Bertil Glader

Pathologist, Hematopathologist

Professor of Pediatrics (Hematology/Oncology) and, by courtesy, of Pathology

Professional Education

Board Certification: Pediatrics, American Board of Pediatrics (1982)

Fellowship: Children's Hospital Boston (1974) MA

Residency: Children's Hospital Boston (1973) MA

Board Certification: Pediatric Hematology-Oncology, American Board of Pediatrics (1982)

Board Certification: Hematology, American Board of Pathology (1983)

Internship: Stanford University School of Medicine (1969) CA

Medical Education: Northwestern University Medical School (1968) IL

BA, Northwestern University, Philosophy (1961)

PhD, University of Illinois, Physiology (1967)

MD, Northwestern University, Medicine (1968)

Administrative Appointments

Professor of Pediatrics, Stanford University (1987 - Present)

Associate Professor of Pediatrics, Stanford University (1977 - 1987)

Assistant Professor of Pediatrics, Harvard Medical School (1974 - 1977)

Instructor in Pediatrics, Harvard Medical School (1973 - 1974)

Clinical Trials

Clinical trials are research studies that evaluate a new medical approach, device, drug, or other treatment. As a Stanford Health Care patient, you may have access to the latest, advanced clinical trials.

Open trials refer to studies currently accepting participants. Closed trials are not currently enrolling, but may open in the future.

Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia
Landowski, M., O'Donohue, M.-F., Buros, C., Ghazvinian, R., Montel-Lehry, N., & Gazda, H. T. (2013). Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia. HUMAN GENETICS, 132(11), 1265-1274.

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
Andolfo, I., Alper, S. L., De Franceschi, L., Auriemma, C., Russo, R., & Iolascon, A. (2013). Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1. Blood, 121(19), 3925-?.

Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia
Gazda, H. T., Preti, M., Sheen, M. R., O'Donohue, M.-F., Vlachos, A., & Beggs, A. H. (2012). Frameshift mutation in p53 regulator RPL26 is associated with multiple physical abnormalities and a specific pre-ribosomal RNA processing defect in diamond-blackfan anemia. HUMAN MUTATION, 33(7), 1037-1044.

Adenovirus-Associated Virus Vector-Mediated Gene Transfer in Hemophilia B
Nathwani, A. C., Tuddenham, E. Gd., Rangarajan, S., Rosales, C., McIntosh, J., & Davidoff, A. M. (2011). Adenovirus-Associated Virus Vector-Mediated Gene Transfer in Hemophilia B. NEW ENGLAND JOURNAL OF MEDICINE, 365(25), 2357-2365.

Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome
McGowan, K. A., Pang, W. W., Bhardwaj, R., Perez, M. G., Pluvinage, J. V., & Barsh, G. S. (2011). Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome. BLOOD, 118(13), 3622-3633.

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
Stewart, A. K., Kedar, P. S., Shmukler, B. E., Vandorpe, D. H., Hsu, A., & Alper, S. L. (2011). Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 300(5), C1034-C1046.

Development of Antibodies to Human Thrombin and Factor V in a Patient Exposed to Topical Bovine Thrombin
Lo, C. Y., Jones, C., Glader, B., & Zehnder, J. L. (2010). Development of Antibodies to Human Thrombin and Factor V in a Patient Exposed to Topical Bovine Thrombin. PEDIATRIC BLOOD & CANCER, 55(6), 1195-1197.

Adrenal and renal corticomedullary junction iron deposition in red cell aplasia
Rakow-Penner, R., Glader, B., Yu, H., & Vasanawala, S. (2010). Adrenal and renal corticomedullary junction iron deposition in red cell aplasia. PEDIATRIC RADIOLOGY, 40(12), 1955-1957.

Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia
Doherty, L., Sheen, M. R., Vlachos, A., Choesmel, V., O'Donohue, M.-F., & Gazda, H. T. (2010). Ribosomal Protein Genes RPS10 and RPS26 Are Commonly Mutated in Diamond-Blackfan Anemia. AMERICAN JOURNAL OF HUMAN GENETICS, 86(2), 222-228.

Monthly recombinant tissue plasminogen activator administration to implantable central venous access devices decreases infections in children with haemophilia
Jeng, M. R., O'Brien, M., Wong, W., Zoland, J., Lea, J., & Glader, B. (2009). Monthly recombinant tissue plasminogen activator administration to implantable central venous access devices decreases infections in children with haemophilia. HAEMOPHILIA, 15(6), 1272-1280.

One Year Follow-Up of Children and Adolescents With Chronic Immune Thrombocytopenic Purpura (ITP) Treated With Rituximab
Mueller, B. U., Bennett, C. M., Feldman, H. A., Bussel, J. B., Abshire, T. C., & Neufeld, E. J. (2009). One Year Follow-Up of Children and Adolescents With Chronic Immune Thrombocytopenic Purpura (ITP) Treated With Rituximab. PEDIATRIC BLOOD & CANCER, 52(2), 259-262.

