Zobrazeno 1 - 10
of 85
pro vyhledávání: '"P. J. Fialkow"'
Publikováno v:
Journal of Intellectual Disability Research. 15:177-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f50ea61f0b25cef06c066ef3a7d48943
https://doi.org/10.1111/j.1365-2788.1971.tb01155.x
https://doi.org/10.1111/j.1365-2788.1971.tb01155.x
Publikováno v:
Blood. 77:1415-1417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ec4979bd19134ccc9b88bbb423b3592
https://doi.org/10.1182/blood.v77.7.1415.bloodjournal7771415
https://doi.org/10.1182/blood.v77.7.1415.bloodjournal7771415
Publikováno v:
Leukemia. 7(8)
The Ph chromosome abnormality is involved in the pathogenesis of almost all patients with chronic myelocytic leukemia (CML). Previous studies on the B-lymphoid cell lineage in two patients with Ph-positive CML suggest that there may also be a clonal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::877a1ac643a46bb12dd050026f0d18f3
https://pubmed.ncbi.nlm.nih.gov/8350616
https://pubmed.ncbi.nlm.nih.gov/8350616
Autor:
J W, Singer, P J, Fialkow
Publikováno v:
Leukemia. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::04ca212b5276156a689f9cab58c8ef6a
https://pubmed.ncbi.nlm.nih.gov/1548937
https://pubmed.ncbi.nlm.nih.gov/1548937
Autor:
P J, Fialkow
Publikováno v:
Verhandlungen der Deutschen Gesellschaft fur Pathologie. 74
Studies with G6PD and molecular probes indicate that the myeloid leukemias and the chronic myeloproliferative disorders are clonal diseases. The G6PD data indicate that chronic myelogenous leukemia, polycythemia vera and essential thrombocythemia inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e14be93d0b963db30ffe7021e829a3a
https://pubmed.ncbi.nlm.nih.gov/1708632
https://pubmed.ncbi.nlm.nih.gov/1708632
Autor:
ThomasG. Rudd, LawrenceY. Agoda, JohnD. Denney, JeanI. Bryant, LeonA. Phillips, P. J. Fialkow, Jovan Milutinovic
Publikováno v:
The Lancet. 315:1203-1206
Because the onset of symptoms in patients with autosomal dominant polycystic kidney disease is generally delayed until adulthood, genetic counselling is imprecise. In an attempt to identify patients early, 261 offspring of subjects with the gene for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7b0249b2a1ec4f6a998e668f57e3e23
https://doi.org/10.1016/s0140-6736(80)91674-8
https://doi.org/10.1016/s0140-6736(80)91674-8
Publikováno v:
Experimental Cell Research. 89:275-282
Multiple lymphoblastoid cell lines were established from each of seven Burkitt lymphoma biopsies and from tonsils, removed from four patients with chronic tonsillitis. The cellular origin of the lines was studied using as markers the pattern of immun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::557907da3448711036a01f860eef3b46
https://doi.org/10.1016/0014-4827(74)90791-5
https://doi.org/10.1016/0014-4827(74)90791-5
Autor:
Robert W. McGuffin, A Keating, Jean E. Sanders, R Ramberg, J. W. Singer, P. J. Fialkow, George E. Sale, Thomas Ed
Publikováno v:
Scopus-Elsevier
This article describes the course of a patient who received an allogeneic marrow graft from his HLA-identical sister for acute lymphoblastic leukemia in second remission. In the second month after grafting, marrow aspirates showed the presence of 7%-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c62ae0d12ba983a1ad1392b1e5f792bf
https://doi.org/10.1182/blood.v62.4.869.bloodjournal624869
https://doi.org/10.1182/blood.v62.4.869.bloodjournal624869
Publikováno v:
Blood. 56:70-73
It has been shown with glucose 6-phosphate dehydrogenase (G-6-PD) mosaicism that Ph1-positive chronic myelogenous leukemia (CML) is a clonal disease that involves multipotent hematopoietic stem cells. We now report G-6-PD studies of a 79-yr-old woman
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3189ee2c198325d1179a9a0a8157f3e5
https://doi.org/10.1182/blood.v56.1.70.bloodjournal56170
https://doi.org/10.1182/blood.v56.1.70.bloodjournal56170
Publikováno v:
Blood. 53:264-268
Granulocytic colonies grown in culture from marrow and peripheral blood from five patients with Ph1-positive CML and heterozygous at the G-6-PD locus were analyzed for G-6-PD in order to identify CFU-C that do not arise from the CML clone. The patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8206d46062dbf10721b9683667f0492
https://doi.org/10.1182/blood.v53.2.264.bloodjournal532264
https://doi.org/10.1182/blood.v53.2.264.bloodjournal532264