408 results on '"White, Gilbert C."'
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152. Colonoscopic polypectomy in Glanzmann's thrombasthenia
153. Platelet factor 4 enhances fibrin fiber polymerization
154. The recombinant factor IX clinical investigator group’s response to Dr Haase
155. Introduction
156. Glanzmann's thrombasthenia: Report of two oral surgical cases using a new microfibrillar collagen preparation and EACA for hemostasis
157. Immunoglobulin D Myeloma and Amyloidosis: Immunochemical and Structural Studies of Bence Jones and Amyloid Fibrillar Proteins
158. Nosocomial infection rate as a function of human immunodeficiency virus type 1 status in hemophiliacs
159. DISTINCT ROLES for Rap1b In PLATELET SECRETION and INTEGRIN aIIBb3OUTSIDE-In SIGNALING
160. Definitions in Hemophilia
161. Kenneth M. Brinkhous
162. Utilization of Previously Treated Patients (PTPs), Noninfected Patients (NIPs), and Previously Untreated Patients (PUPs) in the Evaluation of New Factor VIII and Factor IX Concentrates
163. HIV-1 infection in a man homozygous for CCR5▵32
164. Human Immunodeficiency Virus (HIV) Type 1 Infection Status and In Vitro Susceptibility to HIV Infection among High-Risk HIV-I-Seronegative Hemophiliacs
165. Failure of Activated Prothrombin Complex Concentrates in a Hemophiliac With an Anti-Factor VIII Antibody
166. Mechanisms of B-cell Tolerance
167. CD40L Pathway Blockade as an Approach to Immunotherapy
168. The Incidence of Inhibitors in Hemophilia A and the Induction of Immune Tolerance
169. CD4+ T Cells Specific for Factor VIII as a Target for Specific Suppression of Inhibitor Production
170. Mechanisms of Unresponsiveness:T- And B-Cell Mediated Mechanisms of Anergy
171. Use of High Dose Factor Vila in Hemophilia Patients
172. Factor Viii Inhibitors
173. Gene Therapy for Hemophilia B: Aav-Mediated Transfer of The Gene for Coagulation Factor IX to Human Muscle
174. Factor V: Dr. Jeckyll and Mr. Hyde
175. Use of Prophylaxis to Prevent Complications of Hemophilia
176. The Transfusion-Transmitted Viruses in Blood Transfusion
177. Are Patients with Glanzmann Thrombasthenia and the Bernard-Soulier Syndrome Protected Against Atherosclerosis?
178. Factor IX activator content of normal and factor XI deficient serum
179. CHAPTER 129 - VON WILLEBRAND DISEASE: CLINICAL ASPECTS AND THERAPY
180. Chapter 71 - Gene therapy for platelet disorders
181. IVIg in the treatment of patients with factor VIII inhibitors
182. Variable (V) region-mediated control of autoreactivity to factor VIII
183. Apheresis
184. Hepatic gene therapy for hemophilia B
185. Immune tolerance to Factor VIII:The international registry data
186. Multiple mechanisms of immunologic tolerance: Novel approaches for unresponsiveness
187. The function of factor VIIa in hemophilia A: An hypothesis
188. Tolerance and intolerance to factor VIII: A clinical perspective
189. Clinical update on the use of recombinant factor VII
190. Antibodies to von Willebrand factor in von Willebrand disease
191. Structure and function of Factor VIII
192. Molecular etiology of factor VIII deficiency in hemophilia A
193. Immunoglobulin heavy chain variable region gene usage in human autoimmune diseases
194. Porcine factor VIII therapy in patients with factor VIII inhibitors
195. T-cell receptors in immune responses
196. B-cell epitopes:Fact and fiction
197. Antigen analogs as therapeutic agents
198. Factor IX:Molecular structure, epitopes, and mutations associated with inhibitor formation
199. The incidence of factor VIII inhibitors in patients with severe hemophilia A
200. Immunogenetics of the human immune response to factor VIII
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