Ribosomal Protein L5 and L11 Mutations Are Associated with Cleft Palate and Abnormal Thumbs in Diamond-Blackfan Anemia Patients
Gazda, H. T., Sheen, M. R., Vlachos, A., Choesmel, V., O'Donohue, M.-F., & Beggs, A. H. (2008). Ribosomal Protein L5 and L11 Mutations Are Associated with Cleft Palate and Abnormal Thumbs in Diamond-Blackfan Anemia Patients. AMERICAN JOURNAL OF HUMAN GENETICS, 83(6), 769-780.

Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference
Vlachos, A., Ball, S., Dahl, N., Alter, B. P., Sheth, S., & Lipton, J. M. (2008). Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference. BRITISH JOURNAL OF HAEMATOLOGY, 142(6), 859-876.

Cold agglutinin syndrome in pediatric liver transplant recipients
Wong, W., Merker, J. D., Nguyen, C., Berquist, W., Jeng, M., & Fontaine, M. J. (2007). Cold agglutinin syndrome in pediatric liver transplant recipients. PEDIATRIC TRANSPLANTATION, 11(8), 931-936.

Ribosomal protein S24 gene is mutated in diamond-blackfan anemia
Gazda, H. T., Grabowska, A., Merida-Long, L. B., Latawiec, E., Schneider, H. E., & Sieff, C. A. (2006). Ribosomal protein S24 gene is mutated in diamond-blackfan anemia. AMERICAN JOURNAL OF HUMAN GENETICS, 79(6), 1110-1118.

Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura
Bennett, C. M., Rogers, Z. R., Kinnamon, D. D., Bussel, J. B., Mahoney, D. H., & Neufeld, E. J. (2006). Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura. BLOOD, 107(7), 2639-2642.

Successful transduction of liver in hemophilia by AAV-factor IX and limitations imposed by the host immune response
Manno, C. S., Arruda, V. R., Pierce, G. F., Glader, B., Ragni, M., & Kay, M. A. (2006). Successful transduction of liver in hemophilia by AAV-factor IX and limitations imposed by the host immune response. NATURE MEDICINE, 12(3), 342-347.

AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
Manno, C. S., Chew, A. J., Hutchison, S., Larson, P. J., Herzog, R. W., & Glader, B. (2003). AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B. BLOOD, 101(8), 2963-2972.

Approach to the bleeding child
Allen, G. A., & Glader, B. (2002). Approach to the bleeding child. PEDIATRIC CLINICS OF NORTH AMERICA, 49(6), 1239-?.

Resolution of severe Donath-Landsteiner autoimmune hemolytic anemia temporally associated with institution of plasmapheresis
Roy-Burman, A., & Glader, B. E. (2002). Resolution of severe Donath-Landsteiner autoimmune hemolytic anemia temporally associated with institution of plasmapheresis. CRITICAL CARE MEDICINE, 30(4), 931-934.

Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia
Gripp, K. W., McDonald-McGinn, D. M., La Rossa, D., McGain, D., Federman, N., & Zackai, E. H. (2001). Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia. AMERICAN JOURNAL OF MEDICAL GENETICS, 101(3), 268-274.

Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease
Gazda, H., Lipton, J. M., Willig, T. N., Ball, S., Niemeyer, C. M., & Sieff, C. A. (2001). Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease. BLOOD, 97(7), 2145-2150.

Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector
Kay, M. A., Manno, C. S., Ragni, M. V., Larson, P. J., Couto, L. B., & High, K. A. (2000). Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector. NATURE GENETICS, 24(3), 257-261.

Hemolytic anemia in children
Glader, B. E. (1999). Hemolytic anemia in children. CLINICS IN LABORATORY MEDICINE, 19(1), 87-?.

Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors
Key, N. S., Aledort, L. M., BEARDSLEY, D., Cooper, H. A., Davignon, G., & Taft, E. (1998). Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors. THROMBOSIS AND HAEMOSTASIS, 80(6), 912-918.

Bone marrow transplant in thalassemia - A role for radiation?
Lee, Y. S., Kristovich, K. M., Ducore, J. M., Vichinsky, E., Crouse, V. L., & Amylon, M. D. (1998). Bone marrow transplant in thalassemia - A role for radiation?. COOLEYS ANEMIA, 850, 503-505.

Acute idiopathic thrombocytopenic purpura - Management in childhood
Buchanan, G. R., deAlarcon, P. A., Feig, S. A., Gilchrist, G. S., Lukens, J. N., & Lusher, J. M. (1997). Acute idiopathic thrombocytopenic purpura - Management in childhood. BLOOD, 89(4), 1464-1465.

Loss of elbow and wrist motion in hemophilia
Gamble, J. G., Vallier, H., Rossi, M., & Glader, B. (1996). Loss of elbow and wrist motion in hemophilia. CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, (328), 94-101.

Hematologic disorders in children from Southeast Asia
Glader, B. E., & Look, K. A. (1996). Hematologic disorders in children from Southeast Asia. PEDIATRIC CLINICS OF NORTH AMERICA, 43(3), 665-?.

