Molecular Complex Activities by the Autoantibody

Kaegi, A.

Activated Prothrombin Concentrates in Management of Bleeding in a Classical Hemophiliac with Inhibitor

Karim, S.

HB_sAg in Donors, Patients, Laboratory Personnel and Housestaff of a Military Hospital in IRAQ: A Seroepidemiologic Study

Kasper, C.K.

Plasma Concentrate Consumption - A Five Year Study

Kassira, E.

HB_sAg in Donors, Patients, Laboratory Personnel and Housestaff of a Military Hospital in IRAQ: A Seroepidemiologic Study

Kazama, M.

Defibrination Syndrome Developed after Replacement Therapy with PPSB in a Case of Hemophilia B.

Kelly, P.

Factor VIII Inhibitors: Therapeutic Response to Prothrombin Complex Concentrates

Michigan’s Summer camp for Hemophiliacs

Low Dose Factor Replacement in the Hemophiliac

Kelly, P.E.

Surgery in Hemophilic Patients with Inhibitors

Kimball, J.

Multiple Molecular forms of Factor VIII Antigen in Normal Individuals and von Willebrand’s Disease Patients

Kingdon, H.S.

Recent Reduction in Thrombogenic Enzyme Content of Prothrombin Complex Concentrates

Klatsky, A.U.

Recurrent Acute Hepatitis Following the Use of Antihemophilic Factor Concentrates

Kopicki, John

The Role of the Consumer-Patient in the Growth of a Comprehensive Hemophilia Care Unit

Köves, Á

Diagnostic and Therapeutic Problems in a Patient with Factor VIII Inhibitor

Kronenberg, H.

Factor VIII Deficient Plasma for Laboratory Tests Prepared from Normal Plasma and a Human Antibody

Conditions Contributing to the Stability of Factor VIII Coagulant Activity

Kun, L.

Diagnostic and Therapeutic Problems in a Patient with Factor VIII Inhibitor

Larrieu, M.J.

Femoro-Patellar Syndrome in Hemophilic Knee

Laurian, Y.

Femoral Fractures in Severe Hemophilia

Femoro-Patellar Syndrome in Hemophilic Knee

Lee, Helen

Large Scale Purification and Characterisation of Porcine Factor VIII for Clinical Use

Legnaioli, M.

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Levine, P.H.

Hemophilic Arthropathy in the Home Care Setting

Factor IX Related Antigen in Hemophllia B

Lewis, B.

Current Organization of General Dental Programs for Hemophiliacs

Lewis, J.

Collected Experience of the Pennsylvania Hemophilia Program

Lewis, J.C.

The Interaction of the Platelet and von Willebrand Factor

Lewis, Jessica H.

Liver Disease in Hemophilia

Human Factor VIII Concentrates in Hemophiliac Dogs

Elevations in VIII:C, VIIIR:Ag and VIIIR:vW

Ley, C.

Convenient Microtiter assay for von Willebrand’s Factor

Lian, E.C.Y.

Factor 8 Activity in a Hemophiliac Patient with Acute Lymphocytic Leukemia

Lipton, R.

The Role of the Dental Hygienist in a Community Hospital Hemophilia Program

Lipton, R.A.

A Computer Analysis of Patient Activity and Blood Product Usage in Community Hospital Hemophilia Program

Locchi, F.

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Loizou, C.

Surgical Problems on Patients with Coagulation Defects

Lotz, L.

Observations on a Change from “Altruistic” to” “Assurance” Blood Donors

Lovrien, E.W.

Analysis of Bleeding Frequency in Hemophilia.

Lurie, A.L.

The Natural History of Haemophilic Arthritis

Lusher, J.M.

Hemophilia in a Chromosomal Female - An Extreme Example of Lyonization?

Michigan’s Summer camp for Hemophiliacs

Mackay, S. Ross

Prophylaxis for Hemophilic Arthropathy

Magall, M.

Sinoviorthesis with AU-198 in 25 Cases of Hemophilic Arthropathy

Mandalaki, T.

