Antti Aalto
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Explore the profile of Antti Aalto including associated specialties, affiliations and a list of published articles.
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7
Citations
44
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Recent Articles
1.
Malmivaara K, Polkki M, Prami T, Raittinen P, Heikkila E, Aalto A, et al.
Heliyon
. 2024 Jul;
10(13):e33439.
PMID: 39040318
Background: Knowledge of prevalence and epidemiology of cystic fibrosis (CF) and healthcare resource use among Finnish people with CF is incomplete. Methods: We conducted a population-based matched cohort study using...
2.
Saleh A, Aalto A, Ryczkowski P, Genty G, Toivonen J
Opt Lett
. 2019 Aug;
44(17):4223-4226.
PMID: 31465367
We developed a short-range light detection and ranging system using a supercontinuum (SC) source spectrally tailored to cover the ro-vibrational transition energies of desired components of a flue gas. The...
3.
Mikkonen T, Amiot C, Aalto A, Patokoski K, Genty G, Toivonen J
Opt Lett
. 2018 Oct;
43(20):5094-5097.
PMID: 30320828
We demonstrate cantilever-enhanced photoacoustic spectroscopy in the mid-infrared using a supercontinuum source. The approach is broadband and allows for higher photoacoustic signal intensity and an enhanced signal-to-noise ratio as compared...
4.
Aalto A, Genty G, Laurila T, Toivonen J
Opt Express
. 2015 Sep;
23(19):25225-34.
PMID: 26406720
We investigate incoherent broadband cavity enhanced absorption spectroscopy using a tailored supercontinuum source. By tailoring the supercontinuum spectrum to match the high reflectivity bandwidth of the mirrors, we achieve an...
5.
Aalto A, Genty G, Toivonen J
Opt Express
. 2010 Feb;
18(2):1234-9.
PMID: 20173946
We study experimentally the statistical fluctuations observed in a supercontinuum generated in the normal dispersion regime through cascaded stimulated Raman scattering. Specifically, we show that the statistical distribution of shot-to-shot...
6.
Joensuu T, Kuronen M, Alakurtti K, Tegelberg S, Hakala P, Aalto A, et al.
Eur J Hum Genet
. 2006 Sep;
15(2):185-93.
PMID: 17003839
Progressive myoclonus epilepsy of Unverricht-Lundborg type (EPM1) is an autosomal recessive neurodegenerative disorder caused by mutations in the cystatin B gene (CSTB) that encodes an inhibitor of several lysosomal cathepsins....
7.
Lonka L, Aalto A, Kopra O, Kuronen M, Kokaia Z, Saarma M, et al.
BMC Neurosci
. 2005 Apr;
6:27.
PMID: 15826318
Background: The neuronal ceroid lipofuscinoses (NCLs) are a group of inherited neurodegenerative disorders characterized by accumulation of autofluorescent material in many tissues, especially in neurons. Mutations in the CLN8 gene,...