FREQUENCY OF INHIBITOR DEVELOPMENT IN HEMOPHILIACS TREATED WITH LOW-PURITY FACTOR-VIII
Addiego, J., Kasper, C., Abildgaard, C., Hilgartner, M., Lusher, J., & Aledort, L. (1993). FREQUENCY OF INHIBITOR DEVELOPMENT IN HEMOPHILIACS TREATED WITH LOW-PURITY FACTOR-VIII. LANCET, 342(8869), 462-464.

LANGERHANS CELL HISTIOCYTOSIS PRESENTING WITH THE SUPERIOR VENA-CAVA SYNDROME - A CASE-REPORT
Mogul, M., HARTMAN, G., Donaldson, S., Gelb, A., Link, M., & Glader, B. (1993). LANGERHANS CELL HISTIOCYTOSIS PRESENTING WITH THE SUPERIOR VENA-CAVA SYNDROME - A CASE-REPORT. MEDICAL AND PEDIATRIC ONCOLOGY, 21(6), 456-459.

Arthropathy of the ankle in hemophilia.
Gamble, J. G., BELLAH, J., Rinsky, L. A., & Glader, B. (1991). Arthropathy of the ankle in hemophilia. journal of bone and joint surgery. American volume, 73(7), 1008-1015.

CRYPTOCOCCUS INFECTION IN A 9-YEAR-OLD CHILD WITH HEMOPHILIA AND THE ACQUIRED-IMMUNODEFICIENCY-SYNDROME
Ting, S. F., Glader, B. E., & Prober, C. G. (1991). CRYPTOCOCCUS INFECTION IN A 9-YEAR-OLD CHILD WITH HEMOPHILIA AND THE ACQUIRED-IMMUNODEFICIENCY-SYNDROME. PEDIATRIC INFECTIOUS DISEASE JOURNAL, 10(1), 76-77.

TREATMENT OF NEUTROPENIA ASSOCIATED WITH DYSKERATOSIS CONGENITA WITH GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR
Russo, C. L., Glader, B. E., Israel, R. J., & Galasso, F. (1990). TREATMENT OF NEUTROPENIA ASSOCIATED WITH DYSKERATOSIS CONGENITA WITH GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR. LANCET, 336(8717), 751-752.

RED-BLOOD-CELL APLASIAS IN CHILDREN
Glader, B. E. (1990). RED-BLOOD-CELL APLASIAS IN CHILDREN. PEDIATRIC ANNALS, 19(3), 168-?.

CONGENITAL HYPOPLASTIC (DIAMOND-BLACKFAN) ANEMIA IN 7 MEMBERS OF ONE KINDRED
Viskochil, D. H., Carey, J. C., Glader, B. E., Rothstein, G., & Christensen, R. D. (1990). CONGENITAL HYPOPLASTIC (DIAMOND-BLACKFAN) ANEMIA IN 7 MEMBERS OF ONE KINDRED. AMERICAN JOURNAL OF MEDICAL GENETICS, 35(2), 251-256.

SUP-HD1 - A NEW HODGKINS DISEASE-DERIVED CELL-LINE WITH LYMPHOID FEATURES PRODUCES INTERFERON-GAMMA
Naumovski, L., Utz, P. J., Bergstrom, S. K., Morgan, R., Molina, A., & Smith, S. D. (1989). SUP-HD1 - A NEW HODGKINS DISEASE-DERIVED CELL-LINE WITH LYMPHOID FEATURES PRODUCES INTERFERON-GAMMA. BLOOD, 74(8), 2733-2742.

REDUCED NEUTROPHIL COUNTS IN CHILDREN WITH TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD
Rogers, Z. R., Bergstrom, S. K., Amylon, M. D., Buchanan, G. R., & Glader, B. E. (1989). REDUCED NEUTROPHIL COUNTS IN CHILDREN WITH TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD. JOURNAL OF PEDIATRICS, 115(5), 746-748.

FAMILIAL BONE-MARROW MONOSOMY-7 - EVIDENCE THAT THE PREDISPOSING LOCUS IS NOT ON THE LONG ARM OF CHROMOSOME-7
Shannon, K. M., Turhan, A. G., Chang, S. Sy., Bowcock, A. M., Rogers, P. Cj., & Kan, Y. W. (1989). FAMILIAL BONE-MARROW MONOSOMY-7 - EVIDENCE THAT THE PREDISPOSING LOCUS IS NOT ON THE LONG ARM OF CHROMOSOME-7. JOURNAL OF CLINICAL INVESTIGATION, 84(3), 984-989.

HEMOGLOBIN FM-FORT-RIPLEY - ANOTHER LESSON FROM THE NEONATE
Glader, B. E. (1989). HEMOGLOBIN FM-FORT-RIPLEY - ANOTHER LESSON FROM THE NEONATE. PEDIATRICS, 83(5), 792-793.