Surgical Problems on Patients with Coagulation Defects

Mannucci, P.M.

A Multicenter Evaluation of an Activated Partial Thromboplastin Time Test, Cepho-Test

Significance of Abnormal Liver Function Tests in Hemophiliacs: A Follow-Up Study

Synovectomy Revisited

Mannucoi, P.M.

A National Reference Curve for Assaying Factor VIII Inhibitors

Mariani, G.

A National Reference Curve for Assaying Factor VIII Inhibitors

HB_S and “e” Antigen-Antibody Systems in a Population of Hemophiliacs

Martinson, A.M.

Elbow Arthroplasty in Hemophilic Arthritis

Martin-Villar, J.

Sinoviorthesis with AU-198 in 25 Cases of Hemophilic Arthropathy

Mazzucconi, M.G.

HB_S and “e” Antigen-Antibody Systems in a Population of Hemophiliacs

McAuley, Clyde B.

Hepatitis B Surface Antigen Testing in Plasmapheresis Donors

McIntyre, B.A.

Effect of Ibuprofen on Platelet Function in Normal Subjects and Hemophiliacs

McLone, D.

Head Trauma in Hemophilia: Value of Computer Tomography of The Brain in Localizing Multiple Hematomas

McVerry, B.A.

Hemophilic Arthropathy in the Home Care Setting

The use of Ultrasonography in the Management of Haemophilia

McWilliams, N.B.

Home Treatment for Children with Hemophilia

Melo, G. O. S. de

Factor VIII and Factor VIII Related Antigen in Normal Pregnancy

Mercer, J.E.

An Improved Method for Preparation of Antihemophilic Factor (AHF)

Meyer, S.C.

Factor 8 Activity in a Hemophiliac Patient with Acute Lymphocytic Leukemia

Miller, Merrill

The Aspirin Bleeding Time - A Screening Test for Evaluation of von Willebrand’s Disease

Morfini, M.

Nitro Bleu Tetrazolium Reduction test in Hemophilia

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Morrison, F.S.

Observations on a Change from “Altruistic” to” “Assurance” Blood Donors

Mulkey, T.F.

Evaluation and Approach to Indicated Oral Surgery

Myers, Marilyn G.

Elective Synovectomy in Hemophilia

Nakajima, M.

Defibrination Syndrome Developed after Replacement Therapy with PPSB in a Case of Hemophilia B.

Nau, Martin E.

Particulate Material in Factor VIII Concentrates

Nilsson, I.M.

A Multicenter Evaluation of an Activated Partial Thromboplastin Time Test, Cepho-Test

Noël, B.

“Santal” a Hemophiliac Data Bank in the Network Cyclades

Olness, K.N.

Effects of Self Hypnosis in the Management of Hemophilia in Children

Oreste, A.

Feasibility of Antifibrinolytic Treatment in Hemophilia: Preliminary Study

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Ortega, F.

Sinoviorthesis with AU-198 in 25 Cases of Hemophilic Arthropathy

Ownby, R.

Home Treatment for Children with Hemophilia

O’Connell, F.D.

Hemophilic Arthropathy in the Home Care Setting

Páez, C.A.

Haemophilia Therapy: A View from the Third World

Pander, U.

Factor VIII Associated Antigen, Platelet Retention and Platelet Aggregation in Patients with Vascular Diseases

Panicucci, F.

Four Years’ Follow-Up Study of Liver Function of Haemophiliacs

Electroimmunoassay of Factor IX in the Detection of Haemophilia B Carriers

Papalabros, E.

Surgical Problems on Patients with Coagulation Defects

Pareti, F.

Significance of Abnormal Liver Function Tests in Hemophiliacs: A Follow-Up Study

Pasqual Marsettin, E.

Psychological Studies in Hemophiliacs in a Summer Camp

Pavlovsky, A.

Bovine Factor VIII. Antigens and Biological Activities

Penner, J.

