Search Results - "ZINKHAM, W. H"

Henna : A potential cause of oxidative hemolysis and neonatal hyperbilirubinemia by ZINKHAM, W. H, OSKI, F. A

“…To evaluate the in vitro oxidation potential of lawsone (2-hydroxy-1,4 naphthoquinone). Lawsone is a chemical present in henna, the crushed leaves of which are…”
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Kasabach-Merritt syndrome: therapeutic considerations by LARSEN, E. C, ZINKHAM, W. H, EGGLESTON, J. C, ZITELLI, B. J

“…During the past 15 years we have managed six children with capillary hemangiomas in association with consumptive coagulopathy--the Kasabach-Merritt syndrome…”
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Partial deficiency of erythrocyte spectrin in hereditary spherocytosis by Agre, Peter, Casella, James F, Zinkham, William H, McMillan, Campbell, Bennett, Vann

“…Hereditary spherocytosis (HS) is a common, clinically heterogeneous haemolytic anaemia in which the primary erythrocyte defect is believed to be some…”
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Twenty-nail dystrophy associated with hematologic abnormalities by Germain-Lee, E L, Zinkham, W H

“…This report describes a 15 1/2 year old white male with twenty-nail dystrophy who has had recurrent episodes of immune thrombocytopenic purpura, autoimmune…”
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Variable degrees of suppression of hemoglobin S synthesis in subjects with hemoglobin SS disease on a long-term transfusion regimen by Zinkham, William H., Seidler, Alexander J., Kickler, Thomas S.

“…The objectives of this study were to quantify the amount of blood required to suppress synthesis of hemoglobin S (HbS) in patients with hemoglobin SS on a…”
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Homozygous protein C deficiency: observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy by PETERS, C, CASELLA, J. F, MARLAR, R. A, MONTGOMERY, R. R, ZINKHAM, W. H

“…An infant with severe homozygous protein C deficiency was brought to medical attention because of purpura fulminans and severe bilateral vitreous hemorrhages…”
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Hb Catonsville (glutamic acid inserted between Pro-37(C2)alpha and Thr-38(C3)alpha). Nonallelic gene conversion in the globin system? by Moo-Penn, W F, Swan, D C, Hine, T K, Baine, R M, Jue, D L, Benson, J M, Johnson, M H, Virshup, D M, Zinkham, W H

“…Hb Catonsville is an unstable variant in which glutamic acid is inserted into the alpha-globin chain between Pro-37(C2) and Thr-38(C3). The peptide sequence…”
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Linkage of Lactate Dehydrogenase B and C Loci in Pigeons by Zinkham, W. H., Isensee, H.

“…Synthesis of lactate dehydrogenase in somatic and gametic tissues of certain avian and mammalian species is controlled by alleles at three loci, A, B, and C…”
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Gonadal function in two siblings with Fanconi's anemia by Berkovitz, G D, Zinkham, W H, Migeon, C J

“…2 siblings with Fanconi's anemia, 1 male and 1 female, aged 22 and 24 years, respectively, were evaluated at the Johns Hopkins Hospital because of short…”
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Phenotypic variability in siblings with Farber disease by Antonarakis, S E, Valle, D, Moser, H W, Moser, A, Qualman, S J, Zinkham, W H

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Methylene blue-induced Heinz body hemolytic anemia by Sills, M R, Zinkham, W H

“…To describe the manifestations of methylene blue toxicity, with a review of the literature. A descriptive analysis of physical findings and significant…”
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Carboxyhemoglobin Levels in an Unstable Hemoglobin Disorder (Hb Zürich): Effect on Phenotypic Expression by Zinkham, W. H., Houtchens, R. A., Caughey, W. S.

“…The affinity of Hb Zürich for carbon monoxide is approximately 65 times that of normal hemoglobin. The carboxyhemoglobin content in serum from individuals with…”
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Peripheral blood and bilirubin values in normal full-term primaquine-sensitive Negro infants: effect of vitamin K by ZINKHAM, W H

“…Serial determinations of hematocrit, reticulocyte, and bilirubin values were carried out during the first 8 days of life in 30 fullterm primaquine-sensitive…”
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Hemoglobin SC, SS/GPhiladelphia and SOArab diseases diagnostic importance of an integrative analysis of clinical, hematologic and electrophoretic findings by Charache, S, Zinkham, W H, Dickerman, J D, Brimhall, B, Dover, G J

“…Hemoglobin studies are presented on two children in whom electrophoretic analysis of hemolysates at alkaline pH initially suggested the diagnosis of hemoglobin…”
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A defect of glutathione metabolism in erythrocytes from patients with a naphthalene-induced hemolytic anemia by ZINKHAM, W H, CHILDS, B

“…Four patients are reported who suffered hemobytic anemia after exposure to naphthalene. These were all Negroes; three were male and one female. All the…”
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Visceral larva migrans due to Toxocara as a cause of eosinophilia by Zinkham, W H

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Polymorphism of Lactate Dehydrogenase Isozymes in Pigeons by ZINKHAM, WM. H, KUPCHYK, L, BLANCO, A, ISENSEE, H

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Farber disease: pathologic diagnosis in sibs with phenotypic variability by Qualman, S J, Moser, H W, Valle, D, Moser, A E, Antonarakis, S E, Boitnott, J K, Zinkham, W H

“…We describe new pathologic findings in two sibs with Farber lipogranulomatosis. The first child, a 3-month-old boy, presented with only hepatosplenomegaly and…”
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Isozymes: biological and clinical significance by Zinkham, W H, Blanco, A, Kupchyk, L

“…A RECENT and rather surprising discovery in biochemistry was the finding that a single enzyme can exist in several different forms within a single tissue. This…”
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Varicella-associated thrombocytopenia: clues to the etiology of childhood idiopathic thrombocytopenic purpura by Yeager, A M, Zinkham, W H

“…The temporal patterns of varicella-associated thrombocytopenia in five children seen at the Johns Hopkins Hospital suggest the existence of at least two…”
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