Search Results - "Alexieff, Marilyn J."

Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients by Markert, M. Louise, Sarzotti, Marcella, Ozaki, Daniel A., Sempowski, Gregory D., Rhein, Maria E., Hale, Laura P., Le Deist, Francoise, Alexieff, Marilyn J., Li, Jie, Hauser, Elizabeth R., Haynes, Barton F., Rice, Henry E., Skinner, Michael A., Mahaffey, Samuel M., Jaggers, James, Stein, Leonard D., Mill, Michael R.

“…Complete DiGeorge syndrome is a fatal condition in which infants have no detectable thymus function. The optimal treatment for the immune deficiency of…”
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Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants by Markert, M. Louise, Devlin, Blythe H., Alexieff, Marilyn J., Li, Jie, McCarthy, Elizabeth A., Gupton, Stephanie E., Chinn, Ivan K., Hale, Laura P., Kepler, Thomas B., He, Min, Sarzotti, Marcella, Skinner, Michael A., Rice, Henry E., Hoehner, Jeffrey C.

“…The purpose of this study was to characterize a large group of infants with complete DiGeorge anomaly and to evaluate the ability of thymus transplantation to…”
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Complete DiGeorge syndrome: Development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases by Louise Markert, M, Alexieff, Marilyn J, Li, Jie, Sarzotti, Marcella, Ozaki, Daniel A, Devlin, Blythe H, Sempowski, Gregory D, Rhein, Maria E, Szabolcs, Paul, Hale, Laura P, Buckley, Rebecca H, Coyne, Katharine E, Rice, Henry E, Mahaffey, Samuel M, Skinner, Michael A

“…Five patients with DiGeorge syndrome presented with infections, skin rashes, and lymphadenopathy after the newborn period. T-cell counts and function varied…”
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Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome by Markert, M. Louise, Alexieff, Marilyn J., Li, Jie, Sarzotti, Marcella, Ozaki, Daniel A., Devlin, Blythe H., Sedlak, Debra A., Sempowski, Gregory D., Hale, Laura P., Rice, Henry E., Mahaffey, Samuel M., Skinner, Michael A.

“…Complete DiGeorge syndrome is a fatal congenital disorder characterized by athymia, hypoparathyroidism, and heart defects. Less than half of patients are 22q11…”
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