Low Dose Factor Replacement in the Hemophiliac

Penner, J.A.

Hemophilia in a Chromosomal Female - An Extreme Example of Lyonization?

Michigan’s Summer camp for Hemophiliacs

Surgery in Hemophilic Patients with Inhibitors

Permer, J.

Factor VIII Inhibitors: Therapeutic Response to Prothrombin Complex Concentrates

Petö, I.

Diagnostic and Therapeutic Problems in a Patient with Factor VIII Inhibitor

Petronelli, M.

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Pflugshaupt, R.

Degradation of Factor VIII-Related Protein in Factor VIII Concentrates

Philp, R.B.

Effect of Ibuprofen on Platelet Function in Normal Subjects and Hemophiliacs

Pietrogrande, V.

Synovectomy Revisited

Pinori, E.

Electroimmunoassay of Factor IX in the Detection of Haemophilia B Carriers

Plotkin, S.

Sgot Elevations and Hepatitis B Infections in Hemophiliacs

Prager, D.

Comparison of Factor VIII Levels After Adrenalin IN Hemophilia a and von Willebrand’s Disease (VWD)

Prieur, A.M.

Antibody-Induced von Willebrand’s Disease. Dissociation of Factor VIII Molecular Complex Activities by the Autoantibody

Refsum, N.

A Multicenter Evaluation of an Activated Partial Thromboplastin Time Test, Cepho-Test

Rickard, K.A.

Factor VIII Deficient Plasma for Laboratory Tests Prepared from Normal Plasma and a Human Antibody

Conditions Contributing to the Stability of Factor VIII Coagulant Activity

Rickles, F.R.

Recurrent Acute Hepatitis Following the Use of Antihemophilic Factor Concentrates

Ripa, T.

Feasibility of Antifibrinolytic Treatment in Hemophilia: Preliminary Study

Psychological Studies in Hemophiliacs in a Summer Camp

Rippey, J.J.

The Natural History of Haemophilic Arthritis

Rivas, M.

Analysis of Bleeding Frequency in Hemophilia.

Roberts, H.R.

Mutant forms of Factor IX

Rossi Ferrini, P.

Nitro Bleu Tetrazolium Reduction test in Hemophilia

Rüdel, J.

Results of Liver Biopsies, Rate of Icteric Hepatitis, and Frequency of Anti-HBs and Hbs-Antigen in Patients of the Heidelberg Hemophilia Center

Ruggeri, Z.M.

A National Reference Curve for Assaying Factor VIII Inhibitors

Significance of Abnormal Liver Function Tests in Hemophiliacs: A Follow-Up Study

Platelets, Endothelial Cells and von Willebrand Factor

Synovectomy Revisited

Sachs, S.

The Role of the Dental Hygienist in a Community Hospital Hemophilia Program

Sachs, S.A.

Alternatives to oral Surgery for Hemophiliacs

Sagripanti, A.

Four Years’ Follow-Up Study of Liver Function of Haemophiliacs

Electroimmunoassay of Factor IX in the Detection of Haemophilia B Carriers

Saint Paul, E.

“Santal” a Hemophiliac Data Bank in the Network Cyclades

Salti, F.

Nitro Bleu Tetrazolium Reduction test in Hemophilia

Sas, G.

Diagnostic and Therapeutic Problems in a Patient with Factor VIII Inhibitor

Scaraggi, F.

Psychological Studies in Hemophiliacs in a Summer Camp

Scaraggi, F.A.

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Scaraggi, F A.

Feasibility of Antifibrinolytic Treatment in Hemophilia: Preliminary Study

Schachter, M.

The Role of the Dental Hygienist in a Community Hospital Hemophilia Program

Scharrer, I.

Factor VIII Associated Antigen, Platelet Retention and Platelet Aggregation in Patients with Vascular Diseases

Clinical Results of Synovectomies and Other Orthopedic Corrective Surgery in Patients with Hemophilia A and B

Schiavoni, M.

