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- Aad, G., et al.
(författare)
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- 2013
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Ingår i: Journal of High Energy Physics. - 1029-8479 .- 1126-6708. ; :1
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Tidskriftsartikel (refereegranskat)
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- Goto, Motoshi, et al.
(författare)
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Ionization of naphthalene via the Rydberg States using a femtosecond 775 nm pulse
- 2012
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Ingår i: Chemical Physics Letters. - 0009-2614. ; 522, s. 23-27
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Tidskriftsartikel (refereegranskat)abstract
- Photoelectron spectroscopic studies on naphthalene excited with a femtosecond 775 nm laser pulse reveal two ionization paths via the Rydberg states: a resonance-enhanced, non-relaxed process and one that goes through internal conversion of an undetermined intermediate. Varying the pulse duration with several hundred femtosecond causes only small change in the spectra. Compared to the ionization mechanism of anthracene, the reduced molecular size changes the ionization behavior due to a slower internal conversion rate and the presence of atomic-like Freeman resonances.
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- Guaraldi, Federica, et al.
(författare)
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Hypophysitis
- 2018. - 2
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Ingår i: Encyclopedia of Endocrine Diseases. - : Academic Press. - 9780128122006 ; , s. 325-338
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Bokkapitel (refereegranskat)
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9. |
- Guaran, Valeria, et al.
(författare)
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Association between idiopathic hearing loss and mitochondrial DNA mutations : a study on 169 hearing-impaired subjects
- 2013
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Ingår i: International Journal of Molecular Medicine. - Athen : Spandidos Publications. - 1107-3756 .- 1791-244X. ; 32:4, s. 785-794
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Tidskriftsartikel (refereegranskat)abstract
- Mutations in mitochondrial DNA (mtDNA) have been shown to be an important cause of sensorineural hearing loss (SNHL). In this study, we performed a clinical and genetic analysis of 169 hearing-impaired patients and some of their relatives suffering from idiopathic SNHL, both familial and sporadic. The analysis of four fragments of their mtDNA identified several polymorphisms, the well known pathogenic mutation, A1555G, and some novel mutations in different genes, implying changes in the aminoacidic sequence. A novel sporadic mutation in 12S rRNA (MT-RNR1), not previously reported in the literature, was found in a case of possible aminoglycoside-induced progressive deafness.
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