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252. FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study.

253. A comparison between SSMF and large-Aeff Pure-Silica core fiber for Ultra Long-Haul 100G transmission

255. Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy

256. Secondary ion mass spectrometry round-robin study for relative sensitivity factors in gallium arsenide

258. Role of multifunctional transcription factor TFII-I and putative tumour suppressor DBC1 in cell cycle and DNA double strand damage repair

260. P.5.12 A mutation in TNPO3 causes LGMD1F and characteristic nuclear pathology

272. Extensive Fiber Comparison and GN-model Validation in Uncompensated Links using DAC-generated Nyquist-WDM PM-16QAM Channels

274. Mitochondrial disease mimicking Charcot-Marie Tooth disease

280. UBQLN2 Mutations in ALS and ALS/Dementia: A Genetic, Functional and Histopathological Analysis (S05.006)

293. Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype

297. New tools to reduce non-responders and to select candidates for CRT

298. NMR/NQR and Specific Heat Studies of Iron Pnictide Superconductor KFe2As2

299. Pressure and K doping induced superconductivity in BaFe2As2

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