We are improving our search experience. To check which content you have full access to, or for advanced search, go back to the old search.

Search

Please fill in this field.
Filters applied:
Biomedicine

Search Results

Showing 1-20 of 1,607 results

  2. A Novel Mutation Leading to Wiskott-Aldrich Syndrome in an Ethiopian Boy: a Case Report and a Review of Literature

    Wiskott–Aldrich syndrome is an X-linked recessive primary immune-deficiency disorder very rarely reported from black African children. A 12-year old...

    Tinsae Alemayehu, Donald C. Vinh in Journal of Clinical Immunology
    Article 13 April 2023

  5. Inadequate Activation of γδT- and B-cells in Patient with Wiskott-Aldrich Syndrome (WAS) Portrayed by TRG and IGH Repertoire Analyses

    Patients with Wiskott-Aldrich syndrome (WAS) harbor mutations in the WAS gene and suffer from immunodeficiency, microthrombocytopenia, and eczema....

    Dahlia Palevski, Amos Simon, ... Yu Nee Lee in Journal of Clinical Immunology
    Article Open access 31 August 2022

  6. Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott–Aldrich syndrome

    Patients with Wiskott–Aldrich syndrome (WAS) lacking a human leukocyte antigen-matched donor may benefit from gene therapy through the provision of...

    A. Magnani, M. Semeraro, ... M. Cavazzana in Nature Medicine
    Article Open access 24 January 2022

  9. Acquired Hemophilia A in Wiskott–Aldrich Syndrome

    Tingyan He, Ke Cao, ... Jun Yang in Journal of Clinical Immunology
    Article 03 March 2021

  10. Wiskott-Aldrich Syndrome Deficiency

    Michel J. Massaad in Encyclopedia of Medical Immunology
    Reference work entry 2020

  13. Identification of a novel WAS mutation in a South African patient presenting with atypical Wiskott-Aldrich syndrome: a case report

    Background

    The X-linked recessive primary immunodeficiency disease (PIDD) Wiskott-Aldrich syndrome (WAS) is identified by an extreme susceptibility to...

    Brigitte Glanzmann, Marlo Möller, ... Craig J. Kinnear in BMC Medical Genetics
    Article Open access 05 June 2020

  16. Quality of Life of Patients with Wiskott Aldrich Syndrome and X-Linked Thrombocytopenia: a Study of the Primary Immune Deficiency Consortium (PIDTC), Immune Deficiency Foundation, and the Wiskott-Aldrich Foundation

    Background

    We undertook a study to determine the impact of Wiskott Aldrich Syndrome (WAS) and X-linked thrombocytopenia (XLT) and their therapies upon...

    Ami J. Shah, Robert Sokolic, ... Morton J. Cowan in Journal of Clinical Immunology
    Article 16 October 2019

  19. Lymphocytes Utilize Somatic Mutations, Epigenetic Silencing, and the Proteasome to Escape Truncated WASP Expression

    Wiskott-Aldrich Syndrome Protein (WASP) deficiency causes Wiskott-Aldrich Syndrome (WAS), a sex-linked disorder characterized by combined...

    Caroline Khanna, Carole Le Coz, ... Neil Romberg in Journal of Clinical Immunology
    Article 12 February 2022

  20. Non-osteopenic Bone Pathology After Allo-hematopoietic Stem Cell Transplantation in Patients with Inborn Errors of Immunity

    Purpose

    There is a lack of data on post-HSCT non-osteopenic bone pathology specifically for children with inborn errors of immunity (IEI). We...

    Zainab M. Golwala, Nikita Gireesh Bhat, ... Reem Elfeky in Journal of Clinical Immunology
    Article Open access 17 March 2023
Did you find what you were looking for? Share feedback.