Diseases

Waldenström and IgM disorders

4 papers and 2 abstracts co-authored by Raphael E. Szalat. Current lab members are shown in bold.

Papers 4

  1. 2022

    Light chain amyloidosis associated with Waldenström macroglobulinemia: treatment and survival outcomes

    Gustine JN, Szalat RE, Staron A, Joshi T, Mendelson L, Sloan JM, Sanchorawala V

    Haematologica108(6):1680-1684DOI: Light chain amyloidosis associated with Waldenström macroglobulinemia: treatment and survival outcomesPubMed: Light chain amyloidosis associated with Waldenström macroglobulinemia: treatment and survival outcomes

  2. 2021

    IgM-MM is predominantly a pre–germinal center disorder and has a distinct genomic and transcriptomic signature from WM

    Bazarbachi AH, Avet-Loiseau H, Szalat R, …, Samur MK

    Blood138(20):1980-1985DOI: IgM-MM is predominantly a pre–germinal center disorder and has a distinct genomic and transcriptomic signature from WMPubMed: IgM-MM is predominantly a pre–germinal center disorder and has a distinct genomic and transcriptomic signature from WM

  3. 2015

    Bortezomib produces high hematological response rates with prolonged renal survival in monoclonal immunoglobulin deposition disease

    Cohen C, Royer B, Javaugue V, Szalat R, …, Bridoux F

    Kidney International88(5):1135-1143DOI: Bortezomib produces high hematological response rates with prolonged renal survival in monoclonal immunoglobulin deposition diseasePubMed: Bortezomib produces high hematological response rates with prolonged renal survival in monoclonal immunoglobulin deposition disease

  4. 2014

    Clinico‐biological characteristics and treatment of type I monoclonal cryoglobulinaemia: a study of 64 cases

    Harel S, Mohr M, Jahn I, …, Szalat R, …, Fermand J

    British Journal of Haematology168(5):671-678DOI: Clinico‐biological characteristics and treatment of type I monoclonal cryoglobulinaemia: a study of 64 casesPubMed: Clinico‐biological characteristics and treatment of type I monoclonal cryoglobulinaemia: a study of 64 cases

Abstracts & posters 2

  1. 2020

    Genomic and Transcriptomic Characterization of IgM Multiple Myeloma Identifies a Pre-Germinal Center Plasma Cell Disorder with Immature B-Cell Transcription-Factor Signature

    Bazarbachi AH, Avet-Loiseau H, Hunter ZR, Szalat R, …, Munshi NC

    Blood136(Supplement 1):7-8DOI: Genomic and Transcriptomic Characterization of IgM Multiple Myeloma Identifies a Pre-Germinal Center Plasma Cell Disorder with Immature B-Cell Transcription-Factor Signature

  2. 2013

    IgM Hevylite Assay as a Biomarker of Clinical Outcome in Patients with Anti-MAG Neuropathy: P-457

    ARNULF B, BENGOUFA D, LAZARETH A, SZALAT R, MALPHETTES M, et al.

    Clinical Lymphoma, Myeloma & Leukemia13:s254-s255