HB F-M-OSAKA OR ALPHA-2G-GAMMA-263(E7)HIS-]TYR IN A CAUCASIAN MALE INFANT
Glader, B. E., ZWERDLING, D., Kutlar, F., Kutlar, A., Wilson, J. B., & Huisman, T. Hj. (1989). HB F-M-OSAKA OR ALPHA-2G-GAMMA-263(E7)HIS-]TYR IN A CAUCASIAN MALE INFANT. HEMOGLOBIN, 13(7-8), 769-773.

TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD
Glader, B. E. (1988). TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD. WESTERN JOURNAL OF MEDICINE, 149(4), 453-454.

PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC-LEUKEMIA CELL-LINES WITHOUT CLASSICAL BREAKPOINT CLUSTER REGION REARRANGEMENT
Naumovski, L., Morgan, R., Hecht, F., Link, M. P., Glader, B. E., & Smith, S. D. (1988). PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC-LEUKEMIA CELL-LINES WITHOUT CLASSICAL BREAKPOINT CLUSTER REGION REARRANGEMENT. CANCER RESEARCH, 48(10), 2876-2879.

CLINICAL AND BIOLOGIC CHARACTERIZATION OF T-CELL NEOPLASIAS WITH REARRANGEMENTS OF CHROMOSOME-7 BAND Q34
Smith, S. D., Morgan, R., Gemmell, R., Amylon, M. D., Link, M. P., & Hecht, F. (1988). CLINICAL AND BIOLOGIC CHARACTERIZATION OF T-CELL NEOPLASIAS WITH REARRANGEMENTS OF CHROMOSOME-7 BAND Q34. BLOOD, 71(2), 395-402.

ELEVATED RED-CELL ADENOSINE-DEAMINASE ACTIVITY - A MARKER OF DISORDERED ERYTHROPOIESIS IN DIAMOND-BLACKFAN ANEMIA AND OTHER HEMATOLOGIC DISEASES
Glader, B. E., & BACKER, K. (1988). ELEVATED RED-CELL ADENOSINE-DEAMINASE ACTIVITY - A MARKER OF DISORDERED ERYTHROPOIESIS IN DIAMOND-BLACKFAN ANEMIA AND OTHER HEMATOLOGIC DISEASES. BRITISH JOURNAL OF HAEMATOLOGY, 68(2), 165-168.

Diagnosis and management of red cell aplasia in children.
Glader, B. E. (1987). Diagnosis and management of red cell aplasia in children. Hematology/oncology clinics of North America, 1(3), 431-447.

ESTABLISHMENT AND CHARACTERIZATION OF A COMMON ACUTE LYMPHOBLASTIC-LEUKEMIA CELL-LINE WITH A DELETION OF CHROMOSOME-3 BAND Q26
Smith, S. D., Morgan, R., Galili, N., Amylon, M. D., Link, M. P., & Glader, B. E. (1987). ESTABLISHMENT AND CHARACTERIZATION OF A COMMON ACUTE LYMPHOBLASTIC-LEUKEMIA CELL-LINE WITH A DELETION OF CHROMOSOME-3 BAND Q26. CANCER RESEARCH, 47(6), 1652-1656.

TRANSIENT ERYTHROBLASTOPENIA OF ADOLESCENCE
Zwerdling, T., Finlay, J., & Glader, B. E. (1986). TRANSIENT ERYTHROBLASTOPENIA OF ADOLESCENCE. CLINICAL PEDIATRICS, 25(11), 563-565.

PYRUVATE-KINASE DEFICIENCY IN DOG AND HUMAN-ERYTHROCYTES - EFFECTS OF ENERGY DEPLETION ON CATION COMPOSITION AND CELLULAR HYDRATION
MULLERSOYANO, A., Platt, O., & Glader, B. E. (1986). PYRUVATE-KINASE DEFICIENCY IN DOG AND HUMAN-ERYTHROCYTES - EFFECTS OF ENERGY DEPLETION ON CATION COMPOSITION AND CELLULAR HYDRATION. AMERICAN JOURNAL OF HEMATOLOGY, 23(3), 217-221.

PREDNISONE STIMULATION OF ERYTHROPOIESIS IN LEUKEMIC CHILDREN DURING REMISSION
Amylon, M. D., Perrine, S. P., & Glader, B. E. (1986). PREDNISONE STIMULATION OF ERYTHROPOIESIS IN LEUKEMIC CHILDREN DURING REMISSION. AMERICAN JOURNAL OF HEMATOLOGY, 23(2), 179-181.

COMPARATIVE ACTIVITY OF ERYTHROCYTE ADENOSINE-DEAMINASE AND OROTIDINE DECARBOXYLASE IN DIAMOND-BLACKFAN ANEMIA
Glader, B. E., & BACKER, K. (1986). COMPARATIVE ACTIVITY OF ERYTHROCYTE ADENOSINE-DEAMINASE AND OROTIDINE DECARBOXYLASE IN DIAMOND-BLACKFAN ANEMIA. AMERICAN JOURNAL OF HEMATOLOGY, 23(2), 135-139.

SCREENING FOR ANEMIA AND ERYTHROCYTE DISORDERS IN CHILDREN
Glader, B. E. (1986). SCREENING FOR ANEMIA AND ERYTHROCYTE DISORDERS IN CHILDREN. PEDIATRICS, 78(2), 368-369.

