Zobrazeno 1 - 10 of 118 pro vyhledávání: '"Virgil F, Fairbanks"'
1
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency
Autor: Virgil F. Fairbanks, Steven L. Allen, James D. Hoyer, Ernest Beutler, Kathleen S. Kubik, Carol West
Publikováno v: American Journal of Hematology. 75:205-208
A 28-year-old asymptomatic male of Iranian Jewish (Meshadi) heritage was found on routine exam to have an erythrocytosis (RBC = 6.22 × 1012/l, Hgb = 19.2 g/dl, Hct = 58.9%). Splenomegaly was absent on physical exam. There was no family history of er
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6d8268d9c4a2870bfb2648ea1138419
https://doi.org/10.1002/ajh.20014
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4
Hereditary Red Blood Cell Disorders in Middle Eastern Patients
Autor: James D. Hoyer, David P. Steensma, Virgil F. Fairbanks
Publikováno v: Mayo Clinic Proceedings. 76:285-293
Hereditary disorders of erythrocytes are common in many areas of the world, including the Middle East. In some regions of the Middle East more than 10% of the population are carriers of a gene for one of these conditions. When patients from the Middl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9cb852fa0c7c930aeab722c5c52ea2b
https://doi.org/10.4065/76.3.285
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5
Hb DARTMOUTH [α66(E15)Leu → Pro (α2) (CTG → CCG)]: A NOVEL α2-GLOBIN GENE MUTATION ASSOCIATED WITH SEVERE NEONATAL ANEMIA WHEN INHERITED IN TRANS WITH SOUTHEAST ASIAN α-THALASSEMIA-1
Autor: Robert B. Fairweather, William H. Edwards, Sara Chaffee, Kathleen S. Kubik, James D. Hoyer, Virgil F. Fairbanks, Karen Snow, Kim L. McBride
Publikováno v: Hemoglobin. 25:375-382
We report a novel mutation at alpha66(E15)Leu-->Pro (alpha2) (CTG-->CCG), that we have named Hb Dartmouth for the medical center at which the patients were cared for, in monozygotic twins who also inherited the Southeast Asian alpha-thalassemia-1 del
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3f723d4ef88f0fa78781f612b0d9443
https://doi.org/10.1081/hem-100107874
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6
Molecular characterization of a case of atransferrinemia
Autor: Terri Gelbart, Mark A. Fernandez, Pauline Lee, Ernest Beutler, Renee Trevino, Virgil F. Fairbanks
Publikováno v: Blood. 96:4071-4074
Hereditary atransferrinemia is a rare but instructive disorder that has previously been reported in only 8 patients in 6 families. It is characterized by microcytic anemia and by iron loading, and can be treated effectively by plasma infusions. We no
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c9ba92b52a6cf3c22590269898f8c0b5
https://doi.org/10.1182/blood.v96.13.4071
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7
Molecular characterization of a case of atransferrinemia
Autor: Ernest Beutler, Terri Gelbart, Pauline Lee, Reneé Trevino, Mark A. Fernandez, Virgil F. Fairbanks
Publikováno v: Blood. 96:4071-4074
Hereditary atransferrinemia is a rare but instructive disorder that has previously been reported in only 8 patients in 6 families. It is characterized by microcytic anemia and by iron loading, and can be treated effectively by plasma infusions. We no
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24cc38c8ccdd5f0a444d537d762fe9c1
https://doi.org/10.1182/blood.v96.13.4071.h8004071_4071_4074
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8
Normal ranges for packed cell volume and hemoglobin concentration in adults: relevance to ‘apparent polycythemia’
Autor: Ayalew Tefferi, Virgil F. Fairbanks
Publikováno v: European Journal of Haematology. 65:285-296
Published data from Europe and North America indicate that for non-iron-deficient adult Caucasian males, the normal mean packed cell volume (PCV) is 0.46 and the 2.5-97.5 percentile interval is 04.0-0.53. Corresponding values for adult Caucasian fema
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a5d993507e1507a944cea6ba1868bd79
https://doi.org/10.1034/j.1600-0609.2000.065005285.x
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9
Update on Hereditary Hemochromatosis and the HFE Gene
Autor: Stephen N. Thibodeau, David J. Brandhagen, Kenneth P. Batts, Virgil F. Fairbanks
Publikováno v: Mayo Clinic Proceedings. 74:917-921
Hereditary hemochromatosis (HHC) is the most common inherited single gene disorder in people of northern European descent. Hereditary hemochromatosis is characterized by increased intestinal absorption of iron leading to its deposition into multiple
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fe2ef72a9b977707c9f357b82365eac
https://doi.org/10.4065/74.9.917
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10
Polycythemia Vera: The Packed Cell Volume and The Curious Logic of The Red Cell Mass
Autor: Virgil F. Fairbanks
Publikováno v: Hematology. 4:381-395
Since the first systematic blood volume studies of polycythemia in the 1920s, measurement of blood volume and red cell mass (RCM) has become routine. However, the radionuclide-labeling methods promulgated by the International Committee for Standardiz
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::127b1b253f55f7ca006a471092c11c3d
https://doi.org/10.1080/10245332.1999.11746463
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