- ►hematologylibrary.org [PDF] RJ Charles, KM Sabo, PG Kidd, JL Abkowitz - Blood, 1996 - bloodjournal.hematologylibrary.org . reserved Hematology; all rights Copyright 2007 by The American Society of
Suite 200, Washington DC 20036. semimonthly by the American Society of
Hematology, 1900 M St, NW, Blood (print ISSN 0006-4971, online ISSN ... Cited by 105 - Related articles - BL Direct - All 4 versions
- ►bloodjournal.org M Morra, O Silander, S Calpe, M Choi, H … - Blood, 2001 - Am Soc Hematology The gene responsible for the disease has been cloned and named SAP (for
SLAM-associated protein) or SH2D1A. 8-10 The human and mouse SH2D1A genes
consist of 4 exons and 3 introns spanning approximately 25 kilobase (kb). 8 ... Cited by 78 - Related articles - BL Direct - All 7 versions
SS Ammus, AA Yunis - American journal of hematology, 1987 - ncbi.nlm.nih.gov 1: Am J Hematol. 1987 Mar;24(3):311-26. Acquired pure red cell aplasia.
Ammus SS, Yunis AA. Publication Types: Review. Mesh Terms ... Cited by 44 - Related articles - All 3 versions
DT Purtilo, HL Grierson, JR Davis, M Okano - Fetal & Pediatric Pathology, 1991 - informahealthcare.com 0 Although X-linked lymphoproliferative disease (XLP) is rare (1-2 males per 1 X
106), it serves as a model for discerning diverse diseases caused by Epstein-Ban
virus (EBV) ranging from agamnaglobu- linemia to fatal infectious ... Cited by 34 - Related articles - All 3 versions
DT Purtilo, HL Grierson, H Ochs, J Skare - The American Journal of Medicine, 1989 - Elsevier : Concordance for detection of affected males was 100% when linkage analysis
using DXS42 and DXS37 DNA probes and antibody responses to challenge with
bacteriophage ΦX174 were both determined. Most affected males showing IgG ... Cited by 31 - Related articles - All 7 versions
- ►bloodjournal.org R Sumazaki, H Kanegane, M Osaki, T … - Blood, 2001 - Am Soc Hematology X-linked lymphoproliferative disease (XLP, MIM 308240) is an inherited
immunodeficiency characterized by extreme vulnerability to Epstein-Barr virus
(EBV). 1 About two-thirds of the patients develop fatal infectious ... Cited by 29 - Related articles - BL Direct - All 7 versions
DT Purtilo - Springer seminars in immunopathology, 1991 - Springer X-linked lymphoproliferative disease (XLP) is characterized by an exquisite
vulnerability to Epstein-Barr virus (EBV) [42-56]. EBV was etiologically linked
with African Burkitt lymphoma (BL), nasopharyngeal carcinoma (NPC), and ... Cited by 17 - Related articles - All 3 versions
- ►nih.gov [PDF] F Pandolfi, L Trentin, JE San Martin, JT Wong … - Clinical and Experimental Immunology, 1992 - pubmedcentral.nih.gov SUMMARY T lymphocyte regulation of immunoglobulin production may be abnormal in
some patients with common variable immunodeficiency (CVI). Phenotypic analysis
ofperipheral blood T lymphocytes from nine patients with CVI was conducted ... Cited by 15 - Related articles - All 4 versions
EF Jaffe, MC Lejtenyi, FJD Noya, BD Mazer - Immunology and Allergy Clinics of North America, 2001 - Elsevier These cases, including primary B-cell defects and most combined immune
deficiencies, are generally caused by genetic defects. There is, however, a
heterogeneous group of disorders known as acquired or secondary ... Cited by 4 - Related articles - BL Direct - All 6 versions
JF JONES, B KATZ - Herpesvirus infections, 1994 - books.google.com Epstein-Barr Virus Infections in Normal and Immunosuppressed Patients JAMES F.
JONES National Jewish Center for Immunology and Respiratory Medicine and
University of Colorado School of Medicine Denver, Colorado BEN Z. KATZ ... Cited by 4 - Related articles - BL Direct