CHRONIC INFECTIOUS-MONONUCLEOSIS SYNDROME, PANCYTOPENIA, AND POLYCLONAL B-LYMPHOPROLIFERATION TERMINATING IN ACUTE LYMPHOBLASTIC-LEUKEMIA
Finlay, J., Luft, B., Yousem, S., Wood, G. S., Link, M., & PURTILO, D. (1986). CHRONIC INFECTIOUS-MONONUCLEOSIS SYNDROME, PANCYTOPENIA, AND POLYCLONAL B-LYMPHOPROLIFERATION TERMINATING IN ACUTE LYMPHOBLASTIC-LEUKEMIA. AMERICAN JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 8(1), 18-27.

PANCYTOPENIA WITH MYELOFIBROSIS - AN UNUSUAL PRESENTATION OF CHILDHOOD HODGKINS-DISEASE
Carroll, W. L., Berberich, F. R., & Glader, B. E. (1986). PANCYTOPENIA WITH MYELOFIBROSIS - AN UNUSUAL PRESENTATION OF CHILDHOOD HODGKINS-DISEASE. CLINICAL PEDIATRICS, 25(2), 106-108.

MONO-VALENT CATION CHANGES IN SICKLE ERYTHROCYTES - A DIRECT REFLECTION OF ALPHA-GLOBIN GENE NUMBER
Embury, S. H., BACKER, K., & Glader, B. E. (1985). MONO-VALENT CATION CHANGES IN SICKLE ERYTHROCYTES - A DIRECT REFLECTION OF ALPHA-GLOBIN GENE NUMBER. JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 106(1), 75-79.

CHILDHOOD BONE-MARROW MONOSOMY-7 SYNDROME - A FAMILIAL DISORDER
Carroll, W. L., Morgan, R., & Glader, B. E. (1985). CHILDHOOD BONE-MARROW MONOSOMY-7 SYNDROME - A FAMILIAL DISORDER. JOURNAL OF PEDIATRICS, 107(4), 578-580.

FATAL MYOCARDIAL-INFARCTION FOLLOWING THERAPY WITH PROTHROMBIN COMPLEX CONCENTRATES IN A YOUNG MAN WITH HEMOPHILIA-A
Sullivan, D. W., Purdy, L. J., Billingham, M., & Glader, B. E. (1984). FATAL MYOCARDIAL-INFARCTION FOLLOWING THERAPY WITH PROTHROMBIN COMPLEX CONCENTRATES IN A YOUNG MAN WITH HEMOPHILIA-A. PEDIATRICS, 74(2), 279-281.

IMMUNE THROMBOCYTOPENIA ASSOCIATED WITH ACUTE NONLYMPHOCYTIC LEUKEMIA
Amylon, M. D., Link, M. P., & Glader, B. E. (1984). IMMUNE THROMBOCYTOPENIA ASSOCIATED WITH ACUTE NONLYMPHOCYTIC LEUKEMIA. JOURNAL OF PEDIATRICS, 105(5), 776-778.

MONOCLONAL-ANTIBODY AND ENZYMATIC PROFILES OF HUMAN-MALIGNANT LYMPHOID-T CELLS AND DERIVED CELL-LINES
Smith, S. D., Shatsky, M., Cohen, P. S., Warnke, R., Link, M. P., & Glader, B. E. (1984). MONOCLONAL-ANTIBODY AND ENZYMATIC PROFILES OF HUMAN-MALIGNANT LYMPHOID-T CELLS AND DERIVED CELL-LINES. CANCER RESEARCH, 44(12), 5657-5660.

ACUTE NONLYMPHOCYTIC LEUKEMIA DEVELOPING DURING THE COURSE OF EWINGS-SARCOMA
Link, M. P., Donaldson, S. S., Kempson, R. L., Wilbur, J. R., & Glader, B. E. (1984). ACUTE NONLYMPHOCYTIC LEUKEMIA DEVELOPING DURING THE COURSE OF EWINGS-SARCOMA. MEDICAL AND PEDIATRIC ONCOLOGY, 12(3), 194-200.

COMPARATIVE MONO-VALENT CATION-TRANSPORT IN NEONATAL AND ADULT RED-BLOOD-CELLS
MULLERSOYANO, A., Ramsey, B. W., & Glader, B. E. (1984). COMPARATIVE MONO-VALENT CATION-TRANSPORT IN NEONATAL AND ADULT RED-BLOOD-CELLS. PEDIATRIC RESEARCH, 18(8), 778-780.

ELEVATED ERYTHROCYTE ADENOSINE-DEAMINASE ACTIVITY IN CONGENITAL HYPOPLASTIC-ANEMIA
Glader, B. E., BACKER, K., & DIAMOND, L. K. (1983). ELEVATED ERYTHROCYTE ADENOSINE-DEAMINASE ACTIVITY IN CONGENITAL HYPOPLASTIC-ANEMIA. NEW ENGLAND JOURNAL OF MEDICINE, 309(24), 1486-1490.

