Search Results - "Greiner, Robert J."

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    Assessment of chimerism by next generation sequencing: A comparison to STR/qPCR methods by Brow, Darren, Shike, Hiroko, Kendrick, Jasmine, Pettersson, Linnea, Mineishi, Shin, Claxton, David F., Wirk, Baldeep, Cioccio, Joseph, Greiner, Robert J., Viswanatha, David, Kharfan-Dabaja, Mohamed A., Li, Zhuo, Tyler, Jennifer, Elrefaei, Mohamed

    Published in Human immunology (01-05-2024)
    “…Chimerism analysis is used to evaluate patients after allogeneic hematopoietic stem cell transplant (allo-HSCT) for engraftment and minimal measurable residual…”
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    Journal Article
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    Suprasellar central nervous system ganglioneuroblastoma: a case in a 9-year-old child and review of the literature by Mrowczynski, Oliver D., Lane, Jessica R., Specht, Charles S., Greiner, Robert J., Iantosca, Mark R., Rizk, Elias B.

    Published in Child's nervous system (01-11-2020)
    “…Purpose Intracranial ganglioneuroblastomas are incredibly rare neuroectodermal tumors with only 8 described cases total, 5 of those having imaging findings…”
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    Reduced frequency of CD56 dim CD16 pos natural killer cells in pediatric systemic inflammatory response syndrome/sepsis patients by Halstead, E Scott, Carcillo, Joseph A, Schilling, Bastian, Greiner, Robert J, Whiteside, Theresa L

    Published in Pediatric research (01-10-2013)
    “…Sepsis continues to be a leading cause of death in infants and children. Natural killer (NK) cells serve as a bridge between innate and adaptive immunity, yet…”
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    Intracranial malignant peripheral nerve sheath tumor variant: an unusual neurovascular phenotype sarcoma case invading through the petrous bone by Mrowczynski, Oliver D., Greiner, Robert J., Kapadia, Malika, Fanburg-Smith, Julie C., Iantosca, Mark R., Rizk, Elias B.

    Published in Child's nervous system (01-08-2018)
    “…Introduction Intracranial malignant peripheral nerve sheath tumor (MPNST) is exceedingly rare. Previously reported cases of intracranial MPNST have been…”
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    Radiation Necrosis Following Proton Beam Therapy in the Pediatric Population: a Case Series by Davanzo, Justin, Greiner, Robert J, Barbour, Mustafa, Rizk, Elias

    Published in Curēus (Palo Alto, CA) (19-10-2017)
    “…Radiation necrosis after proton beam radiotherapy in the pediatric population is a finding that should be evaluated. We present two cases of radiation necrosis…”
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    Synchronous occurrence of metastatic Wilms tumor and ganglioneuroma by Moran, Cassandra, Greiner, Robert J., Mardam-Bey III, Sami W., Hollingsworth, Caroline L., Kulbacki, Evan, Wechsler, Daniel S.

    Published in Pediatric blood & cancer (01-09-2010)
    “…We describe a 4‐year‐old female patient with a persistent paraspinal mass following chemotherapy for Wilms tumor. A discordant response to chemotherapy…”
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    Utilization of Total Body Irradiation Is Not Necessary for Unrelated Donor Umbilical Cord Blood Transplants: a Single-Center Experience by Pu, Jeffrey J., Miller, Elizabeth L, Berg, Arthur, Comito, Melanie, Greiner, Robert J., Ehmann, W. Christopher, Claxton, David F., Rybika, Witold B

    Published in Blood (06-12-2014)
    “…▪ Background: Umbilical cord blood (UCB) is rich in primitive hematopoietic stem cells (HSC) and progenitor cells that can reconstitute the hematopoietic…”
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    Reduced frequency of CD56dim CD16pos natural killer cells in pediatric systemic inflammatory response syndrome/sepsis patients by Halstead, E. Scott, Carcillo, Joseph A., Schilling, Bastian, Greiner, Robert J., Whiteside, Theresa L.

    Published in Pediatric research (15-07-2013)
    “…Background: Sepsis continues to be a leading cause of death in infants and children. Natural killer (NK) cells serve as a bridge between innate and adaptive…”
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    Journal Article
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    Complete Responses in Patients with Autoimmune Lymphoproliferative Syndrome (ALPS) Using the mTOR Inhibitor Sirolimus (rapamycin) by Teachey, Davi d T., Greiner, Robert J, Schwabe, Dirk, Bleesing, Jack, Manno, Catherine Scott, Sullivan, Kathleen, Wechsler, Daniel S., Grupp, Stephan A.

    Published in Blood (16-11-2008)
    “…Autoimmune lymphoproliferative syndrome (ALPS) is a rare disorder of abnormal lymphocyte survival caused by defective Fas-mediated apoptosis. Patients with…”
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