473 results on '"Magariello A"'
Search Results
152. A novel locus for Autosomal Dominant Distal Motor Neuronopathy maps to chromosome 4q-ter
153. Charcot-Marie-Tooth X-linked: five novel mutations in Italian patients
154. Two novel NOTCH3 mutations not involving cysteine residues in CADASIL patients
155. Genetically-dependent modulation of serotonergic inactivation in the human ventrolateral prefrontal cortex
156. Angiogenin gene and Amyotrophic Lateral Sclerosis in Southern Italy
157. Spastin gene mutation in italian patients with pure and complicated forms of spastic paraplegia
158. Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity
159. A novel NOTCH3 gene mutation in a patient with CADASIL from Southern Italy
160. Ventro-Lateral Prefrontal activity during working-memory processing is modulated by Monoamine oxidase-A genetic variation
161. Influence of functional polymorphism in MAO-A on neural network responsible of spatial working memory
162. Angiogenin Gene and Amyotrophic Lateral Sclerosis in Southern Italy
163. Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathy
164. Monoamine Oxidase-A genetic variation and the medial temporal lobe response to affective stimuli
165. DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES:THE ROLE OF MAGNETIC RESONANCE IMAGING IN THE NOTCH3 GENE SCREENING
166. Neurofibromatosis type2 (NF2) in children under 1 year of age: a clinical and molecular study
167. HNPP Due To A Novel Frameshift Mutation Of The PMP22 Gene
168. Il Ruolo Della Rm Nello Screening Sul Gene Notch3: Distinguere I Soggetti Cadasil Apparentemente Sporadici Da Altre Leucoencefalopatie
169. Ricerca di mutazioni nel gene jag1 e loro possibile implicazione nella modulazione di fenotipi simili al Cadasil
170. A novel Notch3 gene mutation in a patient with CADASIL from Southern Italy
171. Nuove Mutazioni Del Gene Mecp2 Identificate In Pazienti Affetti Da Sindrome Di Rett Provenienti Dallitalia Meridionale
172. Molecular testing in Neurofibromatosis type 1 (NF1): mutational spectrum, patterns of recurrence and correlation with clinical features in Italy
173. Nuove mutazioni identificate nel gene della spastina in soggetti affetti da Paraplegia Spastica Ereditaria
174. HNPP due to a novel frameshift mutation of PMP22 gene
175. Could the expression of Jagged1 gene mutations play a role in modulatine a CADASIL-like phenotype?
176. INDIVIDUAZIONE DI UN NUOVO LOCUS SUL CROMOSOMA 4 RESPONSABILE DI NEUROPATIA MOTORIA DISTALE AUTOSOMICA DOMINANTE
177. A Clinical And Molecular Study In Children Under 1 Year Of Age Affected By Neurofibromatosis Type 2
178. Two novel Notch3 mutations not involving cysteine residues in CADASIL patients
179. Novel Mecp2 Mutations Identified In Patients From Southern Italy With Rett syndrome
180. Due nuove mutazioni non coinvolgenti residui di cisteina in pazienti affetti da CADASIL
181. ANALYSIS OF SMN1 GENE COPY NUMBER TO DETECT SMA HEALTH CARRIERS IN SOUTHERN ITALY POPULATION
182. Molecular Testing in Neurofibromatosis type 1 (NF1) mutational spectrum, patterns of reccurrence and correlation with clinical features in Italy
183. Two Novel Cysteine-Sparing Notch3 Mutations In Patients With CADASIL
184. DISTINGUISHING APPARENTLY SPORADIC CADASIL FROM OTHER LEUCOENCEPHALOPATHIES: THE ROLE OF MRI IN THE NOTCH3 GENE SCREENING
185. Neurofibromatosis Type 2 (Nf2) In Children Under 1 Year Of Age: A Clinical And Molecular Study
186. SUGGESTIVE EVIDENCE FOR LINKAGE TO CHROMOSOME 4qter FOR AUTOSOMAL DOMINANT DISTAL MOTOR NEURONOPATHY
187. SLA sporadica e mutazioni del gene VAPB nellItalia meridionale
188. Assenza di correlazione tra sclerosi multipla familiare (SM) e mutazioni nel gene eIF2B5
189. Notch3 screening in patients with sporadic leucoencephalopathy
190. Sporadic ALS and VAPB gene mutations in Southern Italy
191. Tre nuove mutazioni nel gene SPG4 identificate in pazienti affetti da paraparesi spastica ereditaria
192. Absence of heart abnormalities in subjects not carryng large NF1 gene deletions
193. Three novel mutations in CX32 gene detected by DHPLC mutation analysis
194. Mutational analysis in NF1 patients screened for heart abnormalities
195. MAO-A genetic variations influence the prefrontal cortical activity associated to a response inhibition task
196. Molecular testing in Neurofibromatosis type 1 (NF1): Mutational spectrum, patterns of recurrence and correlation with clinical features in Italy
197. Molecular testing in Neurofibromatosis type 1 (NF1): Mutational spectrum, patterns of recurrence and correlation with clinical features in Italy
198. New spastin (SPG4) mutations in patients with Hereditary Spastic Paraplegia
199. Cinque nuove mutazioni nel gene Cx32 rivelate mediante DHPLC
200. Five novel mutations in CX32 gene detected by DHPLC mutation analysis
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