PLATELET-ASSOCIATED IMMUNOGLOBULIN-G IN CHILDHOOD IDIOPATHIC THROMBOCYTOPENIC PURPURA
Cheung, N. Kv., Hilgartner, M. W., Schulman, I., McFall, P., & Glader, B. E. (1983). PLATELET-ASSOCIATED IMMUNOGLOBULIN-G IN CHILDHOOD IDIOPATHIC THROMBOCYTOPENIC PURPURA. JOURNAL OF PEDIATRICS, 102(3), 366-370.

THE RED-BLOOD-CELL AS A BIOPSY TOOL
Glader, B. E., & Sullivan, D. W. (1981). THE RED-BLOOD-CELL AS A BIOPSY TOOL. CLINICS IN HAEMATOLOGY, 10(1), 209-222.

ERYTHROCYTE ENZYME DISORDERS IN CHILDREN
Sullivan, D. W., & Glader, B. E. (1980). ERYTHROCYTE ENZYME DISORDERS IN CHILDREN. PEDIATRIC CLINICS OF NORTH AMERICA, 27(2), 449-462.

HEREDITARY SPHEROCYTOSIS
Sullivan, D. W., & Glader, B. E. (1980). HEREDITARY SPHEROCYTOSIS. PEDIATRIC ANNALS, 9(8), 308-311.

Erythrocyte disorders leading to potassium loss and cellular dehydration.
Glader, B. E., & Sullivan, D. W. (1979). Erythrocyte disorders leading to potassium loss and cellular dehydration. Progress in clinical and biological research, 30, 503-513.

MICROCYTOSIS ASSOCIATED WITH SICKLE-CELL ANEMIA
Glader, B. E., PROPPER, R. D., & Buchanan, G. R. (1979). MICROCYTOSIS ASSOCIATED WITH SICKLE-CELL ANEMIA. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 72(1), 63-64.

EOSINOPHILIA IN CHILDREN
Foung, S., & Glader, B. E. (1979). EOSINOPHILIA IN CHILDREN. PEDIATRIC ANNALS, 8(6), 39-?.

LEUKOCYTE COUNTS IN CHILDREN WITH SICKLE-CELL DISEASE - COMPARATIVE VALUES IN STEADY-STATE, VASO-OCCLUSIVE CRISIS, AND BACTERIAL-INFECTION
Buchanan, G. R., & Glader, B. E. (1978). LEUKOCYTE COUNTS IN CHILDREN WITH SICKLE-CELL DISEASE - COMPARATIVE VALUES IN STEADY-STATE, VASO-OCCLUSIVE CRISIS, AND BACTERIAL-INFECTION. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 132(4), 396-398.

RED-BLOOD-CELL SIZE AND GLYCOLYTIC ENZYME-ACTIVITY - RELATIONSHIP TO NUMBER OF INTRA-MEDULLARY CELL DIVISIONS
Glader, B. E., McCrimmons, D., MULLERSOYANO, A., & Platt, O. (1978). RED-BLOOD-CELL SIZE AND GLYCOLYTIC ENZYME-ACTIVITY - RELATIONSHIP TO NUMBER OF INTRA-MEDULLARY CELL DIVISIONS. PEDIATRIC RESEARCH, 12(4), 308-309.

ENERGY RESERVE AND CATION COMPOSITION OF IRREVERSIBLY SICKLED CELLS INVIVO
Glader, B. E., Lux, S. E., MULLERSOYANO, A., Platt, O. S., PROPPER, R. D., & Nathan, D. G. (1978). ENERGY RESERVE AND CATION COMPOSITION OF IRREVERSIBLY SICKLED CELLS INVIVO. BRITISH JOURNAL OF HAEMATOLOGY, 40(4), 527-532.

CATION PERMEABILITY ALTERATIONS DURING SICKLING - RELATIONSHIP TO CATION COMPOSITION AND CELLULAR HYDRATION OF IRREVERSIBLY SICKLED CELLS
Glader, B. E., & Nathan, D. G. (1978). CATION PERMEABILITY ALTERATIONS DURING SICKLING - RELATIONSHIP TO CATION COMPOSITION AND CELLULAR HYDRATION OF IRREVERSIBLY SICKLED CELLS. BLOOD, 51(5), 983-989.

HEMOLYTIC DISORDERS OF INFANCY
Glader, B. E., & Platt, O. (1978). HEMOLYTIC DISORDERS OF INFANCY. CLINICS IN HAEMATOLOGY, 7(1), 35-61.

PHYSIOLOGIC FEATURES OF HEMOLYSIS ASSOCIATED WITH ALTERED CATION AND 2,3-DIPHOSPHOGLYCERATE CONTENT
ALBALA, M. M., FORTIER, N. L., & Glader, B. E. (1978). PHYSIOLOGIC FEATURES OF HEMOLYSIS ASSOCIATED WITH ALTERED CATION AND 2,3-DIPHOSPHOGLYCERATE CONTENT. BLOOD, 52(1), 135-141.

