Zobrazeno 1 - 10
of 20
pro vyhledávání: '"L N Vida"'
Publikováno v:
American Journal of Hematology. 34:199-203
Fifteen individuals among four generations of a family of English ancestry demonstrated elevated hemoglobin levels accompanied by leftward-shifted whole blood oxygen equilibrium curves. Five of the affected family members have required phlebotomies f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c711487ab53001e671d47cff98e1f976
https://doi.org/10.1002/ajh.2830340308
https://doi.org/10.1002/ajh.2830340308
Publikováno v:
American journal of hematology. 58(1)
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 reticulocyte count was elevated (4.3%), and erythroblasts were present in his peripheral blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a73d74f06f7010b764c6cb8bb3106f8b
https://pubmed.ncbi.nlm.nih.gov/9590152
https://pubmed.ncbi.nlm.nih.gov/9590152
Publikováno v:
Blood. 89(6)
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 animal species. In patients who are homozygous for the sickle Hb (HbS) mutation, transfusion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c75c5069a2ca20edd4f60938afd0f0d9
https://pubmed.ncbi.nlm.nih.gov/9058739
https://pubmed.ncbi.nlm.nih.gov/9058739
Publikováno v:
The Journal of biological chemistry. 265(1)
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 formation. In DEAE-cellulose chromatography, the variant hemoglobin co-eluted with Hb A; a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b1423d5825d4bfbbf2e7762029ca9e6
https://pubmed.ncbi.nlm.nih.gov/2294098
https://pubmed.ncbi.nlm.nih.gov/2294098
Publikováno v:
Blood. 55:655-660
Hemoglobin variants having electrophoretic mobility more rapid than that of HbA were identified in combination with sickle hemoglobin in two patients at the Cook County Hospital. Neither individual had symptomatic hematologic disease. In one patient,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67fbd22713bc9a30844086c71ac2ce6b
https://doi.org/10.1182/blood.v55.4.655.bloodjournal554655
https://doi.org/10.1182/blood.v55.4.655.bloodjournal554655
Publikováno v:
Proceedings of the National Academy of Sciences. 75:1475-1479
An electrophoretically slow-moving hemoglobin variant was identified in three members of a family originating from Southern Mexico. The variant, Hb Lincoln Park, made up approximately 14% of the total hemoglobin and appeared to have normal stability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::656f6ce5cbe689d7fd291b81ee247355
https://doi.org/10.1073/pnas.75.3.1475
https://doi.org/10.1073/pnas.75.3.1475
Publikováno v:
Blood. 55:655-660
Hemoglobin variants having electrophoretic mobility more rapid than that of HbA were identified in combination with sickle hemoglobin in two patients at the Cook County Hospital. Neither individual had symptomatic hematologic disease. In one patient,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a261d1351cc287176121cde4146f0b55
https://doi.org/10.1182/blood.v55.4.655.655
https://doi.org/10.1182/blood.v55.4.655.655
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Protein Structure. 626:424-431
Hemoglobin Milledgeville, a new hemoglobin structural variant, was identified in three members of a black American family. The oxygen affinity of blood and hemoglobin samples from the affected individuals was markedly increased (p50 O2 of whole blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1cbec37fe1115f3a65b5ee6fd8a85cd
https://doi.org/10.1016/0005-2795(80)90138-5
https://doi.org/10.1016/0005-2795(80)90138-5
Publikováno v:
Blood. 55(1)
Hematologic evaluation of a Nigerian obstetrical patient disclosed the presence of sickle-cell trait as well as evidence of a hemoglobin alpha-chain abnormality. Hemoglobins containing the variant alpha-chain were isolated by DEAE-cellulose column ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b7c72b4e95be040f3fafbc57942c0b1
https://pubmed.ncbi.nlm.nih.gov/7350933
https://pubmed.ncbi.nlm.nih.gov/7350933
Publikováno v:
Biochimica et biophysica acta. 626(2)
Hemoglobin Milledgeville, a new hemoglobin structural variant, was identified in three members of a black American family. The oxygen affinity of blood and hemoglobin samples from the affected individuals was markedly increased (p50 O2 of whole blood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c1bbc12d9769e9e8bca62871cce58e2
https://pubmed.ncbi.nlm.nih.gov/7213661
https://pubmed.ncbi.nlm.nih.gov/7213661