Search Results - "Vida, L N"

Juvenile myelomonocytic leukemia (JMML) with the hematologic phenotype of severe β thalassemia by Honig, George R., Suarez, Carlos R., Vida, Loyda N., Lu, Shi‐Jiang, Liu, Edison T.

“…A 3‐year‐old Filipino‐American child with recurrent fever, splenomegaly, anemia, and thrombocytopenia, was found to have a hemoglobin F level of 76.9%. His…”
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Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease by NORONHA, P. A, VIDA, L. N, PARK, C. L, HONIG, G. R

“…Human hemoglobins (Hbs) are known to be immunogenic, and both normal and variant forms of Hb have been shown to stimulate antibody formation in a variety of…”
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Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure by HONIG, G. R, VIDA, L. N, ROSENBLUM, B. B, PERUTZ, M. F, FERMI, G

“…In Hb Warsaw Val replaces the Phe normally present at the heme contact position beta 42 (CD1). This variant is unstable, and it readily undergoes methemoglobin…”
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Fetal hemoglobin expression in transplant recipients of placental blood hematopoietic progenitor cells by HONIG, G. R, VIDA, L. N, HOGANSON, G. E, SCHULTZ, J. C, SHAHIDI, N. T

“…Patients who achieved bone marrow engraftment of cord blood-derived progenitor cells provided an opportunity to examine the expression of fetal Hb by neonatal…”
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Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia by Honig, G R, Shamsuddin, M, Vida, L N, Mompoint, M, Valcourt, E, Bowie, L J, Jones, E C, Powers, P A, Spritz, R A, Guis, M

“…A new hematologic syndrome with phenotypic features of mild Hb H disease was identified in three children from two unrelated black American families…”
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Hemoglobin Lincoln Park: a betadelta fusion (anti-Lepore) variant with an amino acid deletion in the delta chain-derived segment by Honig, G R, Shamsuddin, M, Mason, R G, Vida, L N

“…An electrophoretically slow-moving hemoglobin variant was identified in three members of a family originating from Southern Mexico. The variant, Hb Lincoln…”
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Similarities of the Erythrocytes in Juvenile Chronic Myelogenous Leukemia to Fetal Erythrocytes by Maurer, Helen S., Vida, Loyda N., Honig, George R.

“…A 4-yr-old boy was studied who showed typical findings of juvenile chronic myelogenous leukemia, including massive hepatosplenomegaly, thrombocytopenia, low…”
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Two New Sickle Cell Syndromes: HbS, Hb Camden, and α-Thalassemia; and HbS in Combination With Hb Tacoma by Honig, George R, Mason, R. George, Shamsuddin, Mir, Vida, Loyda N, Rao, Koduri R.P, Patel, Ashok R

“…Hemoglobin variants having electrophoretic mobility more rapid than that of HbA were identified in combination with sickle hemoglobin in two patients at the…”
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Hb south Milwaukee [beta 105 (G7) Leu----Phe]: a newly-identified hemoglobin variant with high oxygen affinity by Honig, G R, Vida, L N, Latorraca, R, Divgi, A B

“…Fifteen individuals among four generations of a family of English ancestry demonstrated elevated hemoglobin levels accompanied by leftward-shifted whole blood…”
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Synthesis of Hemoglobin Abraham Lincoln (ß 32 leu →pro) by Honig, George R., Mason, R. George, Vida, Loyda N., Shamsuddin, Mir

“…Globin chain synthesis was studied in vitro with reticulocytes from a patient heterozygous for Hb Abraham Lincoln, an unstable beta chain variant. Synthesis of…”
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Hb Warsaw (beta 42 Phe----Val): an unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression by Honig, G R, Telfer, M C, Rosenblum, B B, Vida, L N

“…Four members in two generations of a Polish-American family exhibited findings of congenital Heinz-body hemolytic anemia accompanied by cyanosis. Two of the…”
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Hb Mizuho [beta 68(E12)Leu----Pro]. Second occurrence identified in a Caucasian child with hemolytic anemia and dense erythrocyte inclusions by Labotka, R J, Vida, L N, Honig, G R

“…Hb Mizuho [beta 68(E12)Leu---Pro] was identified in a child of Italian/Sicilian descent who exhibited severe, transfusion dependent hemolytic anemia which…”
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Modelling whole blood oxygen equilibrium: comparison of nine different models fitted to normal human data by O'Riordan, J F, Goldstick, T K, Vida, L N, Honig, G R, Ernest, J T

“…The ability of nine different models, prominent in the literature, to meaningfully characterize the oxygen-hemoglobin equilibrium curve (OHEC) of normal…”
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Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia by Honig, G R, Gunay, U, Mason, R G, Vida, L N, Ferenc, C

“…Hematologic and globin synthesis studies were performed in a black American family in which the genes for alpha-thalassemia and hemoglobins (Hb) S and C were…”
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Hemoglobin Korle Bu in a Mexican family by Honig, G R, Seeler, R A, Shamsuddin, M, Vida, L N, Mompoint, M, Valcourt, E

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Evaluation of Fagara zanthoxyloides root extract in sickle cell anemia blood in vitro by Honig, G R, Farnsworth, N R, Ferenc, C, Vida, L N

“…An aqueous extract was prepared from roots of Fagara zanthoxyloides and examined for evidence of an antisickling effect in vitro. Addition of 25 mg/ml of the…”
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Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia by Honig, G R, Shamsuddin, M, Mason, R G, Vida, L N, Tremaine, L M, Tarr, G E, Shahidi, N T

“…Hematologic evaluation of a Nigerian obstetrical patient disclosed the presence of sickle-cell trait as well as evidence of a hemoglobin alpha-chain…”
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Hemoglobin Nigeria (alpha-81 Ser replaced by Cys):a new variant associated with alpha-thalassemia by Honig, GR, Shamsuddin, M, Mason, RG, Vida, LN, Tremaine, LM, Tarr, GE, Shahidi, NT

“…Hematologic evaluation of a Nigerian obstetrical patient disclosed the presence of sickle-cell trait as well as evidence of a hemoglobin alpha- chain…”
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Globin chain synthesis in sickle cell trait under conditions of folate antagonism by Honig, G R, Mason, R G, Vida, L N

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Hemoglobin Warsaw (Phe super( beta 42(CD1)) arrow right Val), an unstable variant with decreased oxygen affinity. Characterization of its synthesis, functional properties, and structure by Honig, G R, Vida, L N, Rosenblum, B B, Perutz, M F, Fermi, G

“…In Hb Warsaw Val replaces the Phe normally present at the heme contact position beta 42 (CD1). This variant is unstable, and it readily undergoes methemoglobin…”
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