Cerebral Vasculitis in X-linked Lymphoproliferative Disease Cured by Matched Unrelated Cord Blood Transplant

Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene

(2014) B. Tóth et al.   JOURNAL OF CLINICAL IMMUNOLOGY

XLP: Clinical Features and Molecular Etiology due to Mutations in SH2D1A Encoding SAP

(2014) Stuart G Tangye   JOURNAL OF CLINICAL IMMUNOLOGY

Lymphoma and cerebral vasculitis in association with X-linked lymphoproliferative disease

(2013) Jia Zhu et al.   Chinese Journal of Cancer

Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management

(2011) C. Gholam et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY

Molecular Pathogenesis of EBV Susceptibility in XLP as Revealed by Analysis of Female Carriers with Heterozygous Expression of SAP

(2011) Umaimainthan Palendira et al.   PLOS BIOLOGY

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

(2010) J. P. Schmid et al.   BLOOD

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease

(2010) C. Booth et al.   BLOOD

Lymphocytic vasculitis involving the central nervous system occurs in patients with X-linked lymphoproliferative disease in the absence of Epstein-Barr virus infection

(2009) Kawsar R. Talaat et al.   PEDIATRIC BLOOD & CANCER