Search Results - "Junagade, Pritesh"
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A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects
Published in Human mutation (01-12-2021)“…Fanconi anemia (FA) is a rare autosomal or X‐linked genetic disorder characterized by chromosomal breakages, congenital abnormalities, bone marrow failure…”
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Rituximab in Children with Autoimmune Thrombocytopenia Complicating Underlying Congenital or Acquired Immunodeficiency State
Published in Blood (16-11-2006)“…Rituximab (chimeric anti-CD20 monoclonal antibody) has been reported to be effective in various autoimmune conditions, especially in autoimmune cytopenias, but…”
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Second Reduced Intensity Transplants Are Effective and Well Tolerated in Older Patients with Relapsed Myeloid Malignancies. A Single Centre Report
Published in Blood (16-11-2005)“…Previous reports of second allografts for relapsed leukaemia involved either children or young adults. However, the majority of myeloid leukaemias present in…”
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