- ►pnas.org [PDF] AS Levin, LE Spitler, DP Stites, HH … - Proceedings of the …, 1970 - National Acad Sciences Page 1. Proceedings of the National Academy of Sciences Vol. 67, No. 2, pp. 821-828, October
1970 Wiskott-Aldrich Syndrome, A Genetically Determined Cellular Immunologic Deficiency:
Clinical and Laboratory Responses to Therapy with Transfer Factor* ... Cited by 105 - Related articles - All 7 versions
- ►nih.gov [PDF] LE Spitler, AS Levin, DP Stites, HH … - Journal of Clinical …, 1972 - pubmedcentral.nih.gov A BST R A C T 12 patienits witlh Wiskott-Aldriclh syni- (irome were treated with therapeutic doses
of transfer fac- tor in an attempt to induce cellular immunity. Clinical imiiprovement was noted
after transfer factor therapy in 7 of the 12 patients treated. Because this disease has a ... Cited by 103 - Related articles - All 5 versions
KP Heidelberger, DP Legolvan, IV … - CA A Cancer Journal for … - interscience.wiley.com A case of Wiskott-Aldrich Syndrome with survival to nineteen-years old is reported. The patient
developed reticulum cell sarcoma primary in the brain, which was biopsied and treated with irradiation
and chemotherapy. When the patient expired 4 1/2 months postoperatively, no tumor was ... Cited by 29 - Related articles - All 2 versions
C Someryille, KD Forsyth - Pediatric Allergy and Immunology, 1993 - interscience.wiley.com Wiskott Aldrich syndrome, a combined cellular and humoral X-linked immunodeficiency, is generally
considered to be rare. The aim of this study was to ascertain the true prevalence in the paediatric
population in Western Australia, describe the clinical features, and summarise the current ... Cited by 11 - Related articles - BL Direct - All 2 versions
AD Ormerod, AY Finlay, AG Knight, N Mathews, … - Br J …, 1983 - interscience.wiley.com It is also possible that your web browser is not configured or not able to display style sheets.
In this case, although the visual presentation will be degraded, the site should continue to be
functional. We recommend using the latest version of Microsoft or Mozilla web browser to ... Cited by 10 - Related articles - All 2 versions
DS CHENG, TM COSGRIFF, M … - The American Journal of …, 1981 - journals.lww.com Case Report Long-Term Survival in Wiskott-Aldrich Syndrome: Case Report and Literature Review
DAVID S. CHENG. MD THOMAS M. COSGRIFF. MD MISTUSO KITAHARA, MD Abstract: The
case reported concerns a 29-year-old man who was seen because of clinical and ... Cited by 5 - Related articles - All 2 versions
AM Mauer - Journal of Investigative Dermatology, 1973 - nature.com Baldini, M, Kim, B, Steiner, M, Kuramoto, A, Okuma, M, Otridge, BW: Metabolic platelet detect
in the Wiskott-Aldrich syndrome. Pediatr. Res 1969 3: 377–378. ... Canales, L, Mauer, AM:
Sex-linked hereditary thrombocytopema as a variant of Wiskott-Aldrich syndrome. N. ... Cited by 4 - Related articles - All 2 versions
VA MARINKOVICH - Clinical & Experimental Allergy, 1972 - interscience.wiley.com A comparison of serum immunoglobulin levels in children with Wiskott-Aldrich Syndrotne
(WAS) and in children with chronic eczema demonstrated lower IgM, higher IgA and lower IgG
concentrations in WAS patients. Seven patients with WAS were studied for in vitro ... Cited by 3 - Related articles - All 2 versions
AL Horwich, MR Seashore, JM Dwyer - Archives of Internal …, 1984 - archinte.highwire.org Although the factor levels in this case reflected disease activity4 and was transient, this was not
so in the patient described herein. Indeed, our patient was thought to have an inherited factor
XII deficiency. Factor XII deficiency was demonstrated during a period of 16 months, ... Cited by 2 - Related articles - All 6 versions