Feasibility of Antifibrinolytic Treatment in Hemophilia: Preliminary Study

Von Willebrand Disease Combined with Factor V Deficiency: Variant Bari

Schiff, P.

The Problem. How Much is Required?

Schimpf, Kl.

Replacement Therapy with a Factor VII Concentrate in Severe Factor VII Deficiency

Results of Liver Biopsies, Rate of Icteric Hepatitis, and Frequency of Anti-HBs and Hbs-Antigen in Patients of the Heidelberg Hemophilia Center

Treatment of Joint-Bleedings in Hemophiliacs with Antibodies to Factor VIII with High doses of Fraction Feiba.

Schorn, P.

Application of the Partial Thromboplastin time for Diagnosis and Treatment of Hemophilia

Schumpe, G.

Biomechanical Alterations Caused by Musculo’s Keletal Bleedings.

Seligsohn, U.

A Summer Camp for Hemophilic Boys: A Film.

A Laser Scalpel for Operations on Hemophiliacs

A Method for Assessment and Grading of Osteoarthropathy in Hemophiliacs

Serbanescu, F.

A National Reference Curve for Assaying Factor VIII Inhibitors

Seri, A.

Nitro Bleu Tetrazolium Reduction test in Hemophilia

Shapiro, S.S.

Preliminary Report of the Cooperative Study of Spontaneously Occuring Factor VIII Inhibitors in Patients with Hemophilia

Collected Experience of the Pennsylvania Hemophilia Program

Silvello, L.

The Use of Fibroseal in Hemophilic Cysts - A Case Report

Silverman, M.A.

Factor 8 Activity in a Hemophiliac Patient with Acute Lymphocytic Leukemia

Simonetti, C.

Bovine Factor VIII. Antigens and Biological Activities

Singher, L.J.

Effects of Self Hypnosis in the Management of Hemophilia in Children

Sistemi, S.

Radioiron Uptake in Hemophiliacs Joints by 59FE-Red Cells Radioactivity Surface Counting

Spero, Joel A.

Liver Disease in Hemophilia

Human Factor VIII Concentrates in Hemophiliac Dogs

Elevations in VIII:C, VIIIR:Ag and VIIIR:vW

Stapp, W.F.

Oral Prophylactic Therapy in Hemophilia A and B (Factor VIII and IX Deficiencies)

Stein, H.

Haemophilic Arthropathy - Ultrastructural and Microprobe Analysis

Strickler, E.

Personality Characteristics of Adult Hemophiliacs

Strickler, E.M.

Clinical Severity, Personality Characteristics and Maternal Attitudes in Hemophiliac Children

Stuart, Marie J.

The Aspirin Bleeding Time - A Screening Test for Evaluation of von Willebrand’s Disease

Stubenbord, W.T.

Arterio-Venous Fistula to Facilitate Self Transfusion for the Hemophiliac

Sutor, A.H.

Hemophilia a and Variant of von Willebrand’s Disease in one Family

Application of the Partial Thromboplastin time for Diagnosis and Treatment of Hemophilia

Immunologic Studies in Patients with Von Willebrand’s Disease

Sweet, M.B.E.

The Natural History of Haemophilic Arthritis

Taliani, G.

HB_S and “e” Antigen-Antibody Systems in a Population of Hemophiliacs

Tembrevilla-Zubiri, C.L.

Recurrent Acute Hepatitis Following the Use of Antihemophilic Factor Concentrates

Thamer, G.

Results of Liver Biopsies, Rate of Icteric Hepatitis, and Frequency of Anti-HBs and Hbs-Antigen in Patients of the Heidelberg Hemophilia Center

Thaule, R.

Home Therapy for Haemophilia in Norway: Effect on Transfusion Frequency and Absenteeism

Thompson, F.

The All-American Blood Buddy: Donor Motivation for Hemophilia and Other Chronic Disorders

Thonar, E.J-M.A.

The Natural History of Haemophilic Arthritis

Tilburg, N.H. van

Carrier Detection in Hemophilia B.

