Search Results - "Broxson, E H"
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Treatment of diencephalic syndrome with chemotherapy: Growth, tumor response, and long term control
Published in Cancer (01-07-1998)“…The diencephalic syndrome (DS), which is manifested by progressive emaciation and failure to thrive in an apparently alert, cheerful infant, usually is due to…”
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Prevalence of von Willebrand disease in children: a multiethnic study
Published in The Journal of pediatrics (01-12-1993)“…Von Willebrand disease (vWD) was thought to be a rare disorder until a recent survey reported a prevalence of 0.8% in an ethnically homogenous community in…”
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A 5.3-kb Deletion Including Exon XIII of the Protein S α Gene Occurs in Two Protein S-Deficient Families
Published in Blood (01-02-1991)“…Genomic DNA samples from 12 protein S-deficient families with hereditary thrombophilia were analyzed by Southern hybridization using protein S cDNA probes…”
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Normal vitamin E status in sickle hemoglobinopathies in Colorado
Published in The American journal of clinical nutrition (01-09-1989)“…Because previous studies of serum or plasma vitamin E (E) levels reported a high prevalence of E deficiency in patients with sickle cell anemia (SCA), we…”
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Changes in plasma methionine and total homocysteine levels in patients receiving methotrexate infusions
Published in Cancer research (Chicago, Ill.) (01-11-1989)“…Methotrexate reduces intracellular pools of 5-methyltetrahydrofolate and could result in reduced conversion of homocysteine to methionine by methionine…”
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Transplacental transfer of acquired factor VIII: C inhibitor
Published in Thrombosis and haemostasis (03-02-1987)Get more information
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Hb Muskegon [beta 83(EF7)Gly-->Arg]: a new variant found in a family from the U.S
Published in Hemoglobin (1993)Get more information
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The erythropoietin receptor gene is not linked with the polycythemia phenotype in a family with autosomal dominant primary polycythemia
Published in Proceedings of the Association of American Physicians (01-11-1997)“…Primary familial and congenital polycythemia (PFCP or familial erythrocytosis) is a rare hematological disorder with either autosomal-dominant inheritance or…”
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Relative value of diagnostic studies for von Willebrand disease
Published in The Journal of pediatrics (01-07-1992)“…Laboratory tests recommended to screen patients with mucosal bleeding for hemostatic disorders generally include determinations of prothrombin time, partial…”
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Portal hypertension develops in a subset of children with standard risk acute lymphoblastic leukemia treated with oral 6-thioguanine during maintenance therapy
Published in Pediatric Blood & Cancer (01-03-2005)“…Background 6‐Thioguanine (TG) was recently studied to determine whether TG in maintenance therapy achieves better event free survival than 6‐mercaptopurine…”
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606 Utility of screening for iron deficiency anemia in pediatric patients
Published in Journal of pediatric hematology/oncology (01-11-1996)Get full text
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Epstein-Barr virus-associated lymphoma in a child undergoing an autologous stem cell rescue
Published in Journal of pediatric hematology/oncology (01-02-2002)“…Epstein-Barr virus-associated lymphoproliferative disease (EBV-LPD) is a serious disorder seen in various states of immunodeficiency, often with a fatal…”
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A 5.3-kb deletion including exon XIII of the protein S alpha gene occurs in two protein S-deficient families [see comments]
Published in Blood (01-02-1991)“…Genomic DNA samples from 12 protein S-deficient families with hereditary thrombophilia were analyzed by Southern hybridization using protein S cDNA probes…”
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