SA Feig, GB Segel… - Chronic Complex Diseases of …, 2011 - books.google.com ... This is especially true for patients with congenital forms of aplasia, who are at increased risk of developing leukemia, but it is important to be certain that a sibling donor is unaffected, before proceeding with HSCT for congenitalaplasticanemia. ... Related articles
[HTML] from hematologylibrary.orgD Heckl, DC Wicke, MH Brugman… - …, 2011 - bloodjournal.hematologylibrary.org ... 2–4. Loss of MPL function results in aplasticanemia and thrombocytopenia, a disease termed congenital amegakaryocytic thrombocytopenia (CAMT). 5 Untreated CAMT patients die early in childhood, and the only curative therapy ... Cited by 2 - Related articles - All 2 versions
[HTML] from haematologica.comR Bizzetto, C Bonfim, V Rocha, G Socie… - …, 2011 - haematologica.com ... was given to five patients with DBA, five with DC, six with CAMT, 13 with SCN, and one with SDS, while reduced intensity conditioning was given to three patients with DBA, one with DC, seven with CAMT, two with SCN and one with unclassified congenitalaplasticanemia. ... Cited by 1 - Related articles - All 8 versions
[HTML] from virologyj.comB Rauff, M Idrees, SAR Shah, S Butt, AM Butt… - Virology …, 2011 - virologyj.com ...Aplasticanemia, acquire or congenitalanemia associated with hypoplastic "fatty or empty" bone marrow and global dyshematopoiesis, has been first described by Paul Ehrlich in year 1888 [1]. The pathophysiology is believed to be idiopathic [2] or immune-mediated ... Related articles - Cached - All 4 versions
T Hünig - US Patent 7,868,143, 2011 - Google Patents ... karyocytes). The fifth group are the aplastic anemias or bone marrow failure with aplasia/hypoplasia of the bone marrow and pan- cytopenia (stem cell disease). A congenitalaplasticanemia is for instance the Fanconi's anemia. More ... Related articles - All 4 versions
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