Výsledky vyhledávání - "E R, Giblett"

Transfusions shortly before HLA-matched marrow transplantation for leukemia are associated with a decrease in chronic graft-versus-host disease

Autor: G C, deGast, P G, Beatty, D, Amos, E M, Mickelson, K M, Sullivan, J E, Anderson, E R, Giblett, F, Appelbaum, R, Storb, H J, Deeg

Publikováno v: Bone marrow transplantation. 7(4)

The effect of random red cell transfusions given shortly before allogeneic bone marrow transplantation (BMT) was evaluated in 969 leukemic patients transplanted from an HLA-identical sibling donor. Patients were divided into two groups: 501 who recei

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::47678bc44e77edd60e959cb32a88de84
https://pubmed.ncbi.nlm.nih.gov/2070135

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Aplastic anemia treated by allogeneic bone marrow transplantation: a report on 49 new cases from Seattle

Autor: R, Storb, E D, Thomas, P L, Weiden, C D, Buckner, R A, Clift, A, Fefer, L P, Fernando, E R, Giblett, B W, Goodell, F L, Johnson, K G, Lerner, P E, Neiman, J E, Sanders

Publikováno v: Blood. 48:817-841

Forty-nine patients with severe aplastic anemia, 33 due to unknown cause, 11 drug or chemical related, 2 associated with hepatitis, 1 with paroxysmal nocturnal hemoglobinuria, and 2 possibly associated with Fanconi syndrome did not show recovery afte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd1f67d5f21dc2018a4739c2777e52ac
https://doi.org/10.1182/blood.v48.6.817.bloodjournal486817

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Clinical manifestations of familial 13;18 translocation

Autor: M L Kistenmacher, E R Giblett, W A Blattner, H H Punnett, S Tsai

Publikováno v: Journal of Medical Genetics. 17:373-379

Female first cousins, aged 21 and 2 1/2 years, with many of the characteristic features of trisomy 18, were found to have identical unbalanced translocations, 46,XX,--13, + der(13)t(13;18) (p13;q12)mat. Clinical features of another cousin, two uncles

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0341e546d07a170c8597fda1a0e11a4e
https://doi.org/10.1136/jmg.17.5.373

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Haemoglobin M Hyde Park occurring as a fresh mutation: diagnostic, structural, and genetic considerations

Autor: P E Nute, J C Detter, R Chard, E R Giblett, G Stamatoyannopoulos

Publikováno v: Journal of Medical Genetics. 13:142-147

Hb M Hyde Park disease was detected in a girl who for several years was thought to have cyanotic heart disease. The problems of recognizing the condition are outlined and clues to diagnosis are discussed. Evidence for heme loss from the aberrant beta

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f86f84fcbb664ab8ef8f63d82388c9a
https://doi.org/10.1136/jmg.13.2.142

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Red cell enzyme polymorphisms in the Greek populations

Autor: A. Thomakos, E. R. Giblett, George Stamatoyannopoulos

Publikováno v: Humangenetik. 27:23-30

The frequency of variant forms of 6 red cell enzymes, adenylate kinase, adenosine deaminase, phosphoglucomutase, acid phosphatase, 6-phosphogluconate dehydrogenase and glutathione reductase, were determined in 9 Greek populations. The frequencies of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed5ea51e8fd15ca0dbad983e1ac19183
https://doi.org/10.1007/bf00283500

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A Family with the Rare Red Cell Antigens Wraand ‘Super’ Sda

Autor: M Lewis, June Gavin, Arthur G. Steinberg, Hiroko Kaita, E R Giblett, Patricia Tippett, Ruth Sanger, B. Chown

Publikováno v: Vox Sanguinis. 25:336-340

A family is recorded in which the two rare antigens ‘super’ Sid, or ‘super’ Sda, and Wra are present. The linkage count between the two characters is six non-recombinants, for which the lod score at θ =0.00 is 1.806. This is tantalizingly su

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::751d4ed8c18067332df44fd5650237ca
https://doi.org/10.1111/j.1423-0410.1973.tb04381.x

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