412 results on '"Carrara F"'
Search Results
102. Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases
103. Clinical and molecular findings in the first identified Italian family with dentatorubral-pallidoluysian atrophy
104. Clinical and molecular features of mitochondrial DNA depletion syndromes
105. Radio-frequency front-end for 5 GHz wireless local area network transceivers
106. Low-power RF circuits for multi-standard WLAN transceivers
107. Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants
108. Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy
109. Design methodology for the optimization of transformer-loaded RF circuits
110. High-dynamic-range VGA with temperature compensation and linear-in-dB gain control
111. A silicon bipolar transmitter front-end for 802.11a and HIPERLAN2 wireless LANs
112. A VSWR-protected silicon bipolar RF power amplifier with soft-slope power control
113. Clinical and molecular findings in children with complex I deficiency
114. High-dynamic-range variable gain amplifier with temperature compensation and linear-in-decibel gain control
115. High-efficiency reconfigurable RF transmitter for wireless sensor network applications.
116. Mutations of ANT1 , Twinkle , and POLG1 in sporadic progressive external ophthalmoplegia (PEO)
117. A 2.4-GHz 24-dBm SOI CMOS power amplifier with on-chip tunable matching network for enhanced efficiency in back-off.
118. A stage-bypass SOI-CMOS switch for multi-mode multi-band applications.
119. A 900-MHz RFID system with TAG-antenna magnetically-coupled to the die.
120. A high-resolution 24-dBm Digitally-Controlled CMOS PA for multi-Standard RF polar transmitters.
121. Fast Peak Detector with Improved Accuracy and Linearity for High-Frequency Waveform Processing.
122. A 3W 55% PAE CMOS PA with Closed-Loop 20:1 VSWR Protection.
123. Degradation Mechanisms in CMOS Power Amplifiers Subject to Radio-Frequency Stress and Comparison to the DC Case.
124. NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy
125. Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentations
126. A VSWR-rugged silicon bipolar RF power amplifier.
127. The transformer characteristic resistance and its application to the design of rf circuits.
128. A soft-slope output power control circuit for rf power amplifiers.
129. The transformer characteristic resistance and its application to the performance analysis of silicon integrated transformers.
130. A high performance silicon bipolar monolithic RF linear power amplifier for W-LAN IEEE 802.11g applications.
131. A 5-GHz silicon bipolar transmitter front-end for wireless LAN applications.
132. A low cost power amplifier for 5-GHz W-LAN applications (invited paper).
133. A silicon bipolar technology for high-efficiency power applications up to C-band.
134. Large-signal characterization and modeling of a silicon bipolar technology for high-efficiency power applications up to C-band.
135. Wide-bandwidth fully integrated Cartesian feedback transmitter.
136. Epileptic phenotypes associated with mitochondrial disorders
137. High performance silicon bipolar power amplifier for 1.8 GHz applications.
138. ChemInform Abstract: Stereoselective Thioglycose Synthesis. Part 17. Synthesis of Sulfur‐ Linked Analogues of Nigerose, Laminarabiose, Laminaratriose, Gentiobiose, Gentiotriose, and Laminaran Trisaccharide Y.
139. La gamme Solissime d’aciers prélaqués pour le bâtiment
140. Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype
141. Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy.
142. Glomerular hyperfiltration and renal disease progression in type 2 diabetes.
143. Primary carnitine deficiency
144. Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants.
145. Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes
146. Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.
147. A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients.
148. A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation.
149. Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases.
150. Clinical and molecular findings in the first identified Italian family with dentatorubral-pallidoluysian atrophy.
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