Tomic, D.

Hemostasis in the Oral Cavity

Torri, G.

Synovectomy Revisited

Troner, M.B.

Factor 8 Activity in a Hemophiliac Patient with Acute Lymphocytic Leukemia

Tsigris, Ch.

Surgical Problems on Patients with Coagulation Defects

Underwood, S.

Analysis of Bleeding Frequency in Hemophilia.

VanHarlingen, D.

The All-American Blood Buddy: Donor Motivation for Hemophilia and Other Chronic Disorders

VanHarlingen, David

Hemophilia: A Moral Dilemma

The Role of the Consumer-Patient in the Growth of a Comprehensive Hemophilia Care Unit

Vaudreuil, C.

Fluctuations in Factor VIII Procoagulant, Antigen and Von Willebrand Factor in Normal Individuals

Veltkamp, J.J.

Carrier Detection in Hemophilia B.

Factor IX Level in Various Conditions

Verrecchio, J.

Personality Characteristics of Hemophiliac Children

Clinical Severity, Personality Characteristics and Maternal Attitudes in Hemophiliac Children

Vicary, F.R.

The use of Ultrasonography in the Management of Haemophilia

Vinazzer, H.

Experimental Studies on Factor VIII Inhibitor Bypassing Activity

Voke, Jennifer

The use of Ultrasonography in the Management of Haemophilia

Warren, B.A.

The Need to Filter Cryoprecipitate. A Microscopic Assessment of Filter Deposition

Warrier, I.

Hemophilia in a Chromosomal Female - An Extreme Example of Lyonization?

Weinberg, P.

Head Trauma in Hemophilia: Value of Computer Tomography of The Brain in Localizing Multiple Hematomas

Weissman, Jerry

A Demonstration of Physical Therapy

Weksler, B.B.

Convenient Microtiter assay for von Willebrand’s Factor

Whaun, J.M.

Activated Prothrombin Concentrates in Management of Bleeding in a Classical Hemophiliac with Inhibitor

Wickerhauser, M.

An Improved Method for Preparation of Antihemophilic Factor (AHF)

Willert, H.G.

Clinical Results of Synovectomies and Other Orthopedic Corrective Surgery in Patients with Hemophilia A and B

Wilson, W.L.

The Large Scale Preparation of Clottable Fibrinogen-Free, High Purity, High Potency Factor VIII Concentrate

Wincott, E.

Mental Health Collaboration in a Comprehensive Care Team

Wolk, Joel

The Aspirin Bleeding Time - A Screening Test for Evaluation of von Willebrand’s Disease

Woods, William

Improved Factor VIII Yield by Instrumented Cryo-Precipitate Harvesting Technique

Yang, H.C.

Fluctuations in Factor VIII Procoagulant, Antigen and Von Willebrand Factor in Normal Individuals

Factor IX Related Antigen in Hemophllia B

Zeltsch, P.

Results of Liver Biopsies, Rate of Icteric Hepatitis, and Frequency of Anti-HBs and Hbs-Antigen in Patients of the Heidelberg Hemophilia Center

Treatment of Joint-Bleedings in Hemophiliacs with Antibodies to Factor VIII with High doses of Fraction Feiba.

Zimbler, S.

Hemophilic Arthropathy in the Home Care Setting

Zimbler, Seymour

Surgery in Hemophilia

Zimmerman, T.

Multiple Molecular forms of Factor VIII Antigen in Normal Individuals and von Willebrand’s Disease Patients

Zimmermann, K.

Replacement Therapy with a Factor VII Concentrate in Severe Factor VII Deficiency

Results of Liver Biopsies, Rate of Icteric Hepatitis, and Frequency of Anti-HBs and Hbs-Antigen in Patients of the Heidelberg Hemophilia Center

Treatment of Joint-Bleedings in Hemophiliacs with Antibodies to Factor VIII with High doses of Fraction Feiba.

Zottoli, Carolyn

A Demonstration of Physical Therapy