680 results on '"Ishii Atsushi"'
Search Results
152. SCN8A encephalopathy: Research progress and prospects
153. Transdisciplinary co-design of scientific research agendas: 40 research questions for socially relevant climate engineering research
154. Treatment with Oral ATP decreases alternating hemiplegia of childhood with de novo ATP1A3 Mutation
155. Present Status of the Compact ERL at KEK
156. The First Beam Recirculation and Beam Tuning in the Compact ERL at KEK
157. メコンデルタにおける作付体系の変化 : 水利改良との関係を中心に
158. Domestic sources of international fisheries diplomacy: A framework for analysis.
159. Somatic mosaic deletions involving <italic>SCN1A</italic> cause Dravet syndrome.
160. KCNQ2 abnormality in BECTS: Benign childhood epilepsy with centrotemporal spikes following benign neonatal seizures resulting from a mutation of KCNQ2
161. Radiolarian Assemblage-zones in the Jurassic and Cretaceous Sequence in the Kanto Mountains, Central Japan
162. Retigabine, a Kv7.2/Kv7.3-Channel Opener, Attenuates Drug-Induced Seizures in Knock-In Mice Harboring Kcnq2 Mutations
163. Strip Warpage Behavior and Mechanism in Single Roll Driven Rolling
164. Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes
165. A 60GHz-Band High-Efficiency Antenna with a Thick Resin Layer and Differentially Fed through a Hole in a Silicon Chip
166. The Markov theorems for spatial graphs and handlebody-knots with Y-orientations
167. Ring Chromosome 20 Syndrome and Epilepsy
168. A case of recurrent encephalopathy with SCN2A missense mutation
169. Phenotypes of children with 20q13.3 microdeletion affecting KCNQ2 and CHRNA4
170. Interventions for body weight reduction in obese patients during short consultations: an open-label randomized controlled trial in the Japanese primary care setting
171. Clinical and genetic features of acute encephalopathy in children taking theophylline
172. Single Nucleotide Variations in CLCN6 Identified in Patients with Benign Partial Epilepsies in Infancy and/or Febrile Seizures
173. Power Coupler Development for ERL Main LINAC in Japan
174. Detection of human adenovirus hexon antigen using carbon nanotube sensors
175. Japan and the whaling issue: A viewpoint based on a review of “Whaling in Japan: Power, politics, and diplomacy” by Jun Morikawa
176. Different links with the same Links-Gould invariant
177. Effect of CYP2C19 polymorphisms on stiripentol administration in Japanese cases of Dravet syndrome
178. The g.841G>C SNP ofFASNgene is associated with fatty acid composition in beef cattle
179. Strip Warpage Behavior and Mechanism in Single Roll Driven Rolling
180. Knotted handle decomposing spheres for handlebody-knots
181. バングラデシュにおける河川堤防の機能と保全に関する調査研究
182. Exacerbation of Benign Familial Neonatal Epilepsy Induced by Massive Doses of Phenobarbital and Midazolam
183. Path Dependence and Paradigm Shift: How Cetacean Scientists Learned to Develop Management Procedures that Survived the Controversial Whaling Regime
184. A novel SCN1A mutation in a cytoplasmic loop in intractable juvenile myoclonic epilepsy without febrile seizures
185. Handlebody-knot invariants derived from unimodular Hopf algebras
186. Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC)
187. Genotype–phenotype correlations in alternating hemiplegia of childhood
188. MEDIA REPRESENTATIONS AND GOVERNANCE OF CCS
189. A recurrent KCNT1 mutation in two sporadic cases with malignant migrating partial seizures in infancy
190. Insights from Global Environmental Governance
191. Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism
192. Identification of quantitative trait loci affecting economic traits based on divergently selected genomic regions between beef and dairy cattle
193. Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis
194. Influence of STI stress on leakage current in buried P-N junction
195. Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot study
196. Genome-wide association study for fatty acid composition in Japanese Black cattle
197. メコンデルタにおける作付体系の変化 : 水利改良との関係を中心に
198. A pH sensor based on electric properties of nanotubes on a glass substrate
199. Ultrasensitive detection of organophosphate insecticides by carbon nanotube field-effect transistor
200. Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome.
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