CATION SPECIFICITY OF PROPRANOLOL-INDUCED CHANGES IN RBC MEMBRANE-PERMEABILITY - COMPARATIVE EFFECTS IN HUMAN, DOG AND CAT ERYTHROCYTES
MULLERSOYANO, A., & Glader, B. E. (1977). CATION SPECIFICITY OF PROPRANOLOL-INDUCED CHANGES IN RBC MEMBRANE-PERMEABILITY - COMPARATIVE EFFECTS IN HUMAN, DOG AND CAT ERYTHROCYTES. JOURNAL OF CELLULAR PHYSIOLOGY, 91(2), 317-321.

BENIGN COURSE OF EXTREME HYPERBILIRUBINEMIA IN SICKLE-CELL ANEMIA - ANALYSIS OF 6 CASES
Buchanan, G. R., & Glader, B. E. (1977). BENIGN COURSE OF EXTREME HYPERBILIRUBINEMIA IN SICKLE-CELL ANEMIA - ANALYSIS OF 6 CASES. JOURNAL OF PEDIATRICS, 91(1), 21-24.

Care of the critically ill child: the bleeding neonate.
Glader, B. E., & Buchanan, G. R. (1976). Care of the critically ill child: the bleeding neonate. Pediatrics, 58(4), 548-555.

EVALUATION OF HEMOLYTIC ROLE OF ASPIRIN IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY
Glader, B. E. (1976). EVALUATION OF HEMOLYTIC ROLE OF ASPIRIN IN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY. JOURNAL OF PEDIATRICS, 89(6), 1027-1028.

SALICYLATE-INDUCED INJURY OF PYRUVATE-KINASE-DEFICIENT ERYTHROCYTES
Glader, B. E. (1976). SALICYLATE-INDUCED INJURY OF PYRUVATE-KINASE-DEFICIENT ERYTHROCYTES. NEW ENGLAND JOURNAL OF MEDICINE, 294(17), 916-918.

ENERGY METABOLISM IN HUMAN ERYTHROCYTES - ROLE OF PHOSPHOGLYCERATE KINASE IN CATION-TRANSPORT
Segel, G. B., Feig, S. A., Glader, B. E., Muller, A., Dutcher, P., & Nathan, D. G. (1975). ENERGY METABOLISM IN HUMAN ERYTHROCYTES - ROLE OF PHOSPHOGLYCERATE KINASE IN CATION-TRANSPORT. BLOOD, 46(2), 271-278.

INVIVO HEPATIC AND INTESTINAL TOXICITY OF SODIUM CYANATE IN RATS - CYANATE-INDUCED ALTERATIONS IN HEPATIC GLYCOGEN-METABOLISM
Haut, M. J., Toskes, P. P., Hildebrandt, P. K., Glader, B. E., & Conrad, M. E. (1975). INVIVO HEPATIC AND INTESTINAL TOXICITY OF SODIUM CYANATE IN RATS - CYANATE-INDUCED ALTERATIONS IN HEPATIC GLYCOGEN-METABOLISM. JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 85(1), 140-154.

ROLE OF ELEVATED GLUCOSE CONCENTRATIONS IN HEMOLYSIS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENT ERYTHROCYTES
Glader, B. E. (1975). ROLE OF ELEVATED GLUCOSE CONCENTRATIONS IN HEMOLYSIS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENT ERYTHROCYTES. PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 148(1), 50-53.

HEMOLYSIS DUE TO PYRUVATE-KINASE DEFICIENCY AND OTHER GLYCOLYTIC ENZYMOPATHIES
Glader, B. E., & Nathan, D. G. (1975). HEMOLYSIS DUE TO PYRUVATE-KINASE DEFICIENCY AND OTHER GLYCOLYTIC ENZYMOPATHIES. CLINICS IN HAEMATOLOGY, 4(1), 123-138.

CONGENITAL HEMOLYTIC-ANEMIA ASSOCIATED WITH DEHYDRATED ERYTHROCYTES AND INCREASED POTASSIUM LOSS
Glader, B. E., FORTIER, N., ALBALA, M. M., & Nathan, D. G. (1974). CONGENITAL HEMOLYTIC-ANEMIA ASSOCIATED WITH DEHYDRATED ERYTHROCYTES AND INCREASED POTASSIUM LOSS. NEW ENGLAND JOURNAL OF MEDICINE, 291(10), 491-496.

ONCORNA VIRUS DISEASE - SYNDROME OF HEMOLYTIC-ANEMIA AND LYMPH-NODE CYSTIC-DISEASE
Siegler, R., Moran, S., Glader, B., Lane, I., & FROSCH, Y. (1974). ONCORNA VIRUS DISEASE - SYNDROME OF HEMOLYTIC-ANEMIA AND LYMPH-NODE CYSTIC-DISEASE. LABORATORY INVESTIGATION, 30(5), 626-638.

EFFECT OF CYANATE ON ERYTHROCYTE DEFORMABILITY
DUROCHER, J. R., Glader, B. E., GAINES, L. T., & Conrad, M. E. (1974). EFFECT OF CYANATE ON ERYTHROCYTE DEFORMABILITY. BLOOD, 43(2), 277-280.

