How I manage patients with Wiskott Aldrich syndrome

Treosulfan and Fludarabine Conditioning for Hematopoietic Stem Cell Transplantation in Children with Primary Immunodeficiency: UK Experience

(2018) Mary A. Slatter et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

HSCT for PID: not just for children

(2018) Blachy J. Dávila Saldaña   BLOOD

Screening for Wiskott-Aldrich syndrome by flow cytometry

(2018) Samuel C.C. Chiang et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

One hundred percent survival after transplantation of 34 patients with Wiskott-Aldrich syndrome over 20 years

(2018) Reem Ahmed Elfeky et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Bleeding and splenectomy in Wiskott-Aldrich syndrome: A single-centre experience

(2018) Elizabeth Rivers et al.   Journal of Allergy and Clinical Immunology-In Practice

Diagnosis of platelet function disorders: A standardized, rational, and modular flow cytometric approach

(2017) Oliver Andres et al.   PLATELETS

Wiskott-Aldrich syndrome protein regulates autophagy and inflammasome activity in innate immune cells

(2017) Pamela P. Lee et al.   Nature Communications

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease

(2017) Walter H. A. Kahr et al.   Nature Communications

FOXP3+ Tregs require WASP to restrain Th2-mediated food allergy

(2016) Willem S. Lexmond et al.   JOURNAL OF CLINICAL INVESTIGATION

Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia

(2015) A. J. Gerrits et al.   BLOOD

Outcomes Following Gene Therapy in Patients With Severe Wiskott-Aldrich Syndrome

(2015) Salima Hacein-Bey Abina et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Food allergy in patients with primary immunodeficiency diseases: Prevalence within the US Immunodeficiency Network (USIDNET)

(2015) Karen S. Tuano et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

B-cell reconstitution after lentiviral vector–mediated gene therapy in patients with Wiskott-Aldrich syndrome

(2015) Maria Carmina Castiello et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Wiskott-Aldrich Syndrome in a Girl Caused by Heterozygous WASP Mutation and Extremely Skewed X-Chromosome Inactivation: A Novel Association with Maternal Uniparental Isodisomy 6

(2015) Tomohito Takimoto et al.   Neonatology

Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation

(2015) Da-Wei Liu et al.   PEDIATRIC BLOOD & CANCER

Wiskott-Aldrich syndrome iPS cells produce megakaryocytes with defects in cytoskeletal rearrangement and proplatelet formation

(2015) Praewphan Ingrungruanglert et al.   THROMBOSIS AND HAEMOSTASIS

Gene Therapy for Wiskott-Aldrich Syndrome--Long-Term Efficacy and Genotoxicity

(2014) C. J. Braun et al.   Science Translational Medicine

Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome

(2013) A. Aiuti et al.   SCIENCE

Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome

(2012) N. Mahlaoui et al.   BLOOD

Wiskott–Aldrich syndrome with IgA nephropathy: a case report and literature review

(2012) Chia-Hung Liu et al.   INTERNATIONAL UROLOGY AND NEPHROLOGY

A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP

(2012) Gaetana Lanzi et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Development of IgA nephropathy-like glomerulonephritis associated with Wiskott–Aldrich syndrome protein deficiency

(2011) M. Shimizu et al.   CLINICAL IMMUNOLOGY

Occurrence of Aortic Aneurysms in 5 Cases of Wiskott-Aldrich Syndrome

(2011) I. Pellier et al.   PEDIATRICS

X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options

(2010) M. H. Albert et al.   BLOOD

Wiskott-Aldrich Syndrome: Diagnosis, Clinical and Laboratory Manifestations, and Treatment

(2009) Hans D. Ochs et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION