748 results on '"Ebers, George"'
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152. Faculty Opinions recommendation of Disability and T2 MRI lesions: a 20-year follow-up of patients with relapse onset of multiple sclerosis.
153. Reducing the probability of false positive research findings by pre-publication validation – Experience with a large multiple sclerosis database
154. No Effect of Birth Weight on the Risk of Multiple Sclerosis
155. Parental transmission of HLA-DRB1*15 in multiple sclerosis
156. The Inheritance of Resistance Alleles in Multiple Sclerosis
157. Multiple sclerosis: the environment and causation
158. Clustering of autoimmune disease in families at high risk for multiple sclerosis?
159. Multiple Sclerosis: Critical Review of the Evidence for each Question
160. PRKCA and Multiple Sclerosis: Association in Two Independent Populations
161. Birth order, infection in early life, and multiple sclerosis – Authors' reply
162. A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis
163. Suppressor Alleles in Multiple Sclerosis: Inheritance and Interactions
164. Timing of birth and risk of multiple sclerosis: population based study
165. Natural history of primary progressive multiple sclerosis
166. Quote by Ebers, George on Friends and Friendship
167. Progress in deciphering the genetics of multiple sclerosis
168. Microchimerism in autoimmunity and transplantation: potential relevance to multiple sclerosis
169. Interferon in relapsing-remitting multiple sclerosis
170. Evidence of Linkage with HLA-DR in DRB1*15-Negative Families with Multiple Sclerosis
171. Reply
172. MRI: measure of efficacy
173. Book Review Multiple Sclerosis Therapeutics Edited by Richard A. Rudick and Donald E. Goodkin. 574 pp. London, Martin Dunitz, 1999. £79.95. 1-85317-812-8
174. Modelling multiple sclerosis
175. Randomised double-blind placebo-controlled study of interferon β-1a in relapsing/remitting multiple sclerosis
176. Genetics of Multiple Sclerosis
177. A full genome search in multiple sclerosis
178. Genetics of Multiple Sclerosis
179. Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p
180. X Chromosome Inactivation Patterns Correlate with Fetal-Placental Anatomy in Monozygotic Twin Pairs: Implications for Immune Relatedness and Concordance for Autoimmunity
181. The role of genetic factors in multiple sclerosis susceptibility
182. Cyclophosphamide and MS
183. Genetics and multiple sclerosis: An overview
184. Interferon β for secondary progressive multiple sclerosis: a systematic review.
185. Multiple Sclerosis: New Insights From Old Tools
186. Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)
187. The Geographic Distribution of Multiple Sclerosis: A Review
188. Clinicopathological features of primary lateral sclerosis are different from amyotrophic lateral sclerosis
189. Robert Whytt, Benjamin Franklin, and the first probable case of multiple sclerosis.
190. Vitamin D receptor binding, chromatin states and association with multiple sclerosis.
191. Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.
192. Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis.
193. Relationship between early clinical characteristics and long term disability outcomes: 16 year cohort study (follow-up) of the pivotal interferon b-1b trial in multiple sclerosis.
194. Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences.
195. Rare variants in the CYP27B1 gene are associated with multiple sclerosis.
196. Geography of hospital admissions for multiple sclerosis in England and comparison with the geography of hospital admissions for infectious mononucleosis: a descriptive study.
197. Role of the HLA System in the Association Between Multiple Sclerosis and Infectious Mononucleosis.
198. Lockhart Clarke's contribution to the description of amyotrophic lateral sclerosis.
199. A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
200. Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis.
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