CONGENITAL HEMOLYTIC-ANEMIA WITH POTASSIUM LOSS - REPLY
Glader, B. E., Nathan, D. G., ALBALA, M. M., & FORTIER, N. (1974). CONGENITAL HEMOLYTIC-ANEMIA WITH POTASSIUM LOSS - REPLY. NEW ENGLAND JOURNAL OF MEDICINE, 291(25), 1361-1361.

EFFECT OF CYANATE ON ERYTHROCYTE-MEMBRANE SURFACE CHARGE
DUROCHER, J. R., Glader, B. E., & Conrad, M. E. (1973). EFFECT OF CYANATE ON ERYTHROCYTE-MEMBRANE SURFACE CHARGE. PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 144(1), 249-251.

INTRAVASCULAR HEMOLYSIS ASSOCIATED WITH INTRAVENOUS UREA INFUSIONS IN NORMAL INDIVIDUALS
BENSINGE, T. A., Glader, B. E., & Conrad, M. E. (1973). INTRAVASCULAR HEMOLYSIS ASSOCIATED WITH INTRAVENOUS UREA INFUSIONS IN NORMAL INDIVIDUALS. BLOOD, 41(3), 461-464.

HEMOLYSIS BY DIPHENYLSULFONES - COMPARATIVE EFFECTS OF DDS AND HYDROXYLAMINE-DDS
Glader, B. E., & Conrad, M. E. (1973). HEMOLYSIS BY DIPHENYLSULFONES - COMPARATIVE EFFECTS OF DDS AND HYDROXYLAMINE-DDS. JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 81(2), 267-272.

DECREASED GLUTATHIONE PEROXIDASE IN NEONATAL ERTHYROCYTES - LACK OF RELATION TO HYDROGEN-PEROXIDE METABOLISM
Glader, B. E., & Conrad, M. E. (1972). DECREASED GLUTATHIONE PEROXIDASE IN NEONATAL ERTHYROCYTES - LACK OF RELATION TO HYDROGEN-PEROXIDE METABOLISM. PEDIATRIC RESEARCH, 6(12), 900-904.

CYANATE INHIBITION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE
Glader, B. E., & Conrad, M. E. (1972). CYANATE INHIBITION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE. NATURE, 237(5354), 336-?.

MECHANISM OF METHEMOGLOBIN FORMATION BY DIPHENYLSULFONES - EFFECT OF 4-AMINO-4'-HYDROXYAMINODIPHENYLSULFONE AND OTHER P-SUBSTITUTED DERIVATIVES
Kramer, P. A., LI, T. K., & Glader, B. E. (1972). MECHANISM OF METHEMOGLOBIN FORMATION BY DIPHENYLSULFONES - EFFECT OF 4-AMINO-4'-HYDROXYAMINODIPHENYLSULFONE AND OTHER P-SUBSTITUTED DERIVATIVES. BIOCHEMICAL PHARMACOLOGY, 21(9), 1265-?.

EFFECT OF COBALT UPON IRON ABSORPTION
Schade, S. G., FELSHER, B. F., Glader, B. E., & Conrad, M. E. (1970). EFFECT OF COBALT UPON IRON ABSORPTION. PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE, 134(3), 741-?.

Observations on the effect of testosterone and hydrocortisone on erythropoiesis.
Glader, B. E., RAMBACH, W. A., & ALT, H. L. (1968). Observations on the effect of testosterone and hydrocortisone on erythropoiesis. Annals of the New York Academy of Sciences, 149(1), 383-388.

OBSERVATIONS ON EFFECT OF TESTOSTERONE AND HYDROCORTISONE ON ERYTHROPOIESIS
Glader, B. E., RAMBACH, W. A., & ALT, H. L. (1968). OBSERVATIONS ON EFFECT OF TESTOSTERONE AND HYDROCORTISONE ON ERYTHROPOIESIS. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 149(A1), 383-?.

ROLE OF CELLULAR PI IN PI TRANSPORT AND METABOLISM IN HUMAN RED CELLS
Glader, B. E., & Omachi, A. (1968). ROLE OF CELLULAR PI IN PI TRANSPORT AND METABOLISM IN HUMAN RED CELLS. BIOCHIMICA ET BIOPHYSICA ACTA, 150(3), 524-?.

PHOSPHATE RELEASE FROM HUMAN ERYTHROCYTES
Glader, B. E., & Omachi, A. (1968). PHOSPHATE RELEASE FROM HUMAN ERYTHROCYTES. BIOCHIMICA ET BIOPHYSICA ACTA, 163(1), 30-?.

2,4-DINITROPHENOL INHIBITION OF P32 RELEASE FROM HUMAN RED CELLS
Omachi, A., Scott, C. B., & Glader, B. E. (1968). 2,4-DINITROPHENOL INHIBITION OF P32 RELEASE FROM HUMAN RED CELLS. EXPERIENTIA, 24(3), 244-?.