Search Results - "Raess, Philipp"

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    Prolonged hematologic toxicity following treatment with chimeric antigen receptor T cells in patients with hematologic malignancies by Nagle, Sarah J., Murphree, Catherine, Raess, Philipp W., Schachter, Levanto, Chen, Andy, Hayes‐Lattin, Brandon, Nemecek, Eneida, Maziarz, Richard T.

    Published in American journal of hematology (01-04-2021)
    “…Chimeric antigen receptor T‐cell therapy (CAR T) is a novel intervention for relapsed/refractory diffuse large B‐cell lymphoma (R/R DLBCL) and other…”
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    Molecular Discordance between Myeloid Sarcomas and Concurrent Bone Marrows Occurs in Actionable Genes and Is Associated with Worse Overall Survival by Werstein, Brian, Dunlap, Jennifer, Cascio, Michael J., Ohgami, Robert S., Fan, Guang, Press, Richard, Raess, Philipp W.

    Published in The Journal of molecular diagnostics : JMD (01-03-2020)
    “…Myeloid sarcoma is a rare, architecture-effacing proliferation of myeloid blasts localized to an extramedullary site, with or without concurrent bone marrow…”
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    The combination of NPM1, DNMT3A, and IDH1/2 mutations leads to inferior overall survival in AML by Dunlap, Jennifer B., Leonard, Jessica, Rosenberg, Mara, Cook, Rachel, Press, Richard, Fan, Guang, Raess, Philipp W., Druker, Brian J., Traer, Elie

    Published in American journal of hematology (01-08-2019)
    “…Acute myeloid leukemia (AML) is a genetically heterogeneous disease with a clinical course predicted by recurrent cytogenetic abnormalities and/or gene…”
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    Cutaneous Plasmacytosis and Idiopathic Multicentric Castleman Disease: A Spectrum of Disease? by Drissi, Madeeha, Dunlap, Rachel, Clayton, Lara, Raess, Philipp W., Mengden Koon, Stephanie, White, Kevin

    Published in The American journal of dermatopathology (01-04-2022)
    “…Cutaneous/systemic plasmacytosis (C/SP) is a plasma cell disorder characterized by reddish-brown patches, lymphadenopathy, and hypergammaglobulinemia. The…”
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    Going Skin Deep: Excavating a Diagnosis of Intravascular Large B Cell Lymphoma by Oppegard, Laura, O’Donnell, Matthew, Piro, Kevin, Shatzel, Joseph, Christian, Robert, Raess, Philipp W., Desai, Sima

    “…A fever of unknown origin is often pursued diagnostically under the framework of infectious, rheumatologic, and neoplastic causes. When encephalopathy ensues,…”
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    Vertical sleeve gastrectomy specimens have a high prevalence of unexpected histopathologic findings requiring additional clinical management by Raess, Philipp W., M.D., Ph.D, Baird-Howell, Marilyn, Aggarwal, Rajesh, M.D., Ph.D, Williams, Noel N., M.D, Furth, Emma E., M.D

    Published in Surgery for obesity and related diseases (01-09-2015)
    “…Abstract Background Laparoscopic vertical sleeve gastrectomy is used with increasing frequency as a therapeutic option for morbid obesity. Before the…”
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    Nipple leiomyoma: A rare neoplasm with a broad spectrum of histologic appearances by Hammer, Phoebe, White, Kevin, Mengden, Stephanie, Korcheva, Vessy, Raess, Philipp W.

    Published in Journal of cutaneous pathology (01-05-2019)
    “…Cutaneous leiomyomas are rare benign smooth‐muscle tumors. These lesions are distinguished based on their cell of origin and are subclassified as pilar…”
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    Choline Transporter Immunohistochemistry: An Effective Substitute for Acetylcholinesterase Histochemistry to Diagnose Hirschsprung Disease With Formalin-fixed Paraffin-embedded Rectal Biopsies by Kapur, Raj P, Raess, Philipp W, Hwang, Samuel, Winter, Conrad

    Published in Pediatric and developmental pathology (01-07-2017)
    “…Acetylcholinesterase enzymatic histochemistry (AChE EHC), which highlights abnormal cholinergic nerves in the mucosa of aganglionic bowel, has been used for…”
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    Histology-Independent Signature Distinguishes Kikuchi-Fujimoto Disease/Systemic Lupus Erythematosus–Associated Lymphadenitis From Benign and Malignant Lymphadenopathies by Scott, Gregory D, Kumar, Jyoti, Oak, Jean S, Boyd, Scott D, Raess, Philipp W, Gratzinger, Dita A

    Published in American journal of clinical pathology (01-08-2020)
    “…Abstract Objectives Kikuchi-Fujimoto disease (KFD) and systemic lupus erythematosus (SLE) are benign entities with histologic features that raise concern about…”
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