Search Results - "Vida, Loyda N"

Analyses of in vitro nonenzymatic glycation of normal and variant hemoglobins by MALDI-TOF mass spectrometry by Lee, Bao-Shiang, Jayathilaka, G D Lasanthi P, Huang, Jin-Sheng, Vida, Loyda N, Honig, George R, Gupta, Shalini

“…MALDI-TOF mass spectrometry is used here to differentiate different glycoisoforms of normal and variant hemoglobins (Hbs) in nonenzymatic in vitro glycation…”
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α-Thalassemia-Like Globin Gene Expression by Primitive Erythrocytes Derived from Human Embryonic Stem Cells by Honig, George R., Lu, Shi-Jiang, Feng, Qiang, Vida, Loyda N., Lee, Bao-Shiang, Lanza, Robert

“…Under culture conditions that promote hematopoietic differentiation, human embryonic stem cells (huESC) give rise to primitive erythroid cells that closely…”
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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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Effects in vitro of the proposed antisickling agent DBA by HONIG, GEORGE R, VIDA, LOYDA N, FERENC, CHRISTINE

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Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C by Honig, G R, Mason, R G, Tremaine, L M, Vida, L N

“…Silent carrier alpha-thalassemia was identified in two individuals, one with sickle-cell trait and the other hemoglobin (Hb) C trait. Both are parents of a…”
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Iron deficiency and sickle cell anemia by Rao, K R, Patel, A R, Honig, G R, Vida, L N, McGinnis, P R

“…In a patient with sickle cell anemia, iron deficiency was accompanied by hypochromic, microcytic RBCs, absence of bone marrow iron, and a low serum ferritin…”
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Hb RAMPA [α95(G2)Pro→Ser (α2)] IN A FAMILY OF EUROPEAN ANCESTRY: DNA ANALYSIS CONFIRMS THE C CG→T CG MUTATION AT CODON 95 OF THE α2-GLOBIN GENE; CLINICAL AND LABORATORY FEATURES by Hoyer, James D., Rachut, Eric, Kubik, Kathleen S., Jones, Richard T., Honig, George R., Vida, Loyda N., Fairbanks, Virgil F.

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Hb Rampa [alpha 95(G2)pro-->Ser (alpha 2)] in a family of European ancestry: DNA analysis confirms the CCG-->TCG mutation at codon 95 of the alpha 2-globin gene; clinical and laboratory features by Hoyer, James D, Rachut, Eric, Kubik, Kathleen S, Jones, Richard T, Honig, George R, Vida, Loyda N, Fairbank, Virgil F

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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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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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Hemoglobin Lincoln Park: A β δ Fusion (Anti-Lepore) Variant with an Amino Acid Deletion in the δ Chain-Derived Segment by Honig, George R., Shamsuddin, Mir, Mason, R. George, Vida, Loyda 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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610 α-THALASSEMIA SILENT CARRIER WITH HEMOGLOBINS S AND C by Honig, George R, Mason, R George, Tremalne, Larry, Vida, Loyda N

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611 UNBALANCED GLOBIN SYNTHESIS IN ANTI-LEPORE HEMOGLOBIN Oil ERYTHROID CELLS by Honig, George R, Tremaine, Larry, Mason, R George, Vida, Loyda N

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Hemoglobin Nigeria (α-81 Ser→CysJiA New Variant Associated With α-Thalassemia by Honig, George R., Shamsuddin, Mir, Mason, R. George, Vida, Loyda N., Tremaine, Larry M., Tarr, George E., Shahidi, Nasrollah T.

“…Hematologic evaluation of a Nigerian obstetrical patient disclosed the presence of sickle-cell trait as well as evidence of a hemoglobin α-chain abnormality…”
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Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome by Honig, G R, Koshy, M, Mason, R G, Vida, L N

“…Five American black patients, ages 1 to 16 years, with the sickle cell anemia-alpha-thalassemia syndrome are described. Each patient had persistent…”
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Three new variants of glucose-6-phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G-6-PD Lincoln Park, G-6-PD Arlington Heights, and G-6-PD West Town by Honig, G R, Habacon, E, Vida, L N, Matsumoto, F, Beutler, E

“…Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency was identified in three children who were evaluated because of chronic nonspherocytic hemolytic anemia…”
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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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Homozygous sickle cell disease with coexistent hereditary spherocytosis in three siblings by Maurer, H S, Vida, L N, Honig, G R

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Unbalanced globin chain synthesis by Hb Lincoln Park (anti-Lepore) reticulocytes by Honig, G R, Mason, R G, Tremaine, L M, Vida, L N

“…Hemoglobin synthesis was studied in vitro in reticulocytes from a patient with the anti-Lepore variant Hb Lincoln Park. Incorporation of L-leucine-3H into the…”
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