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Congenital deficiency of vitamin K-dependent coagulation factors associated with central nervous system anomalies

Thrombosis and haemostasis, 2004-04, Vol.91 (4), p.819-821

2004

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Use of recombinant factor VIIa to control bleeding in an adolescent male with severe hemophilia A, HIV, thrombocytopenia, hepatitis C, and end-stage liver disease

American journal of hospice & palliative medicine, 2002-07, Vol.19 (4), p.277-282

2002

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Inhibition of Thymopoiesis of CD34+ Cell Maturation by HIV‐1 in an In Vitro CD34+ Cell and Thymic Epithelial Organ Culture Model

Stem cells (Dayton, Ohio), 1999-01, Vol.17 (6), p.327-338

1999

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Use of recombinant factor vila to control bleeding in an adolescent male with severe hemophilia A, HIV thrombocytopenia, hepatitis C, and end-stage liver disease

American journal of hospice & palliative medicine, 2002-07, Vol.19 (4), p.277-282

2002

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Management of von Willebrand disease: a survey on current clinical practice from the haemophilia centres of North America

Haemophilia : the official journal of the World Federation of Hemophilia, 2001-05, Vol.7 (3), p.235-241

2001

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Abnormal in vitro thymocyte differentiation in a patient with severe combined immunodeficiency-Nezelof's syndrome

Journal of clinical immunology, 1996-05, Vol.16 (3), p.151-158

1996

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T Cell Differentiation/Maturation of CD34+ Stem Cells from HIV‐Seropositive Hemophiliacs in Cultured Thymic Epithelial Fragments

Stem cells (Dayton, Ohio), 1996-01, Vol.14 (1), p.132-145

1996

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Arrest of In Vitro T Cell Differentiation of Normal Bone Marrow‐Derived CD34+ Stem Cells with Thymic Epithelial Fragments from Children with AIDS

Stem cells (Dayton, Ohio), 1996-09, Vol.14 (5), p.533-547

1996

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Development of a Method of Thymocyte Differentiation of Bone Marrow‐Enriched CD34+CD38− Cells in Postnatal Allogeneic Cultured Thymic Epithelia to Evaluate Immunodeficiency Disorders

Stem cells (Dayton, Ohio), 1996-11, Vol.14 (6), p.702-713

1996

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Abnormalin vitro thymocyte differentiation in a patient with severe combined immunodeficiency-Nezelof's syndrome

Journal of clinical immunology, 1996-05, Vol.16 (3), p.151-158

1996

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Conservative management of spinal epidural hematoma in hemophilia

Pediatric neurology, 1988-05, Vol.4 (3), p.169-171

1988

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Aortic valve replacement in von Willebrand's disease

The Journal of thoracic and cardiovascular surgery, 1978-08, Vol.76 (2), p.218-222

1978

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Thymosin- α 1 stimulates maturation of CD34+ stem cells into CD3+4+ cells in an in vitro thymic epithelia organ coculture model

International journal of immunopharmacology, 1999-01, Vol.21 (1), p.15-26

1999

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HTLV-III/LAV Antibody Status of Spouses and Household Contacts Assisting in Home Infusion of Hemophilia Patients

Blood, 1985-09, Vol.66 (3), p.703-705

1985

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792 FACTOR VIII INHIBITOR RESPONSE TO CYCLOPHOSPHAMIDE (C)

Pediatric research, 1981-04, Vol.15, p.574-574

1981

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Factor XIII deficiency: Concentrations inrelatives of patients and in normal infants

The Journal of pediatrics, 1968, Vol.72 (3), p.336-341

1968

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PURPURA FULMINANS

Pediatrics (Evanston), 1964-08, Vol.34 (2), p.264-270

BOUHASIN, J D

1964

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Classic hemophilia A in a female

Acta haematologica, 1977-01, Vol.58 (2), p.94-102

1977

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51 Factor XIII-Report of a Family with Factor XIII Deficiency and the Concentrations in normal Infants

Pediatric research, 1967-05, Vol.1 (3), p.213-213

1967

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AIDS in a Hemophiliac Child Transmitted by Cryoprecipitate and with Negative HIV Antibodies by Western Blot

Pediatric asthma, allergy & immunology, 1990, Vol.4 (2), p.141-146

1990

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Role of the lymphocyte in antihemophilic globulin production: a rise in antihemophilic globulin levels in a hemophilic subject with acute lymphoblastic leukemia

The Journal of laboratory and clinical medicine, 1971-07, Vol.78 (1), p.122

1971

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Chronic idiopathic thrombocytopenic purpura followed by chronic myelocytic leukemia

The American journal of pediatric hematology/oncology, 1981, Vol.3 (1), p.83

1981

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Combination therapy with ribavirin and interferon in a cohort of children with hepatitis C and haemophilia followed at a pediatric haemophilia treatment center

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-01, Vol.10 (1), p.87-93

2004

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Congenital deficiency of vitamin K-dependent coagulation factors associated with central nervous system anomalies

Use of recombinant factor VIIa to control bleeding in an adolescent male with severe hemophilia A, HIV, thrombocytopenia, hepatitis C, and end-stage liver disease

Inhibition of Thymopoiesis of CD34+ Cell Maturation by HIV‐1 in an In Vitro CD34+ Cell and Thymic Epithelial Organ Culture Model

Use of recombinant factor vila to control bleeding in an adolescent male with severe hemophilia A, HIV thrombocytopenia, hepatitis C, and end-stage liver disease

Management of von Willebrand disease: a survey on current clinical practice from the haemophilia centres of North America

Abnormal in vitro thymocyte differentiation in a patient with severe combined immunodeficiency-Nezelof's syndrome

T Cell Differentiation/Maturation of CD34+ Stem Cells from HIV‐Seropositive Hemophiliacs in Cultured Thymic Epithelial Fragments

Arrest of In Vitro T Cell Differentiation of Normal Bone Marrow‐Derived CD34+ Stem Cells with Thymic Epithelial Fragments from Children with AIDS

Development of a Method of Thymocyte Differentiation of Bone Marrow‐Enriched CD34+CD38− Cells in Postnatal Allogeneic Cultured Thymic Epithelia to Evaluate Immunodeficiency Disorders

Abnormalin vitro thymocyte differentiation in a patient with severe combined immunodeficiency-Nezelof's syndrome

Conservative management of spinal epidural hematoma in hemophilia

Aortic valve replacement in von Willebrand's disease

Thymosin- α 1 stimulates maturation of CD34+ stem cells into CD3+4+ cells in an in vitro thymic epithelia organ coculture model

HTLV-III/LAV Antibody Status of Spouses and Household Contacts Assisting in Home Infusion of Hemophilia Patients

792 FACTOR VIII INHIBITOR RESPONSE TO CYCLOPHOSPHAMIDE (C)

Factor XIII deficiency: Concentrations inrelatives of patients and in normal infants

PURPURA FULMINANS

Classic hemophilia A in a female

51 Factor XIII-Report of a Family with Factor XIII Deficiency and the Concentrations in normal Infants

AIDS in a Hemophiliac Child Transmitted by Cryoprecipitate and with Negative HIV Antibodies by Western Blot

Role of the lymphocyte in antihemophilic globulin production: a rise in antihemophilic globulin levels in a hemophilic subject with acute lymphoblastic leukemia

Chronic idiopathic thrombocytopenic purpura followed by chronic myelocytic leukemia

Combination therapy with ribavirin and interferon in a cohort of children with hepatitis C and haemophilia followed at a pediatric haemophilia treatment center

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